TWI482844B - Liquid crystal composition, liquid crystal display element using same, and liquid crystal display using same - Google Patents

Description

Liquid crystal composition, liquid crystal display element, and liquid crystal display

The present invention relates to a nematic liquid crystal composition which exhibits a positive dielectric constant anisotropy (??) as a liquid crystal display material, a liquid crystal display element using the same, and a liquid crystal display.

The liquid crystal display element is represented by a timepiece or a desktop electronic computer, and is used in various measuring apparatuses, automobile panels, word processors, electronic notebooks, printers, computers, televisions, clocks, advertisement display boards, and the like. Examples of the liquid crystal display method include a TN (twisted nematic) type, an STN (super twisted nematic) type, a vertical alignment type using a TFT (thin film transistor), or an IPS (transverse electric field switching) type. The liquid crystal composition used in these liquid crystal display elements is required to exhibit stability in terms of moisture, air, heat, light, etc., and to display a liquid crystal phase in a wide temperature range as wide as possible around a room temperature. Low viscosity and low drive voltage. Further, in order to optimize the dielectric anisotropy (Δε) or refractive index anisotropy (Δn) which are most suitable for each display element, the liquid crystal composition is composed of several kinds to several tens of kinds of compounds. Composition.

In a vertical alignment (VA) type display, a liquid crystal composition having a negative Δ ε is used, and in a horizontal alignment type display such as a TN type, an STN type, or an IPS (transverse electric field switching) type, a liquid crystal composition having a positive Δ ε is used. Things. Further, it has been reported that when the voltage is not applied, the liquid crystal composition having positive Δ ε is vertically aligned, and the driving mode is displayed by applying a lateral electric field, and the necessity of the liquid crystal composition having positive Δ ε is further increased. . On the other hand, in all driving methods, low voltage driving, fast response, and a wide operating temperature range are required. That is, it is required that Δε is positive and the absolute value is large, the viscosity (η) is small, and the high nematic phase-isotropic liquid phase transition temperature (Tni) is required. In addition, in order to set Δn×d of the product of Δn and the cell gap (d) to a predetermined value, it is necessary to adjust the Δn of the liquid crystal composition to the gap of the liquid crystal layer and adjust it to an appropriate range. Further, when a liquid crystal display element is applied to a television or the like, a liquid crystal composition having a small rotational viscosity (γ ₁ ) is required because of importance of rapid reactivity.

In the configuration of the liquid crystal composition which is intended to be a rapid reactivity, for example, a compound represented by the following formula (A-1) or the following formula (A-2) which exhibits a liquid crystal compound having a positive combination Δε and Δ are disclosed. ε is a liquid crystal composition used for a compound represented by the following formula (B) which is a neutral liquid crystal compound. These liquid crystal compositions are characterized in that the liquid crystal compound having a positive Δ ε has a -CF ₂ O- structure, and the liquid crystal compound having a negative Δ ε has an alkenyl group. These characteristics are widely known in the field of the liquid crystal composition (see Patent Documents 1 to 4).

On the other hand, the use of the liquid crystal display element has been expanded, and the use method and manufacturing method have also been greatly changed. In order to cope with such changes, it is required to optimize the characteristics other than the basic physical property values. In other words, a liquid crystal display element using a liquid crystal composition has been widely used, such as a VA type or an IPS type, and a display element having a size of 50 or more and a very large size has been put into practical use. With the increase in the size of the substrate, the method of injecting the liquid crystal composition into the substrate has become the mainstream of the injection method from the conventional vacuum injection method to the ODF (One Drop Fill) method. However, when the liquid crystal composition is dropped onto the substrate, the problem that the drop marks cause a decrease in display quality is revealed. Further, in the process of the liquid crystal display element of the ODF method, it is necessary to drip the optimum amount of liquid crystal in accordance with the size of the liquid crystal display element. When the deviation of the amount of dripping is larger than the optimum value, the balance of the refractive index or the driving electric field of the liquid crystal display element which is designed in advance may collapse, and display defects such as spots or poor contrast may occur. In particular, in the small-sized liquid crystal display elements which are widely used in recent popular smart phones, since the optimum liquid crystal dropping amount is a small amount, it is difficult to control the offset with the optimum value within a certain range. Therefore, in order to maintain high liquid crystal display In the liquid crystal composition, for example, it is necessary to receive a drastic pressure change or a smear in the dripping device which occurs when the liquid crystal is dropped, and it is possible to continuously drip continuously for a long period of time.

In the liquid crystal composition used for the liquid crystal display device driven by the active matrix driven by the TFT element or the like, it is required to maintain the characteristics and performance required for the liquid crystal display element while maintaining rapid reaction performance, etc., in addition to the high ratio that has been emphasized in the past. The development of a method of manufacturing a liquid crystal display element is also considered for the resistance value, the high voltage holding ratio, and the stability of the stimulus other than light or heat.

[Previous Technical Literature] [Patent Literature]

[Patent Document 1] Japanese Patent Laid-Open Publication No. 2008-037918

[Patent Document 2] Japanese Patent Laid-Open Publication No. 2008-038018

[Patent Document 3] Japanese Laid-Open Patent Publication No. 2010-275390

[Patent Document 4] Japanese Patent Publication No. 2011-052120

The problem to be solved by the present invention is to provide a liquid crystal phase having a wide temperature range, which is small in viscosity, good in solubility at low temperatures, high in specific resistance or voltage retention, stable in heat or light, and difficult to cause marks or dripping marks. In the case of poor display, a liquid crystal composition having a positive Δ ε of a liquid crystal display element excellent in display quality and a liquid crystal display element using the liquid crystal composition can be produced with high yield.

The present inventors have examined various liquid crystal compounds and various chemical substances, and found that the above problems can be solved by combining specific liquid crystal compounds, and finally completed the present invention. That is, the first aspect of the present invention is the liquid crystal composition below, the second aspect of the present invention is the liquid crystal element below, and the third aspect of the present invention is the liquid crystal display below.

[1] A liquid crystal composition containing any one or two or more of the compounds represented by the following formula (i), and containing any one or two of the compounds represented by the following formula (ii) More than one kind, (wherein R ^11a and R ^21a each independently represent an alkyl group having 1 to 8 carbon atoms, and one of the alkyl groups or two or more non-adjacent-CH ₂ - groups may independently be -CH =CH-, -C≡C-, -O-, -CO-, -COO- or -OCO-, wherein one or more hydrogen atoms in the alkyl group are each independently a fluorine atom or Substituted with a chlorine atom, m ¹¹ represents 1 or 2, and A ¹¹ represents a trans-1,4-cyclohexylene group or a 1,4-phenylene group in which a hydrogen atom may be substituted by a fluorine atom or a chlorine atom, but when m ¹¹ is 1 When A ¹¹ represents a 1,4-phenylene group in which a hydrogen atom may be substituted by a fluorine atom or a chlorine atom, when m ¹¹ is 2, the plural A ¹¹ groups may be the same or different, but at least one of them may represent a hydrogen atom. a 1,4-phenyl group substituted by a fluorine atom or a chlorine atom, X ¹¹ represents a hydrogen atom, a fluorine atom or a chlorine atom, and X ¹² represents a hydrogen atom, a fluorine atom, a chlorine atom, a cyano group, -CF ₃ or -OCF ₃ m ²¹ represents 0 or 1, X ²¹ , X ²² , X ²³ and X ²⁴ each independently represent a hydrogen atom, a fluorine atom or a chlorine atom, and X ²⁵ represents a hydrogen atom, a fluorine atom, a chlorine atom, a cyano group, -CF ₃ Or -OCF ₃ ).

[2] The liquid crystal composition according to the above [1], wherein m ¹¹ of the above formula (i) is 2.

[3] The liquid crystal composition according to the above [1] or [2], which contains two or more compounds represented by the above formula (i).

[4] The liquid crystal composition according to any one of the above [1] to [3], which contains two or more compounds represented by the above formula (ii).

[5] The liquid crystal composition according to any one of the above [1] to [4], which contains a compound represented by the following formula (L).

(wherein R ^L1 and R ^L2 each independently represent an alkyl group having 1 to 8 carbon atoms, and one of the alkyl groups or two or more non-adjacent-CH ₂ - groups may independently be -CH =CH-, -C≡C-, -O-, -CO-, -COO- or -OCO-substitution, OL means 0, 1, 2 or 3, B ^L1 , B ^L2 and B ^L3 are each independently represented Free (a) 1,4-cyclohexylene (one -CH ₂ - or two or more -CH ₂ - which are not adjacent in this group may be substituted into -O-) and (b) 1,4 - a group in a group consisting of a phenyl group (one -CH= or a non-contiguous two or more -CH= can be substituted into -N=), the above-mentioned group (a), One or two or more hydrogen atoms in the group (b) may be independently substituted by a cyano group, a fluorine atom or a chlorine atom, and L ^L1 and L ^L2 each independently represent a single bond, -CH ₂ CH ₂ -, - (CH ₂ ) ₄ -, -OCH ₂ -, -CH ₂ O-, -COO-, -OCO-, -OCF ₂ -, -CF ₂ O-, -CH=NN=CH-, -CH=CH- , -CF=CF- or -C≡C-, when OL is 2 or 3 and L ^L2 is plural, they may be the same or different. When OL is 2 or 3 and B ^L3 is plural, Etc. can be the same or different).

[6] The liquid crystal composition according to any one of the above [1] to [5], which contains a compound represented by the following formula (M), (wherein R ^M1 represents an alkyl group having 1 to 8 carbon atoms, and one of the alkyl groups or two or more non-adjacent -CH ₂ - groups may independently be -CH=CH-, -C ≡C-, -O-, -CO-, -COO- or -OCO-substituted, PM represents 0, 1, 2, 3 or 4, and C ^M1 and C ^M2 are each independently selected from (d) 1, 4 - a cyclohexyl group (one -CH ₂ - or two or more -CH ₂ - which are not adjacent in this group may be substituted into -O- or -S-) and (e) 1,4-phenylene a group in the group consisting of one (CH============================================================================ One or more hydrogen atoms in each of them may be independently substituted by a cyano group, a fluorine atom or a chlorine atom, and K ^M1 and K ^M2 each independently represent a single bond, -CH ₂ CH ₂ -, -(CH _{2 ) 4} -, -OCH ₂ -, -CH ₂ O-, -OCF ₂ -, -CF ₂ O-, -COO-, -OCO- or -C≡C-, when PM is 2, 3 or 4 and K ^{When the} plural of ^M1 is present, they may be the same or different. When PM is 2, 3 or 4 and the complex of C ^M2 is present, they may be the same or different, and X ^M1 and X ^M3 each independently represent a hydrogen atom, a chlorine atom or a fluorine atom, X ^M2 represents a hydrogen atom, a fluorine atom, a chlorine atom , cyano, trifluoromethyl, fluoromethoxy, difluoromethoxy, trifluoromethoxy or 2,2,2-trifluoroethyl; however, formula (i) and formula (ii) Except for the compounds shown).

[7] A liquid crystal display device, which is characterized by using the liquid crystal composition according to any one of the above [1] to [6].

[8] A liquid crystal display device according to any one of the above [1] to [6], wherein the liquid crystal composition according to any one of the above [1] to [6] is used.

[9] A liquid crystal display device according to any one of the above [1] to [6], wherein the liquid crystal composition according to any one of the above [1] to [6] is used.

[10] A liquid crystal display device according to any one of [1] to [6], wherein the liquid crystal composition according to any one of the above [1] to [6] is used.

[11] A liquid crystal display device according to any one of [1] to [6], wherein the liquid crystal composition according to any one of the above [1] to [6] is used.

[12] A liquid crystal display device according to any one of [1] to [6], wherein the liquid crystal composition according to any one of the above [1] to [6] is used.

[13] A liquid crystal display device using the liquid crystal display device according to any one of the above [7] to [12].

The liquid crystal composition having positive dielectric anisotropy of the present invention is a liquid crystal phase having a wide temperature range, and has a viscosity which is greatly reduced compared with the prior art, and the specific resistance or voltage holding ratio is caused by heat or light. The extent of the change is minimal. Therefore, the liquid crystal composition of the present invention has high practicability (applicability) for a liquid crystal product, and a liquid crystal display element such as an IPS type or an FFS type using the liquid crystal composition can achieve a rapid reaction. In addition, the liquid crystal composition of the present invention can stably exhibit its performance even after passing through the process of the liquid crystal display element, and it is possible to suppress display defects caused by the process, and it is possible to manufacture a liquid crystal display element with high yield, which is very useful.

100‧‧‧1st substrate

102‧‧‧TFT layer

103‧‧‧ pixel electrodes

104‧‧‧passivation film

105‧‧‧1st alignment film

200‧‧‧2nd substrate

201‧‧‧Flating film (covering layer)

202‧‧‧Black matrix

203‧‧‧Color filters

204‧‧‧Transparent electrode

205‧‧‧2nd alignment film

301‧‧‧ sealing material

302‧‧‧protrusions (columnar spacers)

303‧‧‧Liquid layer

304‧‧‧protrusions (columnar spacers)

401‧‧‧ mask pattern

402‧‧‧ resin layer

L‧‧‧Light

Fig. 1 is a cross-sectional view showing a liquid crystal display element of the present invention. A substrate having 100 to 105 is referred to as a "back plate", and a substrate having 200 to 205 is referred to as a "front plate".

Fig. 2 is a view showing an exposure processing step of using a columnar spacer formed on a black matrix as a mask pattern.

[Formation of the Invention]

The liquid crystal composition having a positive dielectric anisotropy according to the first embodiment of the present invention contains a component (A) having a positive dielectric component. The component (A) is a combination of dielectric anisotropy of 2 or more. The composition of things. Further, the dielectric anisotropy of the compound is a value extrapolated from the measured value of the dielectric anisotropy of the composition prepared by adding the liquid crystal composition having a dielectric anisotropy of about 0 at 25 °C.

The "%" in the following composition means "% by mass" unless otherwise specified.

The component (A) contains any one or two or more of the compounds represented by the following formula (i), and one or more of the compounds represented by the following formula (ii).

<Compound represented by the formula (i)>

In the above formula (i), R ^11a represents an alkyl group having 1 to 8 carbon atoms, and one or two or more non-contiguous -CH ₂ - groups of the alkyl group may be independently -CH=CH. -, -C≡C-, -O-, -CO-, -COO- or -OCO-, wherein one or more hydrogen atoms in the alkyl group may be substituted by a fluorine atom or a chlorine atom.

The above R ^{11a is} preferably a linear alkyl group having 1 to 8 carbon atoms, and the alkyl group preferably has 1 to 6 carbon atoms, more preferably 2 to 5 carbon atoms, still more preferably 2 or 3 or 5 carbon atoms, more preferably 2 or 3, especially 3.

In the above formula (i), X ^{11 is} preferably a hydrogen atom or a fluorine atom.

In the above formula (i), X ^{12 is} preferably a fluorine atom or -OCF ₃ .

In the above formula (i), when m ¹¹ is 2, the plural A ^{11 's} may be the same or different from each other.

In the above formula (i), when m ¹¹ is 1, A ^{11 is} preferably a 1,4-phenylene group which may be substituted by a fluorine atom, and when m ¹¹ is 2, at least one of the two existing A ¹¹ is more Preferably, the fluorine atom is substituted by a 1,4-phenylene group, and when m ¹¹ is 2, one of A ¹¹ is a trans-1,4-cyclohexylene group, and the other A ¹¹ is a fluorine atom-substituted one. When the 4-phenyl group is extended, it is preferred that the trans-1,4-cyclohexylene group of the above-mentioned one A ¹¹ is bonded to the above-mentioned cyclohexylene group having an alkyl group, and the two extended cyclohexyl groups are linked.

The kind of the compound which can be combined is not particularly limited, but the plural of the above formula (i) can be combined according to the desired properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Used as a compound. The type of the compound represented by the above formula (i) to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, it is preferably two or more types, and in the case of a plurality of uses, it is preferred to use two kinds of compounds, and it is preferred to use a compound in which each of X ¹² is a fluorine atom and X ¹² is -OCF. ₃ compounds.

The content of the compound represented by the formula (i) is considered to be solubility at low temperature, transition temperature, electron reliability, birefringence, etc., and according to the embodiment, there are preferred upper and lower limits.

The lower limit of the content of the above compound is preferably 1%, preferably 5%, preferably 7%, preferably 9%, based on the total mass of the liquid crystal composition of the present invention. The limit is preferably 25%, preferably 20%, preferably 16%, preferably 12%, preferably 10%, preferably 8%, preferably 7%.

When only one of the above compounds is used, the lower limit of the content of the above compound is preferably 1%, preferably 2%, preferably 5%, preferably 6%, relative to the total mass. The above-mentioned total mass, the upper limit of the content of the aforementioned compound is preferably 25%, preferably 20%, preferably 15%, preferably 12%, preferably 10%, preferably 9%, preferably. It is 7%.

When two or more of the above compounds are used, the lower limit of the total content of the two compounds is preferably 6%, preferably 8%, preferably 10%, based on the total mass, relative to the total mass. The upper limit of the total content of the above two compounds is preferably 25%, preferably 20%, preferably 15%, preferably 12%.

When the solubility of the liquid crystal composition is emphasized, it is preferred to use two kinds of compounds represented by the above formula (i), and when it is desired to increase the content of the compound represented by the formula (i), it is preferred to use two kinds of compounds. The compound.

The content of the compound represented by the above formula (i) is preferably from 1 to 15% by mass, preferably from 1 to 12% by mass, preferably from 1 to 10% by mass based on the total mass. % is preferably from 1 to 9% by mass, and in another embodiment, preferably from 5 to 25% by mass, preferably from 5 to 20% by mass, preferably from 7 to 15% by mass, preferably from 7 to 5% by mass. 13% by mass.

In the above formula (i), m ^{11 is} preferably 1 or 2. When the reaction rate is important, it is preferably 1, and when Tni is important, it is preferably 2.

In the above formula (i), the compound wherein m ¹¹ is 2 is preferably a compound represented by the following formula (X-1). (wherein, X ¹⁰¹ to X ¹⁰³ each independently represent a fluorine atom or a hydrogen atom, and R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkane having 1 to 4 carbon atoms; Oxy).

The compound which can be combined is not particularly limited, but solubility in a low temperature, a transition temperature, an electron reliability, a birefringence, etc. are considered, and the plural represented by the above formula (X-1) is suitably combined for each embodiment. Compound. For example, in one embodiment of the present invention, it is one type. Further, in another embodiment of the present invention, there are two types. In still another embodiment, there are three types. In still another embodiment, there are four types. In still another embodiment, it is five or more types.

The content of the compound represented by the formula (X-1) is in consideration of properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence, and has an upper limit and a lower limit in each embodiment. For example, in one embodiment of the present invention, the content of the compound is 2 to 40% by mass based on the total mass of the liquid crystal composition of the present invention, and in another embodiment, the content of the compound is 3 to 40% by mass. In still another embodiment, the content of the compound is 5 to 40% by mass, and in still another embodiment, the content of the compound is 6 to 40% by mass, and in yet another embodiment, The content of the compound is 7 to 40% by mass, and in still another embodiment, the content of the compound is 8 to 40% by mass, and in still another embodiment, the content of the compound is 9 to 40% by mass. . In still another embodiment, the content of the compound is from 13 to 40% by mass. In still another embodiment, the content of the aforementioned compound is 18 to 40% by mass. In still another embodiment, the content of the compound is from 23 to 40% by mass.

Further, for example, in one embodiment of the present invention, the content of the compound is 2 to 40% by mass based on the total mass, and in another embodiment, the content of the compound is 2 to 30% by mass. In one embodiment, the content of the compound is 2 to 25% by mass, and in still another embodiment, the content of the compound is 2 to 20% by mass. In still another embodiment, the content of the compound is 2 to 15% by mass, in still another embodiment, the content of the compound is 2 to 10% by mass, and in still another embodiment, the content of the compound is 2 to 6% by mass, and further In one embodiment, the content of the compound is from 2 to 4% by mass.

In addition, the compound represented by the formula (X-1) used in the liquid crystal composition of the present invention is preferably a compound represented by the formula (X-1-1). (In the formula, R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but solubility in a low temperature, a transition temperature, an electron reliability, a birefringence, and the like are considered, and each of the embodiments is appropriately combined with the above formula (X-1-1). a compound of plural. For example, in one embodiment of the present invention, it is one type. Further, in another embodiment of the present invention, there are two types. In still another embodiment, there are three types. In still another embodiment, it is four or more types.

The content of the compound represented by the formula (X-1-1) is based on properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence, and has upper and lower limits per embodiment. . For example, in one embodiment of the present invention, the content of the compound is from 3 to 30% by mass based on the total mass of the liquid crystal composition of the present invention, and in another embodiment, the content of the compound is from 4 to 30% by mass. In still another embodiment, the content of the compound is 6 to 30% by mass, and in still another embodiment, the content of the compound is 9 to 30% by mass, and in still another embodiment, The content of the compound is 12 to 30% by mass, and in still another embodiment, the content of the compound is 15 to 30% by mass, and in still another embodiment, the content of the compound is 18 to 30% by mass. . In still another embodiment, the content of the compound is from 21 to 30% by mass.

Further, for example, in one embodiment of the present invention, the content of the compound is from 3 to 30% by mass based on the total mass, and in another embodiment, the content of the compound is from 3 to 20% by mass. In one embodiment, the content of the compound is 3 to 13% by mass, and in still another embodiment, the content of the compound is 3 to 10% by mass. In still another embodiment, the content of the compound is 3 to 7 mass%.

Further, the compound represented by the formula (X-1-1) used in the liquid crystal composition of the present invention is specifically preferably a compound represented by the formula (36.1) to the formula (36.4), and preferably contains A compound represented by the formula (36.1) and/or the formula (36.2).

In the above formula (i), the compound wherein m ¹¹ is 2 is preferably a compound represented by the following formula (X-1-2). (In the formula, R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The content of the compound represented by the formula (X-1-2) is preferably 1% by mass or more, more preferably 2% by mass or more, and particularly preferably 6% by mass or more based on the total mass of the liquid crystal composition of the present invention. . In addition, the maximum ratio is preferably 15% by mass or less, more preferably 13% by mass or less, even more preferably 10% by mass or less, and particularly preferably 9% by mass or less, in view of solubility at low temperature, transition temperature, and electronic reliability. .

More specifically, the content is 1 to 10% by mass, 2 to 8% by mass, 2 to 7% by mass, 2 to 5% by mass, 4 to 8% by mass, and 5 to 8% by mass. Implementation form.

The compound represented by the above formula (X-1-2) is specifically preferably a compound represented by the formula (37.1) to the formula (37.4), and preferably a compound represented by the formula (37.2).

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (37.2) is preferably a solubility at a low temperature, a transition temperature, an electron reliability, etc., and is preferably based on the total mass of the liquid crystal composition of the present invention. It is 1% by mass or more and 20% by mass or less, more preferably 2% by mass or more and 15% by mass or less, and particularly preferably 2% by mass or more and 10% by mass or less, and particularly preferably 2% by mass or more and 8% by mass or less.

In the above formula (i), the compound wherein m ¹¹ is 2 is preferably a compound represented by the following formula (X-1-3). (In the formula, R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but in view of solubility at low temperature, transition temperature, electron reliability, birefringence and the like, it is preferred to combine the above formula (X-1-3) of one type or two types or more. ) the compound shown.

The content of the compound represented by the formula (X-1-3) is preferably 1% by mass or more, more preferably 2% by mass or more, and particularly preferably 3% by mass or more based on the total mass of the liquid crystal composition of the present invention. . Further, the maximum ratio is preferably 15% by mass or less, more preferably 10% by mass or less, even more preferably 8% by mass or less, and particularly preferably 7% by mass or less, in view of solubility at low temperature, transition temperature, electronic reliability, and the like. .

More specifically, the content is 1 to 10% by mass, 3 to 8% by mass, 2 to 6% by mass, 2 to 5% by mass, 2 to 4% by mass, and 3 to 7% by mass, 4 to 7 mass% and 5 to 7 mass% of the embodiment.

The compound represented by the above formula (X-1-3) is specifically preferably a compound represented by the formula (38.1) to the formula (38.4), and preferably a compound represented by the formula (38.2).

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (38.2) is preferably 1% by mass or more and 15% by mass or less, more preferably 2% by mass based on the total mass of the liquid crystal composition of the present invention. 10% by mass or less is particularly preferably 3% by mass or more and 8% by mass or less, and particularly preferably 4% by mass or more and 6% by mass or less.

In the above formula (i), the compound wherein m ¹¹ is 2 is preferably a compound represented by the following formula (X-2). (wherein, X ¹⁰² to X ¹⁰³ each independently represent a fluorine atom or a hydrogen atom, Y ¹⁰ represents a fluorine atom, a chlorine atom, -OCF ₃ , and R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, and 2 to 2 carbon atoms; 5 alkenyl or alkoxy having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but it is preferably one of the plural compounds represented by the above formula (X-2) in consideration of solubility at low temperature, transition temperature, electron reliability, birefringence and the like. Kind to more than 2 types of combinations.

In the above formula (i), the compound wherein m ¹¹ is 2 is preferably a compound represented by the following formula (X-2-1). (In the formula, R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but it is preferably one type to two types or more, more preferably one type to three types, in consideration of solubility at low temperature, transition temperature, electron reliability, birefringence and the like. The compound represented by the above formula (X-2-1).

The content of the compound represented by the formula (X-2-1) is considered to be solubility at a low temperature, a transition temperature, an electron reliability, and the like, and is preferably 3% by mass based on the total mass of the liquid crystal composition of the present invention. The above is 15% by mass or less, more preferably 4% by mass or more and 10% by mass or less, and particularly preferably 4% by mass or more and 7% by mass or less.

In addition, the compound represented by the formula (X-2-1) used in the liquid crystal composition of the present invention is specifically preferably a compound represented by the formula (39.1) to the formula (39.4), and preferably contains a compound. A compound represented by the formula (39.2).

In the liquid crystal composition of the present invention, the formula represented by the formula (39.2) The content of the compound is more preferably 2% by mass or more and 15% by mass or less, more preferably 3% by mass or more and 15% by mass or less, and even more preferably 3% by mass or more and 10% by mass based on the total mass of the liquid crystal composition of the present invention. % or less is more preferably 4% by mass or more and 8% by mass or less, and particularly preferably 4% by mass or more and 7% by mass or less.

In the range of particularly good, the content may be 4 to 6% by mass, may be 4 to 5% by mass, may be 5 to 7% by mass, and may be 6 to 7% by mass.

In the above formula (i), the compound wherein m ¹¹ is 2 is preferably a compound represented by the following formula (X-2-2). (In the formula, R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but in view of solubility at low temperature, transition temperature, electron reliability, birefringence and the like, it is preferably a compound of the plural compound represented by the above formula (X-2-2). One type to two or more types are combined. The content of the compound represented by the formula (X-2-2) is considered to be solubility at a low temperature, a transition temperature, an electron reliability, and the like, and is preferably 3% by mass based on the total mass of the liquid crystal composition of the present invention. The amount is 20% by mass or less, more preferably 6% by mass or more and 16% by mass or less, and particularly preferably 9% by mass or more and 12% by mass or less, and particularly preferably 9% by mass or more and 10% by mass or less.

Further, the compound represented by the formula (X-2-2) used in the liquid crystal composition of the present invention is specifically preferably a compound represented by the formula (40.1) to the formula (40.4), and preferably contains a compound. A compound represented by the formula (40.2).

In the above formula (i), the compound wherein m ¹¹ is 1, is preferably a compound represented by the following formula (XIV-2-2). (In the formula, R ¹⁴⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The content of the compound represented by the formula (XIV-2-2) is considered to be solubility at a low temperature, a transition temperature, an electron reliability, etc., and is preferably 1% by mass based on the total mass of the liquid crystal composition of the present invention. The amount is 20% by mass or less, more preferably 1% by mass or more and 15% by mass or less, and particularly preferably 2% by mass or more and 10% by mass or less, and particularly preferably 3% by mass or more and 7% by mass or less.

Further, the compound represented by the formula (XIV-2-2) is specifically preferably a compound represented by the formula (54.1) to the formula (54.4), and preferably contains the formula (54.2) and/or the formula (54.4). ) the compound shown.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (54.2) is preferably 1% by mass or more and 35% by mass or less, more preferably 1% by mass based on the total mass of the liquid crystal composition of the present invention. The amount is preferably 25% by mass or less, more preferably 1% by mass or more and 20% by mass or less, more preferably 1% by mass or more and 15% by mass or less, still more preferably 1% by mass or more and 10% by mass or less, and particularly preferably 2% by mass or more. The mass% or less is particularly preferably 3% by mass or more and 7% by mass or less.

The content may be from 3 to 5% by mass, and may also be from 5 to 7% by mass in the range of particularly preferred.

When two kinds of compounds represented by the formula (i) are used, a combination of the compounds represented by the formula (37.2) and the formula (39.2) and a combination of the compounds represented by the formula (38.2) and the formula (39.2) are preferred. .

In the above formula (i), the compound wherein m ¹¹ is 1, is preferably a compound represented by the following formula (XIV-2-3). (In the formula, R ¹⁴⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The content of the compound represented by the formula (XIV-2-3) is considered to be solubility at a low temperature, a transition temperature, an electron reliability, and the like, and is preferably 5% by mass based on the total mass of the liquid crystal composition of the present invention. The amount is 30% by mass or less, more preferably 9% by mass or more and 27% by mass or less, and particularly preferably 12% by mass or more and 24% by mass or less, and particularly preferably 12% by mass or more and 20% by mass or less.

Further, the compound represented by the formula (XIV-2-3) is specifically preferably a compound represented by the formula (55.1) to the formula (55.4), and preferably contains the formula (55.2) and/or the formula (55.4). ) the compound shown.

In the above formula (i), the compound wherein m ¹¹ is 1, is preferably a compound represented by the following formula (XIV-2-4). (In the formula, R ¹⁴⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The type of the compound that can be combined is not limited, but solubility in a low temperature, transition temperature, electron reliability, birefringence, and the like can be considered, and the combination of the above formula (XIV-2-4) is suitably combined for each embodiment. a compound of plural. For example, in one embodiment of the present invention, it is one type. Furthermore, in another embodiment of the present invention, there are two types. Alternatively, in still another embodiment of the present invention, it is three or more types.

The content of the compound represented by the formula (XIV-2-4) is based on properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence, and has an upper limit and a lower limit in each embodiment. .

For example, in one embodiment of the present invention, the content of the compound is 2 to 35% by mass based on the total mass of the liquid crystal composition of the present invention, and in another embodiment, the content of the compound is 5 to 35 mass. In still another embodiment, the content of the compound is 8 to 35% by mass, and in still another embodiment, the content of the compound is 9 to 35% by mass, and in still another embodiment, The content of the compound is 10 to 35 mass%, and in still another embodiment, the content of the compound is 18 to 35 mass%, and in still another embodiment, the content of the compound is 21 to 35 mass%. . In still another embodiment, the content of the compound is from 22 to 35% by mass. In still another embodiment, the content of the compound is from 24 to 35% by mass.

Further, for example, in one embodiment of the present invention, the content of the compound is 2 to 35% by mass based on the total mass, and in another embodiment, the content of the compound is 2 to 30% by mass. In one embodiment, the content of the compound is 2 to 25% by mass, In still another embodiment, the content of the compound is 2 to 20% by mass, and in still another embodiment, the content of the compound is 2 to 15% by mass. In still another embodiment, the compound The content is 2 to 10% by mass.

When the liquid crystal composition of the present invention is used for a liquid crystal display element having a small driving voltage, the content of the compound represented by the formula (XIV-2-4) is preferably slightly more. Further, in the case of a liquid crystal composition used for a liquid crystal display element having a high reaction rate, the content of the compound represented by the formula (XIV-2-4) is preferably slightly less.

Further, the compound represented by the formula (XIV-2-4) is specifically preferably a compound represented by the formula (56.1) to the formula (56.4), and preferably contains the formula (56.1), the formula (56.2) and / or a compound of the formula (56.4).

In the above formula (i), the compound wherein m ¹¹ is 1, is preferably a compound represented by the following formula (XIV-2-5). (In the formula, R ¹⁴⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The content of the compound represented by the formula (XIV-2-5) is considered to be solubility at a low temperature, a transition temperature, an electron reliability, etc., and is preferably 5% by mass based on the total mass of the liquid crystal composition of the present invention. The above is 25% by mass or less, more preferably 10% by mass or more and 22% by mass or less, and particularly preferably 13% by mass or more and 18% by mass or less, and particularly preferably 13% by mass or more and 15% by mass or less.

Further, the compound represented by the formula (XIV-2-5) is specifically a compound represented by the formula (57.1) to the formula (57.4). Among them, preferred is a compound represented by the formula (57.1).

In the above formula (i), the compound wherein m ¹¹ is 1, is preferably a compound represented by the following formula (XIV-2-6). (In the formula, R ¹⁴⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The content of the compound represented by the formula (XIV-2-6) is considered to be solubility at a low temperature, a transition temperature, an electron reliability, and the like, and is preferably 5% by mass based on the total mass of the liquid crystal composition of the present invention. The amount is preferably 25% by mass or less, more preferably 10% by mass or more and 22% by mass or less, still more preferably 15% by mass or more and 20% by mass or less, and particularly preferably 15% by mass or more and 17% by mass or less.

Further, the compound represented by the formula (XIV-2-6) is specifically preferably a compound represented by the formula (58.1) to the formula (58.4), and preferably a compound represented by the formula (58.2).

<Compound represented by the formula (ii)>

In the above formula (ii), R ^{21a is} preferably a linear alkyl group having 1 to 8 carbon atoms, and the number of carbon atoms is preferably from 1 to 6, more preferably from 2 to 5, still more preferably from 2 to 3.

In the above formula (ii), m ²¹ represents 0 or 1, X ²¹ , X ²² , X ²³ and X ²⁴ each independently represent a hydrogen atom, a fluorine atom or a chlorine atom, and X ²⁵ represents a hydrogen atom, a fluorine atom or a chlorine atom. , cyano, -CF ₃ or -OCF ₃ .

m ^{21 is} preferably 1.

When m ²¹ is 1, preferably X ²¹ and X is at least one hydrogen atom is ^22, more preferably both X ²¹ and X ²² is a hydrogen atom.

X ²³ , X ²⁴ and X ²⁵ are each independently preferably a fluorine atom, and preferably at least two of X ²³ , X ²⁴ and X ²⁵ are fluorine atoms, more preferably all of X ²³ , X ²⁴ and X ²⁵ It is a fluorine atom.

Further, it is preferred that at least two of X ²¹ to X ²⁴ are fluorine atoms.

The compound represented by the above formula (ii) is preferably a compound represented by the formula (X-6). (In the formula, R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but it is preferably one or two or more types in combination with the above formula (X-6) in consideration of solubility at low temperature, transition temperature, electron reliability, and birefringence. The compound shown.

The content of the compound represented by the formula (ii) is based on the characteristics of solubility at low temperature, transition temperature, electron reliability, and birefringence. There are upper and lower limits for each embodiment.

When only one of the foregoing compounds is used, the lower limit of the content of the above compound is preferably 1%, more preferably 2%, and particularly preferably 3%, relative to the total mass, and the aforementioned The upper limit of the content of the compound is preferably 15%, more preferably 12%, still more preferably 10%, particularly preferably 8%, most preferably 7%.

When two of the above compounds are used, the lower limit of the total content of the above two compounds is preferably 4%, more preferably 5%, and particularly preferably 6%, relative to the total mass, with respect to the aforementioned total mass. The upper limit of the total content of the above two compounds is preferably 25%, more preferably 20%, particularly preferably 18%, and particularly preferably 16%.

When the solubility of the liquid crystal composition is emphasized, it is preferred to use two kinds of the compounds represented by the above formula (ii), and when it is desired to increase the content of the compound represented by the formula (ii), it is preferably used. Two kinds of this compound.

For example, in one embodiment of the present invention, the content of the compound is from 3 to 30% by mass based on the total mass of the liquid crystal composition of the present invention, and is from 3 to 25% by mass in another embodiment. In one embodiment, it is 3 to 10% by mass, and in still another embodiment, it is 3 to 7% by mass, and in still another embodiment, it is 5 to 10% by mass. In still another embodiment, 6 to 16% by mass, and in still another embodiment, 14 to 20% by mass.

Further, for example, in one embodiment of the present invention, the content of the compound is from 1 to 30% by mass based on the total mass of the liquid crystal composition of the present invention, and is from 1 to 20% by mass in another embodiment. In another embodiment, it is 1 to 13% by mass, and in still another embodiment, 1 to 10% by mass, and in still another embodiment, it is 1 to 7% by mass, and in still another embodiment, it is 1 to 3% by mass.

In addition, the compound represented by the formula (X-6) used in the liquid crystal composition of the present invention is specifically preferably a compound represented by the formula (44.1) to the formula (44.4). Among these, it is preferred to contain a compound represented by the formula (44.1) and/or the formula (44.2).

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (44.1) is considered to be solubility at a low temperature, a transition temperature, an electron reliability, etc., and is preferably based on the total mass of the liquid crystal composition of the present invention. It is 1% by mass or more and 25% by mass or less, more preferably 3% by mass or more and 20% by mass or less, and particularly preferably 3% by mass or more and 15% by mass or less, particularly preferably 3% by mass or more and 10% by mass or less, and most preferably 3 The mass% or more is 8% by mass or less.

In an optimum range, the content may be 3% by mass or more and 6% by mass or less, may be 3% by mass or more and 4% by mass or less, may be 4% by mass or more and 8% by mass or less, and may be 6% by mass or more. Below mass%, can be 7 The mass% or more is 8% by mass or less.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (44.2) is preferably a solubility at a low temperature, a transition temperature, an electron reliability, etc., and is preferably based on the total mass of the liquid crystal composition of the present invention. It is 1% by mass or more and 25% by mass or less, more preferably 3% by mass or more and 20% by mass or less, and particularly preferably 3% by mass or more and 15% by mass or less, particularly preferably 3% by mass or more and 10% by mass or less, and most preferably 3 The mass% or more is 8% by mass or less.

In an optimum range, the content may be 3% by mass or more and 6% by mass or less, may be 3% by mass or more and 4% by mass or less, may be 4% by mass or more and 8% by mass or less, and may be 6% by mass or more. The mass% or less may be 7 mass% or more and 8 mass% or less.

In the liquid crystal composition of the present invention, the total content of the compound represented by the formula (44.1) and the compound represented by the formula (44.2) is considered in consideration of solubility at low temperature, transition temperature, electron reliability, and the like, with respect to the present invention. The total mass of the liquid crystal composition is preferably 5% by mass or more and 45% by mass or less, more preferably 5% by mass or more and 25% by mass or less, still more preferably 6% by mass or more and 20% by mass or less, and particularly preferably 6% by mass or less. The above is 16% by mass or less.

In the above-mentioned range, the content is, for example, 6 mass% or more and 15 mass% or less, 6 mass% or more and 12 mass% or less, 6 mass% or more and 10 mass% or less, and 6 mass% or more and 8 mass% or less. 8% by mass or more and 16% by mass or less, 10% by mass or more and 16% by mass or less, 12% by mass or more and 16% by mass or less, and 15% by mass or more and 16% by mass or less.

The compound represented by the formula (i) and the compound represented by the formula (ii) are preferably used in total of 2 to 4 kinds, more preferably 3 or 4 types.

With respect to the total mass of the liquid crystal composition of the present invention, the formula (i) is shown The lower limit of the total content of the compound and the compound represented by the formula (ii) is preferably 4%, more preferably 6%, still more preferably 8%, particularly preferably 10%. The upper limit of the total content is preferably 40%, more preferably 35%, particularly preferably 30%, particularly preferably 27%, and most preferably 20%, based on the total mass.

When two kinds of the compound represented by the above formula (i) and the compound represented by the above formula (ii) are used in combination, the lower limit of the total content of the two compounds is higher than the total mass. Preferably, it is 6%, preferably 8%, more preferably 10%, and particularly preferably 12%. The upper limit of the total content of the above two compounds is preferably 20%, more preferably 18%, still more preferably 16%, particularly preferably 14%, based on the total mass.

When one or two kinds of the compounds represented by the above formula (i) and two or more of the compounds represented by the above formula (ii) are used in combination, the above three types are used in combination with the total mass. The lower limit of the total content of the compound is preferably 5%, more preferably 8%, and particularly preferably 10%. The upper limit of the total content of the above three compounds is preferably 30%, more preferably 24%, particularly preferably 21%, particularly preferably 18%, based on the total mass.

When a total of four types of the compound represented by the above formula (i) and one or three kinds of the compound represented by the above formula (ii) are used, the total content of the above four compounds is based on the total mass. The lower limit is preferably 15%, more preferably 17%, still more preferably 19%, particularly preferably 20%, and most preferably 24%. The upper limit of the total content of the above four compounds is preferably 40%, more preferably 35%, particularly preferably 30%, particularly preferably 27%, based on the total mass.

When the solubility of the liquid crystal composition is emphasized, it is preferred to use two or four of the above totals.

A preferred combination is preferably a compound represented by formula (37.2) and formula (44.2). a combination of compounds represented by formula (37.2), formula (44.1), and formula (44.2), a combination of compounds represented by formula (37.2), formula (39.2), formula (44.1), and formula (44.2), and A combination of compounds represented by formula (38.2), formula (39.2), formula (44.1), and formula (44.2).

The liquid crystal composition of the first embodiment of the present invention may contain any one or two or more kinds of the compounds represented by the following formula (L). (wherein R ^L1 and R ^L2 each independently represent an alkyl group having 1 to 8 carbon atoms, and one of the alkyl groups or two or more non-adjacent-CH ₂ - groups may independently be -CH =CH-, -C≡C-, -O-, -CO-, -COO- or -OCO-substitution, OL means 0, 1, 2 or 3, B ^L1 , B ^L2 and B ^L3 are each independently represented Free (a) 1,4-cyclohexylene (one -CH ₂ - or two or more -CH ₂ - which are not adjacent in this group may be substituted into -O-) and (b) 1,4 a group in a group consisting of a phenyl group (one -CH= or a non-contiguous two or more -CH= can be substituted into -N=), the above group (a), One or two or more hydrogen atoms in the group (b) may be independently substituted by a cyano group, a fluorine atom or a chlorine atom, and L ^L1 and L ^L2 each independently represent a single bond, -CH ₂ CH ₂ -, - (CH ₂ ) ₄ -, -OCH ₂ -, -CH ₂ O-, -COO-, -OCO-, -OCF ₂ -, -CF ₂ O-, -CH=NN=CH-, -CH=CH- , -CF=CF- or -C≡C-, when OL is 2 or 3 and L ^L2 is plural, they may be the same or different. When OL is 2 or 3 and B ^L3 is plural, Etc. can be the same or different).

The type of the compound which can be combined is not particularly limited, but may be appropriately combined with the above formula (L) in accordance with the desired properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Used as a compound. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types. Further, in another embodiment of the present invention, there are three types. Furthermore, in another embodiment of the present invention, there are four types. Furthermore, in another embodiment of the present invention, there are five types. Furthermore, in another embodiment of the present invention, there are six types. Furthermore, in another embodiment of the present invention, there are seven types. Furthermore, in another embodiment of the present invention, there are eight types. Furthermore, in another embodiment of the present invention, there are nine types. Furthermore, in another embodiment of the present invention, it is 10 or more types.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (L) must be in accordance with solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, dripping marks, branding, and intercalation. The required performance such as electrical anisotropy is suitably adjusted.

The content of the above compound is, for example, 1 to 95% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Alternatively, in another embodiment of the present invention, the content is 10 to 95% by mass. Furthermore, in another embodiment of the present invention, the content is 20 to 95% by mass. Furthermore, in another embodiment of the present invention, the content is 30 to 95% by mass. Furthermore, another implementation of the present invention In the form, the content is 40 to 95% by mass. Furthermore, in another embodiment of the present invention, the content is 50 to 95% by mass. Furthermore, in another embodiment of the present invention, the content is 55 to 95% by mass. Furthermore, in another embodiment of the present invention, the content is 60 to 95% by mass. Furthermore, in another embodiment of the present invention, the content is 65 to 95% by mass. Furthermore, in another embodiment of the present invention, the content is 70 to 95% by mass. Furthermore, in another embodiment of the present invention, the content is 75 to 95% by mass. Furthermore, in another embodiment of the present invention, the content is 80 to 95% by mass.

In addition, the content of the above compound is, for example, 1 to 95% in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content is 1 to 85%. Furthermore, in another embodiment of the present invention, the content is 1 to 75%. Furthermore, in another embodiment of the present invention, the content is 1 to 65%. Furthermore, in another embodiment of the present invention, the content is 1 to 55%. Furthermore, in another embodiment of the present invention, the content is 1 to 45%. Furthermore, in another embodiment of the present invention, the content is 1 to 35%. Furthermore, in another embodiment of the present invention, the content is 1 to 25%.

When the liquid crystal composition of the present invention has a low viscosity and requires a liquid crystal composition having a high reaction rate, it is preferred that the lower limit value is higher and the upper limit value is higher. In addition, when the liquid crystal composition of the liquid crystal composition of the present invention is high and a liquid crystal composition having good temperature stability is required, it is preferable that the lower limit value is higher and the upper limit value is higher. Further, in order to increase the dielectric anisotropy in order to maintain a low driving voltage, it is preferable that the above lower limit value is low. And the upper limit is lower.

R ^L1 and R ^L2 are preferably a linear alkyl group having 1 to 5 carbon atoms and a linear carbon number of 1 to 4 when the ring to which the ring is bonded is a phenyl group (aromatic). (or more) alkoxy group and alkenyl group having 4 to 5 carbon atoms, wherein the ring to which the bond is bonded is cyclohexane, megbrane and In the case of a saturated ring structure such as an alkane, a linear alkyl group having 1 to 5 carbon atoms, a linear alkoxy group having 1 to 4 (or more) carbon atoms, and a linear carbon are preferable. An alkenyl group having 2 to 5 atoms.

When the chemical stability of the liquid crystal composition is required, the compound represented by the formula (L) preferably has no chlorine atom in its molecule.

The compound represented by the formula (L) is preferably, for example, a compound selected from the group of compounds represented by the formula (I), R ¹¹ -A ¹¹ -A ¹² -R ¹² (I) (wherein R ¹¹ and R ¹² each independently represents an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms, and A ¹¹ and A ¹² each independently represent 1,4- Cyclohexyl, 1,4-phenylene, 2-fluoro-1,4-phenylene or 3-fluoro-1,4-phenylene).

The kind of the compound which can be combined is not particularly limited, but may be a combination of the above-described general formula (I) in accordance with the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Used as a compound. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types. Further, in another embodiment of the present invention, there are three types. Furthermore, in another embodiment of the present invention, there are four types. again In another embodiment of the present invention, it is five or more types. Furthermore, in another embodiment of the present invention, it is six or more types.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (I) must be in accordance with solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, dripping marks, branding, and intercalation. The required performance such as electrical anisotropy is suitably adjusted.

The content of the above compound is, for example, 3 to 75% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Alternatively, in another embodiment of the present invention, the content is 15 to 75% by mass. Furthermore, in another embodiment of the present invention, the content is 18 to 75% by mass. Furthermore, in another embodiment of the present invention, the content is 20 to 75% by mass. Furthermore, in another embodiment of the present invention, the content is 29 to 75% by mass. Furthermore, in another embodiment of the present invention, the content is 35 to 75% by mass. Furthermore, in another embodiment of the present invention, the content is 42 to 75% by mass. Furthermore, in another embodiment of the present invention, the content is 47 to 75% by mass. Furthermore, in another embodiment of the present invention, the content is 53 to 75% by mass. Furthermore, in another embodiment of the present invention, the content is 56 to 75% by mass. Furthermore, in another embodiment of the present invention, the content is 60 to 75% by mass. Furthermore, in another embodiment of the present invention, the content is 65 to 75% by mass.

In addition, the content is, for example, 3 to 75% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Further, in another embodiment of the present invention, the content is 3 to 65% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 55 quality%. Furthermore, in another embodiment of the present invention, the content is 3 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 45% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is from 3 to 35% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 30% by mass.

When the liquid crystal composition of the present invention has a low viscosity and requires a liquid crystal composition having a high reaction rate, it is preferred that the lower limit value is higher and the upper limit value is higher. In addition, when the liquid crystal composition of the liquid crystal composition of the present invention is high and a liquid crystal composition having good temperature stability is required, it is preferable that the above lower limit value is moderate and the upper limit is moderate. Further, in order to increase the dielectric anisotropy in order to maintain a low driving voltage, it is preferable that the above lower limit value is lower and the upper limit value is lower.

R ^M1 is preferably a linear alkyl group having 1 to 5 carbon atoms and a linear alkoxy group having 1 to 4 carbon atoms when the ring to which the ring is bonded is a phenyl group (aromatic). And an alkenyl group having 4 to 5 carbon atoms, wherein the ring to which the bond is bonded is cyclohexane, meme, and In the case of a saturated ring structure such as an alkane, a linear alkyl group having 1 to 5 carbon atoms, a linear alkoxy group having 1 to 4 carbon atoms, and a linear carbon number of 2 to 5 are preferable. Alkenyl.

Further, the compound represented by the formula (I) is preferably a compound selected from the group of compounds represented by the formula (I-1). (wherein R ¹¹ and R ¹² each independently represent an alkyl group having 1 to 5 carbon atoms, an alkoxy group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms).

The kind of the compound which can be combined is not particularly limited, but may be suitably combined with the properties shown in the above formula (I-1) according to the properties required for solubility at low temperature, transition temperature, electron reliability, birefringence and the like. A plurality of compounds are used. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types. Further, in another embodiment of the present invention, it is three or more types. Furthermore, in another embodiment of the present invention, there are four types. Furthermore, in another embodiment of the present invention, it is five or more types.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (I-1) must be in accordance with solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, dripping marks, and imprinting. The required performance such as dielectric anisotropy is appropriately adjusted.

The content of the above compound is, for example, in one embodiment of the present invention, the content of the compound is from 3 to 70% by mass based on the total mass of the liquid crystal composition of the present invention. Alternatively, in another embodiment of the present invention, the content is 15 to 70% by mass. Furthermore, in another embodiment of the present invention, the content is 18 to 70% by mass. Furthermore, in another embodiment of the present invention, the content is 25 to 70% by mass. Furthermore, in another embodiment of the present invention, the content is 29 to 70% by mass. Furthermore, in another embodiment of the present invention, the content is 31 to 70% by mass. Furthermore, in another embodiment of the present invention, the content is 35 to 70% by mass. Furthermore, in another embodiment of the present invention, the content is 43 to 70% by mass. Furthermore, in another embodiment of the present invention, the content is 47 to 70% by mass. Furthermore, in another embodiment of the present invention, the content is 50 to 70% by mass. Furthermore, in another embodiment of the present invention In the above, the content is 53 to 70% by mass. Furthermore, in another embodiment of the present invention, the content is 56 to 70% by mass.

The content of the compound is, for example, in one embodiment of the present invention, the content of the compound is from 3 to 70% by mass based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content is from 3 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 45% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is from 3 to 35% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 30% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 26% by mass.

When the liquid crystal composition of the present invention has a low viscosity and requires a liquid crystal composition having a high reaction rate, it is preferred that the lower limit value is higher and the upper limit value is higher. In addition, when the liquid crystal composition of the liquid crystal composition of the present invention is high and a liquid crystal composition having good temperature stability is required, it is preferable that the above lower limit value is moderate and the upper limit is moderate. Further, in order to increase the dielectric anisotropy in order to maintain a low driving voltage, it is preferable that the above lower limit value is lower and the upper limit value is lower.

Further, the compound represented by the formula (I-1) is preferably a compound selected from the group of compounds represented by the formula (I-1-1). (wherein R ¹² each independently represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 5 carbon atoms).

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (I-1-1) must be in accordance with solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, and dripping traces. The performance required for branding, dielectric anisotropy, etc., is suitably adjusted.

The content of the above compound is, for example, 2 to 60% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Alternatively, in another embodiment of the present invention, the content is 4 to 60% by mass. Further, in another embodiment of the present invention, the content is 7 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 11 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 13 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 15 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 17 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 20 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 25 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 30 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 32 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 35 to 60% by mass.

The content of the above compound is, for example, 2 to 60% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Further, in another embodiment of the present invention, the content is 2 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 2 to 40% by mass. Furthermore, in another embodiment of the present invention, the front The content is 2 to 35% by mass. Furthermore, in another embodiment of the present invention, the content is 2 to 30% by mass. Furthermore, in another embodiment of the present invention, the content is 2 to 25% by mass. Furthermore, in another embodiment of the present invention, the content is 2 to 20% by mass. Furthermore, in another embodiment of the present invention, the content is 2 to 15% by mass.

Further, the compound represented by the formula (I-1-1) is preferably a compound selected from the group of compounds represented by the formula (1.1) to the formula (1.3), preferably a formula (1.2) or a formula (1.3). The compound shown is particularly preferably a compound represented by the formula (1.3).

When the compound represented by the formula (1.2) or the formula (1.3) is used singly, the compound of the formula (1.2) is contained in an amount effective to improve the reaction rate, and the content of the compound represented by the formula (1.3) is The range shown below is preferably a liquid crystal composition having a high reaction speed and high electronic and optical reliability.

The compound represented by the formula (1.3) is preferably 5% by mass or more and 35% by mass or less, more preferably 5% by mass or more and 30% by mass or less, more preferably 5% by mass or more, based on the total mass of the liquid crystal composition of the present invention. The content is preferably 5% by mass or more and 25% by mass or less, more preferably 5% by mass or more and 20% by mass or less, and most preferably 5% by mass or more and 17% by mass or less.

Among the contents of the optimum range, for example, 5% by mass or more and 15% by mass or less, 5% by mass or more and 12% by mass or less, and 5% by mass or more and 10% are exemplified. 5% by mass or less, 5% by mass or more and 8% by mass or less, 5% by mass or more and 7% by mass or less, 7% by mass or more and 17% by mass or less, 8% by mass or more and 17% by mass or less, 10% by mass or more and 17% by mass or less, and 12% by mass or more and 17% by mass or less, 12 The content is 17% by mass or less, 14% by mass or more and 17% by mass or less, and 15% by mass or more and 17% by mass or less by mass or more.

Further, the compound represented by the formula (I-1) is preferably a compound selected from the group of compounds represented by the formula (I-1-2). (wherein R ¹² each independently represents an alkyl group having 1 to 5 carbon atoms, an alkoxy group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms).

The kind of the compound which can be combined is not particularly limited, but the above formula (I-1-2) can be suitably combined according to the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. The compound of the plural is used. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types. Further, in another embodiment of the present invention, there are three types.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (I-1-2) must be in accordance with solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, and dripping traces. The performance required for branding, dielectric anisotropy, etc., is suitably adjusted.

The content of the above compound is, for example, 7 to 60% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Or in another embodiment of the present invention, the aforementioned content It is 15 to 60% by mass. Further, in another embodiment of the present invention, the content is from 18 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 21 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 24 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 27 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 30 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 34 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 37 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 41 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 47 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 50 to 60% by mass.

In addition, the content of the compound is, for example, 7 to 60% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content is 7 to 55% by mass. Furthermore, in another embodiment of the present invention, the content is 7 to 45% by mass. Furthermore, in another embodiment of the present invention, the content is 7 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 7 to 35% by mass. Furthermore, in another embodiment of the present invention, the content is 7 to 30% by mass. Furthermore, in another embodiment of the present invention, the content is 7 to 25% by mass. Furthermore, in another embodiment of the present invention, the content is 7 to 20% by mass.

Further, the compound represented by the formula (I-1-2) is preferably a compound selected from the group consisting of compounds represented by the formulae (2.1) to (2.4), preferably A compound represented by the formula (2.2) to the formula (2.4). In particular, the compound represented by the formula (2.2) is preferred because it particularly improves the reaction rate of the liquid crystal composition of the present invention. Further, when the Tni which is required to be high is more preferable than the reaction rate, it is preferred to use a compound represented by the formula (2.3) or the formula (2.4). The content of the compound represented by the formula (2.3) and the formula (2.4) is preferably 30% or more in order to improve the solubility at a low temperature.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (2.2) is preferably 5% by mass or more and 55% by mass or less based on the total mass of the liquid crystal composition of the present invention. More preferable examples of the content include 10% by mass or more and 40% by mass or less, 14% by mass or more and 40% by mass or less, 17% by mass or more and 40% by mass or less, 19% by mass or more, 40% by mass or less, and 22% by mass. 40% by mass or less, 25% by mass or more and 40% by mass or less, 27% by mass or more and 40% by mass or less, 30% by mass or more and 40% by mass or less, 33% by mass or more and 40% by mass or less, and 36% by mass or more and 40% by mass or less the following.

Among these ranges, it is particularly preferably 25% by mass or more and 40% by mass or less. In the above-mentioned range, the content is, for example, 25% by mass or more and 35% by mass or less, 25% by mass or more and 30% by mass or less, 30% by mass or more and 40% by mass or less, and 35% by mass or more and 40% by mass or less. content.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (2.3) is preferably 5% by mass or more and 55% by mass or less, more preferably 5% by mass based on the total mass of the liquid crystal composition of the present invention. The above 45 mass% or less, more preferably 5% by mass or more and 35 mass% or less, and particularly preferably 5% by mass or more and 25% by mass or less, particularly preferably 5% by mass or more and 20% by mass or less, particularly preferably 8% by mass or more and 18%. The mass% or less is preferably 11% by mass or more and 15% by mass or less. In an optimum range, for example, the content is 11% by mass or more and 13% by mass or less, and 14% by mass or more and 15% by mass or less.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (2.4) is preferably 1% by mass or more and 55% by mass or less, more preferably 3% by mass based on the total mass of the liquid crystal composition of the present invention. 45质量% or less, more preferably 3% by mass or more and 35% by mass or less, more preferably 3% by mass or more and 25% by mass or less, particularly preferably 5% by mass or more and 15% by mass or less, and most preferably 8% by mass or more. Below mass%.

The liquid crystal composition of the present invention may further contain a compound represented by the formula (2.5) having a structure similar to the compound represented by the formula (I-1-2).

It is preferred to adjust the content of the compound represented by the formula (2.5) in accordance with the properties required for solubility at low temperature, transition temperature, electron reliability, birefringence, etc., with respect to the total mass of the liquid crystal composition of the present invention. In particular, it is preferably contained in an amount of 11% by mass or more, more preferably 15% by mass, still more preferably 23% by mass, still more preferably 26% by mass. The above is particularly preferably contained in an amount of 28% by mass or more.

Further, the compound represented by the formula (I) is preferably a compound selected from the group of compounds represented by the formula (I-2). (wherein R ¹³ and R ¹⁴ each independently represent an alkyl group having 1 to 5 carbon atoms).

The kind of the compound which can be combined is not particularly limited, but the plural number represented by the above formula (I-2) can be combined in accordance with the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Compound. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types. Further, in another embodiment of the present invention, there are three types.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (I-2) must be in accordance with solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, dripping marks, and imprinting. The required performance such as dielectric anisotropy is appropriately adjusted.

The content of the above compound is, for example, 3 to 60% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Alternatively, in another embodiment of the present invention, the content is 4 to 60% by mass. Further, in another embodiment of the present invention, the content is 15 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 25 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 30 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 35 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 38 to 60% by mass. Furthermore, In another embodiment of the present invention, the content is 40 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 42 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 45 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 47 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 50 to 60% by mass.

In addition, the content of the above compound is, for example, 3 to 60% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content is from 3 to 55% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 45% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 30% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 20% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 15% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 5% by mass.

Further, the compound represented by the formula (I-2) is preferably a compound selected from the group of compounds represented by the formula (3.1) to the formula (3.4), more preferably a formula (3.1), a formula (3.3) or A compound represented by the formula (3.4). In particular, the compound represented by the formula (3.2) is preferred because it particularly improves the reaction rate of the liquid crystal composition of the present invention. Further, when the Tni which is required to be high is more preferable than the reaction rate, it is preferred to use a compound represented by the formula (3.3) or the formula (3.4). The content of the compound represented by the formula (3.3) and the formula (3.4) is preferably 20% or more in order to improve the solubility at a low temperature.

Further, the compound represented by the formula (I-2) is preferably a compound selected from the group consisting of compounds represented by the formulae (3.1) to (3.4), preferably a formula (3.1), a formula (3.3) and / or a compound of the formula (3.4).

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (3.3) is preferably 2% by mass or more and 40% by mass or less based on the total mass of the liquid crystal composition of the present invention. More preferably, the content is 3% by mass or more and 40% by mass or less, 4% by mass or more and 40% by mass or less, 10% by mass or more and 40% by mass or less, 12% by mass or more and 40% by mass or less, and 14% by mass or more and 40% by mass. % or less, 16% by mass or more and 40% by mass or less, 20% by mass or more and 40% by mass or less, 23% by mass or more and 40% by mass or less, 26% by mass or more and 40% by mass or less, 30% by mass or more and 40% by mass or less, 34% by mass % or more 40% by mass or less, 37% by mass or more and 40% by mass or less, or 3% by mass or more and 4% by mass or less, 3% by mass or more and 10% by mass or less, 3% by mass or more and 12% by mass or less, and 3% by mass or more and 14% by mass or less % or less, 3% by mass or more and 16% by mass or less, 3% by mass or more and 20% by mass or less, 3% by mass or more and 23% by mass or less, 3% by mass or more and 26% by mass or less, 3% by mass or more and 30% by mass or less, and 3 mass% % or more and 34% by mass or less, 3% by mass or more and 37% by mass or less, and 2% by mass or more and 6% by mass or less.

Among these contents, it is particularly preferably 2% by mass or more and 6% by mass or less.

Further, the compound represented by the formula (I) is preferably a compound selected from the group of compounds represented by the formula (I-3). (wherein R ¹³ represents an alkyl group having 1 to 5 carbon atoms, and R ¹⁵ represents an alkoxy group having 1 to 4 carbon atoms).

The kind of the compound which can be combined is not particularly limited, but the plural number represented by the above formula (I-3) can be combined in accordance with the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Compound. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types. Further, in another embodiment of the present invention, there are three types.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (I-3) must be in accordance with solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, dripping marks, and imprinting. The required performance such as dielectric anisotropy is appropriately adjusted.

The content of the above compound is, for example, 3% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Alternatively, in another embodiment of the present invention, the content is 4 to 60% by mass. Further, in another embodiment of the present invention, the content is 15 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 25 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 30 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 35 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 38 to 60% by mass. Furthermore, in this issue In another embodiment of the invention, the content is 40 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 42 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 45 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 47 to 60% by mass. Furthermore, in another embodiment of the present invention, the content is 50 to 60% by mass.

In addition, the content of the compound is, for example, in one embodiment of the present invention, the content of the compound is from 3 to 60% by mass based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content is from 3 to 55% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 45% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 30% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 20% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 15% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 5% by mass.

When the solubility at a low temperature is emphasized, the effect is high if the content is set slightly, and conversely, when the reaction rate is emphasized, the effect is high if the content is set slightly. Further, in order to improve the dripping trace or the imprinting property, it is preferred to set the range of the content in the middle.

Further, the compound represented by the formula (I-3) is preferably a compound selected from the group consisting of compounds represented by the formulae (4.1) to (4.3), and preferably a compound represented by the formula (4.3).

The content of the compound represented by the formula (4.3) is preferably 2% by mass or more and 30% by mass or less, more preferably 4% by mass or more and 30% by mass or less, and even more preferably 6 or less, based on the total mass of the liquid crystal composition of the present invention. The mass% or more is 30% by mass or less, more preferably 8% by mass or more and 30% by mass or less, more preferably 10% by mass or more and 30% by mass or less, still more preferably 12% by mass or more and 30% by mass or less, and still more preferably 14% by mass or less. 30% by mass or less, more preferably 16% by mass or more and 30% by mass or less, still more preferably 18% by mass or more and 25% by mass or less, more preferably 20% by mass or more and 24% by mass or less, and particularly preferably 22% by mass or more and 23 or more Below mass%.

Further, the compound represented by the formula (I) is preferably a compound selected from the group of compounds represented by the formula (I-4). (wherein R ¹¹ and R ¹² each independently represent an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 4 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The kind of the compound which can be combined is not particularly limited, but the plural number represented by the above formula (I-4) can be combined in accordance with the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Compound. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types.

In the liquid crystal composition of the present invention, the formula (I-4) The content of the compound must be appropriately adjusted in accordance with the properties required for solubility at low temperature, transition temperature, electronic reliability, birefringence, process suitability, dripping marks, branding, dielectric anisotropy, and the like.

The content of the above compound is, for example, 3 to 50% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Alternatively, in another embodiment of the present invention, the content is 5 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 6 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 8 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 10 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 12 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 15 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 20 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 25 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 30 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 35 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 40 to 50% by mass.

In addition, the content of the compound is, for example, in one aspect of the present invention, the content of the compound is from 3 to 50% by mass based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content is 3 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is from 3 to 35% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 30% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 20% by mass. Again In another embodiment of the present invention, the content is from 3 to 15% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 10% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 5% by mass.

When a high birefringence is obtained, the effect is high if the content is set slightly, and conversely, when the Tni is high, the effect is high if the content is set slightly. Further, in order to improve the dripping trace or the imprinting property, it is preferred to set the range of the content in the middle.

Further, the compound represented by the formula (I-4) is preferably a compound selected from the group consisting of compounds represented by the formulae (5.1) to (5.4), more preferably a formula (5.4) of the formula (5.2). The compound shown.

The content of the compound represented by the formula (5.3) is preferably from 1% by mass to 30% by mass, more preferably from 2% by mass to 20% by mass, even more preferably 2, based on the total mass of the liquid crystal composition of the present invention. The mass% or more is 10% by mass or less, and particularly preferably 3% by mass or more and 7% by mass or less. In the range of 3% by mass or more and 5% by mass or less, and 5% by mass or more and 7% by mass or less.

The content of the compound represented by the formula (5.4) is preferably 2% by mass or more and 30% by mass or less based on the total mass of the liquid crystal composition of the present invention. More preferably, the content is 4% by mass or more and 30% by mass or less. 6% by mass or more and 30% by mass or less, 8% by mass or more and 30% by mass or less, 10% by mass or more and 30% by mass or less, 12% by mass or more and 30% by mass or less, 14% by mass or more and 30% by mass or less, and 16% by mass or more 30% by mass or less, 18% by mass or more and 30% by mass or less, 20% by mass or more and 30% by mass or less, 22% by mass or more and 30% by mass or less, 23% by mass or more and 30% by mass or less, 24% by mass or more and 30% by mass or less, and 24% by mass or more and 30% by mass or less. 25% by mass or more and 30% by mass or less, or 4% by mass or more and 6% by mass or less, 4% by mass or more and 8% by mass or less, 4% by mass or more and 10% by mass or less, 4% by mass or more and 12% by mass or less, and 4% by mass or more. 14% by mass or less, 4% by mass or more and 16% by mass or less, 4% by mass or more and 18% by mass or less, 4% by mass or more and 20% by mass or less, 4% by mass or more and 22% by mass or less, 4% by mass or more and 23% by mass or less, and 4% by mass or more and 23% by mass or less. 4% by mass or more and 24% by mass or less, and 4% by mass or more and 25% by mass or less.

Further, the compound represented by the formula (I) is preferably a compound selected from the group of compounds represented by the formula (I-5). (wherein R ¹¹ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms; and R ¹² represents an alkyl group having 1 to 5 carbon atoms; An alkenyl group having 4 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The kind of the compound which can be combined is not particularly limited, but the plural number represented by the above formula (I-5) can be combined in accordance with the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Compound. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Or in another embodiment of the present invention There are 2 types in the middle.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (I-5) must be in accordance with solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, dripping marks, and imprinting. The required performance such as dielectric anisotropy is appropriately adjusted.

The content of the above compound is, for example, 1 to 50% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Alternatively, in another embodiment of the present invention, the content is 5 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 8 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 11 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 13 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 15 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 17 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 20 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 25 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 30 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 35 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 40 to 50% by mass.

In addition, the content of the above compound is, for example, 1 to 50% in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Further, in another embodiment of the present invention, the content is 1% to 40%. Furthermore, in another embodiment of the present invention, the content is 1 to 35%. Furthermore, in another embodiment of the present invention, the foregoing The amount is 1~30%. Furthermore, in another embodiment of the present invention, the content is 1% to 20%. Furthermore, in another embodiment of the present invention, the content is 1 to 15%. Furthermore, in another embodiment of the present invention, the content is 1% to 10%. Furthermore, in another embodiment of the present invention, the content is 1 to 5%.

When the solubility at a low temperature is emphasized, the effect is high if the content is set slightly, and conversely, when the reaction rate is emphasized, the effect is high if the content is set slightly. Further, in order to improve the dripping trace or the imprinting property, it is preferred to set the range of the content in the middle.

Further, the compound represented by the formula (I-5) is preferably a compound selected from the group consisting of compounds represented by the formulae (6.1) to (6.6), preferably a formula (6.3), a formula (6.4) and A compound of the formula (6.6).

In addition, the content of the compound represented by the formula (6.3) is preferably 2% by mass or more and 30% by mass or less, more preferably 4% by mass or more and 25% by mass or less, based on the total mass of the liquid crystal composition of the present invention. It is 6 mass% or more and 20 mass% or less, and particularly preferably 8 mass% or more and 14 mass% or less. In a particularly preferable range, for example, the content is 8 mass% or more and 11 mass% or less, and 11 mass% or more and 14 mass% or less.

For example, the content of the compound represented by the formula (6.6) is preferably 2% by mass or more and 30% by mass or less, more preferably 4% by mass or more and 30% by mass or less, more preferably the total mass of the liquid crystal composition of the present invention. It is 5% by mass or more and 30% by mass or less, more preferably 6% by mass or more and 30% by mass or less, more preferably 9% by mass or more and 30% by mass or less, still more preferably 12% by mass or more and 30% by mass or less, and still more preferably 14% by mass or less. The mass% or more is 30% by mass or less, more preferably 16% by mass or more and 30% by mass or less, more preferably 18% by mass or more and 25% by mass or less, more preferably 20% by mass or more and 24% by mass or less, and particularly preferably 22% by mass or less. The above 23% by mass or less.

The liquid crystal composition of the present invention may further contain a compound represented by the formula (6.7) and the formula (6.8) as a compound represented by the formula (I-5).

It is preferred to adjust the content of the compound represented by the formula (6.7) in accordance with the properties required for solubility at a low temperature, a transition temperature, an electron reliability, a birefringence, etc., with respect to the total mass of the liquid crystal composition of the present invention. In particular, it is preferable to contain 2% by mass or more of the compound, more preferably 3% by mass or more, more preferably 5% by mass or more, and particularly preferably 7% by mass or more.

Further, the compound represented by the formula (I) is preferably a compound selected from the group of compounds represented by the formula (I-6). (wherein R ¹¹ and R ¹² each independently represent an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 4 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms; and each of X ¹¹ and X ¹² The fluorine atom or the hydrogen atom is independently represented, and any of X ¹¹ or X ¹² is a fluorine atom).

The content of the compound represented by the formula (I-6) is preferably 2% by mass or more and 30% by mass or less, more preferably 4% by mass or more and 30% by mass or less, based on the total mass of the liquid crystal composition of the present invention. It is preferably 5% by mass or more and 30% by mass or less, more preferably 6% by mass or more and 30% by mass or less, more preferably 9% by mass or more and 30% by mass or less, still more preferably 12% by mass or more and 30% by mass or less, and more preferably 14% by mass or more and 30% by mass or less, more preferably 16% by mass or more and 30% by mass or less, more preferably 18% by mass or more and 25% by mass or less, more preferably 20% by mass or more and 24% by mass or less, and particularly preferably 22% by mass or less % or more and 23% by mass or less.

Further, the compound represented by the formula (I-6) is preferably a compound represented by the formula (7.1).

Further, the compound represented by the formula (I) is preferably a compound selected from the group of compounds represented by the formula (I-7). (wherein R ¹¹ and R ¹² each independently represent an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, and X ¹² each independently represents Fluorine or chlorine atom).

The content of the compound represented by the formula (I-7) is preferably from 1% by mass to 30% by mass, more preferably from 2% by mass to 30% by mass, based on the total mass of the liquid crystal composition of the present invention. It is preferably 3 mass% or more and 30 mass% or less, more preferably 4 mass% or more and 30 mass% or less, more preferably 6 mass% or more and 30 mass% or less, still more preferably 8 mass% or more and 30 mass% or less, more preferably 10% by mass or more and 30% by mass or less, more preferably 12% by mass or more and 30% by mass or less, more preferably 15% by mass or more and 25% by mass or less, still more preferably 18% by mass or more and 24% by mass or less, and particularly preferably 21% by mass or less % or more and 22% by mass or less.

Further, the compound represented by the formula (I-7) is preferably a compound represented by the formula (8.1).

Further, the compound represented by the formula (I) is preferably a compound selected from the group of compounds represented by the formula (I-8). (wherein R ¹⁶ and R ¹⁷ each independently represent an alkenyl group having 2 to 5 carbon atoms).

The kind of the compound which can be combined is not particularly limited, but it is preferably a compound represented by the above formula (I-8) in terms of properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Combination of 1 to 3 species in a plurality of compounds. The content of the compound represented by the formula (I-8) is based on solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, dripping trace, branding, dielectric constant The performance required for the numerical anisotropy or the like is preferably 5% by mass or more and 65% by mass or less, more preferably 10% by mass or more and 5% by mass or less, and still more preferably 15% by mass based on the total mass of the liquid crystal composition of the present invention. The mass% or more is 65 mass% or less, more preferably 20 mass% or more and 65 mass% or less, more preferably 25% by mass or more and 65% by mass or less, more preferably 30% by mass or more and 65% by mass or less, and still more preferably 35% by mass. The amount is 65 mass% or less, more preferably 40 mass% or more and 65 mass% or less, more preferably 45 mass% or more and 60 mass% or less, more preferably 50 mass% or more and 58 mass% or less, and particularly preferably 55 mass% or more. Below mass%.

Further, the compound represented by the formula (I-8) is preferably a compound selected from the group consisting of the compounds represented by the formula (9.1) to the formula (9.10), preferably a formula (9.2), a formula (9.4) and a compound of the formula (9.7).

Further, the compound represented by the formula (L) is preferably, for example, a compound selected from the compounds represented by the formula (II). (R ²¹ and R ²² each independently represent an alkenyl group having 2 to 5 carbon atoms, an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, and A ² represents a 1,4-extension ring; Hexyl or 1,4-phenylene, Q ² represents a single bond, -COO-, -CH ₂ -CH ₂ - or -CF ₂ O-).

The kind of the compound which can be combined is not particularly limited, but the compound of the above formula (II) can be combined according to the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. . The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types. Further, in still another embodiment of the present invention, there are three types. Furthermore, in another embodiment of the present invention, it is four or more types.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (II) must be in accordance with solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, dripping marks, branding, and intercalation. The required performance such as electrical anisotropy is suitably adjusted.

The content of the above compound is, for example, 3 to 50% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Alternatively, in another embodiment of the present invention, the content is 5 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 7 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 10 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 14 to 50% by mass. Furthermore, another in the present invention In one embodiment, the content is 16 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 20 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 23 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 26 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 30 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 35 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 40 to 50% by mass.

In addition, the content of the compound is, for example, 3 to 50% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content is 3 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is from 3 to 35% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 30% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 20% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 15% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 10% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 5% by mass.

Further, the compound represented by the formula (II) is preferably, for example, a compound selected from the group of compounds represented by the formula (II-1). (R ²¹ and R ²² each independently represent an alkenyl group having 2 to 5 carbon atoms, an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The content of the compound represented by the formula (II-1) is preferably as per The performance at a low temperature, such as solubility, transition temperature, electronic reliability, and birefringence, is adjusted, and is preferably 4% by mass or more and 24% by mass or less, more preferably 8% by mass or more and 18% by mass or less. It is 12% by mass or more and 14% by mass or less.

Further, the compound represented by the formula (II-1) is preferably a compound represented by the formula (10.1) and the formula (10.2), for example.

Further, the compound represented by the formula (II) is preferably, for example, a compound selected from the group of compounds represented by the formula (II-2). (R ²³ represents an alkenyl group having 2 to 5 carbon atoms, and R ²⁴ represents an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The kind of the compound which can be combined is not particularly limited, but the plural number represented by the above formula (II-2) can be combined in accordance with the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Compound. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, it is two or more types.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (II-2) must be in accordance with solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, dripping marks, and imprinting. The required performance such as dielectric anisotropy is appropriately adjusted.

The content of the above compound is, for example, 3 to 50% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Alternatively, in another embodiment of the present invention, the content is 5 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 7 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 10 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 14 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 16 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 20 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 23 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 26 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 30 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 35 to 50% by mass. Furthermore, in another embodiment of the present invention, the content is 40 to 50% by mass.

In addition, the content of the compound is, for example, 3 to 50% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content is 3 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is from 3 to 35% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 30% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 20% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 15% by mass. Furthermore, in another embodiment of the present invention, the content is 3 to 10% by mass. Furthermore, In another embodiment of the present invention, the content is from 3 to 5% by mass.

Further, the compound represented by the formula (II-2) is preferably, for example, a compound represented by the formula (11.1) to the formula (11.3).

The compound represented by the formula (11.1) may be contained, or the compound represented by the formula (11.2) may be contained, or the formula (11.1) may be contained according to the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Both the compound shown and the compound represented by the formula (11.2) or all of the compounds represented by the formula (11.1) to the formula (11.3). The content of the compound represented by the formula (11.1) or the formula (11.2) is preferably 3% by mass or more and 40% by mass or less, and more preferably 5% by mass or more and 35% by mass or less based on the total mass of the liquid crystal composition of the present invention. In particular, it is preferably 5% by mass or more and 30% by mass or less, particularly preferably 5% by mass or more and 25% by mass or less, and most preferably 5% by mass or more and 20% by mass or less. In addition, in an optimum range, for example, it is 8% by mass or more and 20% by mass or less, 12% by mass or more and 20% by mass or less, 15% by mass or more and 20% by mass or less, 5% by mass or more and 18% by mass or less, and 5 or less. The mass% is 15% by mass or less, 5% by mass or more and 12% by mass or less, 5% by mass or more and 10% by mass or less, and 5% by mass or more and 8% by mass or less.

In addition, the content of the compound represented by the formula (11.1) is preferably 3% by mass or more and 40% by mass or less, more preferably 5% by mass or more and 35% by mass or less, based on the total mass of the liquid crystal composition of the present invention. 5% by mass or more and 30% by mass or less, and particularly preferably 5% by mass or more and 25% by mass or less. It is particularly preferably 5 mass% or more and 20 mass% or less.

In a particularly preferable range, for example, 5% by mass or more and 17% by mass or less, 5% by mass or more and 15% by mass or less, 5% by mass or more and 12% by mass or less, 5% by mass or more and 10% by mass or less, and 5 masses are exemplified. %% or more and 8 mass% or less, 6 mass% or more and 20 mass% or less, 8 mass% or more and 20 mass% or less, 10 mass% or more and 20 mass% or less, 12 mass% or more and 20 mass% or less, 15 mass% or more and 20 mass% or more. Hereinafter, it is 17 mass% or more and 20 mass% or less.

In addition, the content of the compound represented by the formula (11.2) is preferably 3% by mass or more and 40% by mass or less, more preferably 3% by mass or more and 35% by mass or less, based on the total mass of the liquid crystal composition of the present invention. It is 3% by mass or more and 30% by mass or less, more preferably 3% by mass or more and 25% by mass or less, particularly preferably 3% by mass or more and 20% by mass or less, and most preferably 5% by mass or more and 12% by mass or less.

In an optimum range, for example, it is 5% by mass or more and 10% by mass or less, 5% by mass or more and 8% by mass or less, 5% by mass or more and 6% by mass or less, 6% by mass or more, 12% by mass or less, and 8 mass%. The content is 12% by mass or less, 10% by mass or more and 12% by mass or less.

When both the compound represented by the formula (11.1) and the compound represented by the formula (11.2) are contained, the total mass of the compound of the two is preferably 10% by mass based on the total mass of the liquid crystal composition of the present invention. The above 45 mass% or less is more preferably 13% by mass or more and 35% by mass or less, and particularly preferably 16% by mass or more and 25% by mass or less.

In a more preferable range, for example, it is 16 mass% or more and 22 mass% or less, 16 mass% or more, 20 mass% or less, and 16 mass% or more. The content is 5% by mass or less, 18% by mass or more and 25% by mass or less, 20% by mass or more and 25% by mass or less, and 22% by mass or more and 25% by mass or less.

Further, the compound represented by the formula (II) is preferably, for example, a compound selected from the group of compounds represented by the formula (II-3). (R ²⁵ represents an alkyl group having 1 to 5 carbon atoms, and R ²⁴ represents an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The type of the compound which can be combined is not particularly limited, but it is preferably contained in the above formula (II-3) in terms of properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. One to three species of the compound of the plural.

The content of the compound represented by the formula (II-3) must be such as solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, dropping trace, branding, dielectric anisotropy, and the like. The required performance is suitable for adjustment. The content of the liquid crystal composition of the present invention is preferably, for example, 2 to 45% by mass based on the total mass of the liquid crystal composition of the present invention. More preferably, the content is 5 to 45% by mass, 8 to 45% by mass, 11 to 45% by mass, 14 to 45% by mass, 17 to 45% by mass, 20 to 45% by mass, and 23 to 45% by mass. 26 to 45 mass%, 29 to 45 mass%, or 2 to 45 mass%, 2 to 40 mass%, 2 to 35 mass%, 2 to 30 mass%, 2 to 25 mass%, 2 to 20 mass%, 2 ~15% by mass, 2 to 10% by mass.

Further, the compound represented by the formula (II-3) is preferably, for example, a compound represented by the formula (12.1) to the formula (12.3).

The compound represented by the formula (12.1) may be contained, or the compound represented by the formula (12.2) may be contained, or the formula (12.1) may be contained according to the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Both the compound shown and the compound represented by the formula (12.2). The content of the compound represented by the formula (12.1) or the formula (12.2) is preferably 3% by mass or more and 40% by mass or less, more preferably 5% by mass or more and 40% by mass or less based on the total mass of the liquid crystal composition of the present invention. More preferably, it is 7% by mass or more and 40% by mass or less, more preferably 9% by mass or more and 40% by mass or less, still more preferably 11% by mass or more and 40% by mass or less, and still more preferably 12% by mass or more and 40% by mass or less. It is preferably 13% by mass or more and 40% by mass or less, more preferably 18% by mass or more and 30% by mass or less, and particularly preferably 21% by mass or more and 25% by mass or less. In addition, the content of the compound represented by the formula (12.2) is preferably 3% by mass or more and 40% by mass or less, more preferably 5% by mass or more and 40% by mass or less, based on the total mass of the liquid crystal composition of the present invention. It is 8% by mass or more and 40% by mass or less, more preferably 10% by mass or more and 40% by mass or less, particularly preferably 12% by mass or more and 40% by mass or less, particularly preferably 15% by mass or more and 40% by mass or less, and particularly preferably 17% by mass. The mass% or more is 30% by mass or less, and particularly preferably 19% by mass or more and 25% by mass or less. When both the compound represented by the formula (12.1) and the compound represented by the formula (12.2) are contained, the total mass of the compound of the two is preferably 15% by mass based on the total mass of the liquid crystal composition of the present invention. 45 mass% or less, more preferably 19 mass% or more and 45 mass% or less, particularly preferably 24 mass% or more and 40 mass% or less, particularly preferably 30 mass% or more and 35 Below mass%.

In addition, the content of the compound represented by the formula (12.3) is preferably 0.05% by mass or more and 2% by mass or less, more preferably 0.1% by mass or more and 1% by mass or less, based on the total mass of the liquid crystal composition of the present invention. It is 0.2% by mass or more and 0.5% by mass or less. The compound represented by the formula (12.3) may also be an optically active compound.

Further, the compound represented by the formula (II-3) is preferably, for example, a compound selected from the group of compounds represented by the formula (II-3-1). (R ²⁵ represents an alkyl group having 1 to 5 carbon atoms, and R ²⁶ represents an alkoxy group having 1 to 4 carbon atoms).

The kind of the compound which can be combined is not particularly limited, but it is preferably contained in the above formula (II-3-1) in accordance with the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. One to three of the plural compounds shown.

The content of the compound represented by the formula (II-3-1) is preferably adjusted according to the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence, and is preferably 1% by mass. The above is 24 mass% or less, more preferably 4 mass% or more and 18 mass% or less, and particularly preferably 8 mass% or more and 14 mass% or less.

Further, the compound represented by the formula (II-3-1) is preferably a compound represented by the formula (13.1) to the formula (13.4), and particularly preferably a compound represented by the formula (13.3).

Further, the compound represented by the formula (II) is preferably, for example, a compound selected from the group of compounds represented by the formula (II-4). (R ²¹ and R ²² each independently represent an alkenyl group having 2 to 5 carbon atoms, an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

Only one type of these compounds may be contained, or two or more types may be contained, and it is preferable to mix suitably according to the required performance. The kind of the compound which can be combined is not particularly limited, but it is preferably one of these compounds in accordance with the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. The type is particularly good for one to three types.

The content of the compound represented by the formula (II-4) is preferably from 1% by mass to 15% by mass, more preferably from 2% by mass to 15% by mass, based on the total mass of the liquid crystal composition of the present invention. It is preferably 3% by mass or more and 15% by mass or less, more preferably 4% by mass or more and 12% by mass or less, and particularly preferably 5% by mass or more and 7% by mass or less.

Further, the compound represented by the formula (II-4) is preferably a compound represented by the formula (14.1) to the formula (14.5), and particularly preferably a compound represented by the formula (14.2) or the formula (14.5).

Further, the compound represented by the formula (L) is preferably a compound selected from the group of compounds represented by the formula (III). (R ³¹ and R ³² independently represent an alkenyl group having 2 to 5 carbon atoms, an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The content of the compound represented by the formula (III) is preferably 3% by mass or more and 25% by mass or less based on the total mass of the liquid crystal composition of the present invention in consideration of the required solubility or birefringence. More preferably, it is 6% by mass or more and 20% by mass or less, and particularly preferably 8% by mass or more and 15% by mass or less.

Further, the compound represented by the formula (III) is preferably a compound represented by the formula (15.1) or the formula (15.2), and particularly preferably a compound represented by the formula (15.1).

Further, the compound represented by the formula (III) is preferably a compound selected from the group of compounds represented by the formula (III-1). (R ³³ represents an alkenyl group having 2 to 5 carbon atoms, and R ³² each independently represents an alkyl group having 1 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound represented by the formula (III-1) is preferably adjusted in accordance with the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence, and is preferably 4% by mass or more. The mass% or less is more preferably 6% by mass or more and 18% by mass or less, and particularly preferably 10% by mass or more and 13% by mass or less.

The compound represented by the formula (III-1) is preferably a compound represented by the formula (16.1) or the formula (16.2), for example.

Further, the compound represented by the formula (III) is preferably a compound selected from the group of compounds represented by the formula (III-2). (R ³¹ represents an alkyl group having 1 to 5 carbon atoms, and R ³⁴ represents an alkoxy group having 1 to 4 carbon atoms).

The content of the compound represented by the formula (III-2) is preferably such that solubility at low temperature, transition temperature, electron reliability, birefringence, etc. The required performance is adjusted, and is preferably 4% by mass or more and 23% by mass or less, more preferably 6% by mass or more and 18% by mass or less, and still more preferably 10% by mass or more and 13% by mass or less.

In addition, the compound represented by the formula (III-2) is preferably a compound selected from the group consisting of the compounds represented by the formula (17.1) to the formula (17.3), and particularly preferably a compound represented by the formula (17.3).

Further, the compound represented by the formula (L) is preferably selected from the group represented by the formula (IV). (wherein R ⁴¹ and R ⁴² each independently represent an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms, and X ⁴¹ and X ⁴² each independently represent a hydrogen atom or a fluorine atom).

The kind of the compound which can be combined is not particularly limited, but the compound of the above formula (IV) can be combined in accordance with the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. . The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types. Furthermore, in another embodiment of the present invention, there are three types. Furthermore, in another embodiment of the present invention, there are four types. Furthermore, In another embodiment of the present invention, there are five types. Furthermore, in another embodiment of the present invention, it is six or more types.

Further, the compound represented by the formula (IV) is preferably, for example, a compound selected from the group of compounds represented by the formula (IV-1). (wherein R ⁴³ and R ⁴⁴ each independently represent an alkyl group having 1 to 5 carbon atoms).

The content of the compound represented by the formula (IV-1) must be such as solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, dropping trace, branding, dielectric anisotropy, and the like. The required performance is suitable for adjustment.

The content of the above compound is, for example, 1 to 40% by mass based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content is 2 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 4 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 6 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 8 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 10 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 12 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 15 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 18 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 21 to 40% by mass.

Further, for example, in one embodiment of the present invention, the content of the compound is from 1 to 40% by mass based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content is 1 to 30% by mass. Furthermore, in another embodiment of the present invention, the content is 1 to 25% by mass. Furthermore, in another embodiment of the present invention, the content is 1 to 20% by mass. Furthermore, in another embodiment of the present invention, the content is 1 to 15% by mass. Furthermore, in another embodiment of the present invention, the content is 1 to 10% by mass. Furthermore, in another embodiment of the present invention, the content is 1 to 5% by mass. Furthermore, in another embodiment of the present invention, the content is 1 to 4% by mass.

Further, the compound represented by the formula (IV-1) is preferably a compound represented by the formula (18.1) to the formula (18.9), for example.

The type of the compound which can be combined is not particularly limited, but it is preferably one to three kinds of these compounds, and more preferably one to four. Further, since the molecular weight distribution of the selected compound is also effective in solubility, for example, one of the compounds represented by the formula (18.1) or (18.2), and the formula (18.4) or (18.5) are preferably selected. One of the compounds shown in the above formula, one of the compounds represented by the formula (18.6) or the formula (18.7), and one of the compounds represented by the formula (18.8) or (18.9) are appropriately combined. Among them, a compound represented by the formula (18.1), the formula (18.3) (18.4), the formula (18.6), and the formula (18.9) is preferably contained.

Further, the compound represented by the formula (IV) is preferably, for example, a compound selected from the group of compounds represented by the formula (IV-2). (wherein R ⁴⁵ and R ⁴⁶ each independently represent an alkyl group having 1 to 5 carbon atoms or an alkenyl group having 2 to 5 carbon atoms; and at least one of the alkenyl groups having 2 to 5 carbon atoms; X ⁴¹ and X ⁴² each independently represents a hydrogen atom or a fluorine atom).

The kind of the compound which can be combined is not particularly limited, but the compound represented by the above formula (IV-2) can be combined in accordance with the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Number of compounds.

The content of the compound represented by the formula (IV-2) must be such as solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, dropping trace, branding, dielectric anisotropy, and the like. The required performance is suitable for adjustment. For example, the content of the above compound is preferably from 0.5 to 40% by mass based on the total mass of the liquid crystal composition of the present invention. More preferably, the content is 1 to 40% by mass, 2 to 40% by mass, 3 to 40% by mass, 5 to 40% by mass, 7 to 40% by mass, 9 to 40% by mass, and 12 to 40% by mass. 15 to 40% by mass, 20 to 40% by mass, or 1 to 40% by mass, 1 to 30% by mass, 1 to 25% by mass, 1 to 20% by mass, 1 to 15% by mass, 1 to 10% by mass, 1 ~5 mass%, 1 to 4 mass%.

Further, the compound represented by the formula (IV-2) is preferably a compound represented by the formula (19.1) to the formula (19.8), and among them, a compound represented by the formula (19.2) is preferred.

As a component of the liquid crystal composition, since the molecular weight distribution of the selected compound is broad and effective for solubility, for example, one of the compounds represented by the formula (19.1) or (19.2) and the formula (19.3) are preferably selected. Or one of the compounds represented by the formula (19.5), one of the compounds of the formula (19.5) or the formula (19.6), and one of the compounds of the formula (19.7) or (19.8) It is appropriate to combine these.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (19.2) is considered in view of solubility at low temperature, transition temperature, electron reliability, etc., and is preferably based on the total mass of the liquid crystal composition of the present invention. It is 0.5% by mass or more and 15% by mass or less, more preferably 1% by mass or more and 10% by mass or less, and particularly preferably 1% by mass or more and 7% by mass or less, particularly preferably 1% by mass or more and 5% by mass or less, and most preferably 1% by mass or less. The mass% or more is 3% by mass or less.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (19.4) is preferably a solubility at a low temperature, a transition temperature, an electron reliability, etc., and is preferably based on the total mass of the liquid crystal composition of the present invention. It is 3% by mass or more and 25% by mass or less, more preferably 5% by mass or more and 20% by mass or less, and particularly preferably 5% by mass or more and 15% by mass or less, and particularly preferably 7% by mass or more and 10% by mass or less.

Further, the compound represented by the formula (L) is preferably a compound selected from the group represented by the formula (V). (wherein R ⁵¹ and R ⁵² each independently represent an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms; and each of A ⁵¹ and A ⁵² Independently, it represents 1,4-cyclohexylene or 1,4-phenylene, Q ⁵ represents a single bond or -COO-, and X ⁵¹ and X ⁵² each independently represent a fluorine atom or a hydrogen atom).

The kind of the compound which can be combined is not particularly limited, but the compound of the above formula (V) can be combined according to the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. . The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types. Furthermore, in another embodiment of the present invention, there are three types. Furthermore, in another embodiment of the present invention, there are four types.

The content of the above compound is, for example, 2 to 40% by mass based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content is 4 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 7 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 10 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 12 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 15 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 17 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 18 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 20 to 40% by mass. Furthermore, in another embodiment of the present invention, the content is 22 to 40. quality%.

Further, for example, in one embodiment of the present invention, the content of the compound is from 2 to 40% by mass based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content of the compound is from 2 to 30% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is 2 to 25% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is 2 to 20% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is from 2 to 15% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is from 2 to 10% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is 2 to 5% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is from 2 to 4% by mass.

Further, the compound represented by the formula (V) is preferably a compound represented by the formula (V-1). (wherein R ⁵¹ and R ⁵² each independently represent an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms; and each of X ⁵¹ and X ⁵² Independently represents a fluorine atom or a hydrogen atom).

Further, the compound represented by the formula (V-1) is preferably a compound represented by the formula (V-1-1). (wherein R ⁵¹ and R ⁵² each independently represent an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The total mass of the liquid crystal composition of the present invention is preferably from 1% by mass to 15% by mass, based on the compound represented by the formula (V-1-1), and particularly preferably from 2% by mass to 15% by mass. In the following, it is particularly preferably 3% by mass or more and 10% by mass or less, and particularly preferably 4% by mass or more and 8% by mass or less.

Further, the compound represented by the formula (V-1-1) is preferably a compound represented by the formula (20.1) to the formula (20.4), more preferably a compound represented by the formula (20.2).

Further, the compound represented by the formula (V-1) is preferably a compound represented by the formula (V-1-2). (wherein R ⁵¹ and R ⁵² each independently represent an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The total mass of the liquid crystal composition of the present invention is preferably from 1% by mass to 15% by mass, based on the compound represented by the formula (V-1-2), more preferably from 2% by mass to 15% by mass. Below, especially good It is preferably 3% by mass or more and 10% by mass or less, and particularly preferably 4% by mass or more and 8% by mass or less.

Further, the compound represented by the formula (V-1-2) is preferably a compound represented by the formula (21.1) to the formula (21.3), more preferably a compound represented by the formula (21.1).

Further, the compound represented by the formula (V-1) is preferably a compound represented by the formula (V-1-3). (wherein R ⁵¹ and R ⁵² each independently represent an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The total mass of the liquid crystal composition of the present invention is preferably from 1% by mass to 15% by mass, based on the compound represented by the formula (V-1-3), and particularly preferably from 2% by mass to 15% by mass. In the following, it is particularly preferably 3% by mass or more and 10% by mass or less, and particularly preferably 4% by mass or more and 8% by mass or less.

Further, the compound represented by the formula (V-1-3) is a compound represented by the formula (22.1) to the formula (22.3). A compound represented by the formula (22.1) is preferred.

Further, the compound represented by the formula (V) is preferably a compound represented by the formula (V-2). (wherein R ⁵¹ and R ⁵² each independently represent an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms; and each of X ⁵¹ and X ⁵² Independently represents a fluorine atom or a hydrogen atom).

The kind of the compound which can be combined is not particularly limited, but the plural number represented by the above formula (V-2) can be combined in accordance with the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Compound. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, it is two or more types.

The content of the above compound is, for example, 2 to 40% by mass based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content of the compound is 4 to 40% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is from 7 to 40% by mass. Furthermore, another aspect of the present invention In the embodiment, the content of the compound is from 10 to 40% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is from 12 to 40% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is 15 to 40% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is from 17 to 40% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is from 18 to 40% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is from 20 to 40% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is from 22 to 40% by mass.

Further, for example, in one embodiment of the present invention, the content of the compound is from 2 to 40% by mass based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content of the compound is from 2 to 30% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is 2 to 25% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is 2 to 20% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is from 2 to 15% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is from 2 to 10% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is 2 to 5% by mass. Furthermore, in another embodiment of the present invention, the content of the compound is from 2 to 4% by mass.

When it is desired that the liquid crystal composition of the present invention is in the form of a high Tni, it is preferred that the content of the compound represented by the formula (V-2) is slightly larger, and in the case of a low viscosity embodiment, it is preferred to To be less.

Further, the compound represented by the formula (V-2) is preferably a compound represented by the formula (V-2-1). (wherein R ⁵¹ and R ⁵² each independently represent an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

Further, the compound represented by the formula (V-2-1) is preferably a compound represented by the formula (23.1) to the formula (23.4), and preferably a compound represented by the formula (23.1) or the formula (23.2).

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (23.1) is considered to be solubility at a low temperature, a transition temperature, an electron reliability, etc., and is preferably based on the total mass of the liquid crystal composition of the present invention. It is 1% by mass or more and 25% by mass or less, more preferably 1% by mass or more and 15% by mass or less, and particularly preferably 1% by mass or more and 10% by mass or less, and particularly preferably 3% by mass or more and 8% by mass or less.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (23.2) is considered in consideration of solubility at low temperature, transition temperature, electron reliability, etc., relative to the total mass of the liquid crystal composition of the present invention, relative to It is 1% by mass or more and 25% by mass or less, more preferably 1% by mass or more and 15% by mass or less, and particularly preferably 1% by mass or more and 10% by mass or less, particularly preferably 3% by mass or more and 8% by mass or less.

In the liquid crystal composition of the present invention, the total content of the compound represented by the formula (23.1) and the compound represented by the formula (23.2) is considered in consideration of solubility at low temperature, transition temperature, electron reliability, and the like, with respect to the present invention. The total mass of the liquid crystal composition is preferably 1% by mass or more and 25% by mass or less, more preferably 3% by mass or more and 20% by mass or less, particularly preferably 6% by mass or more and 15% by mass or less, and particularly preferably 8% by mass or less. The above 12% by mass or less.

Further, the compound represented by the formula (V-2) is preferably a compound represented by the formula (V-2-2). (wherein R ⁵¹ and R ⁵² each independently represent an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

Further, the compound represented by the formula (V-2-2) is preferably a compound represented by the formula (24.1) to the formula (24.4), and preferably a compound represented by the formula (24.1) or the formula (24.2).

Further, the compound represented by the formula (V) is preferably a compound represented by the formula (V-3). (wherein R ⁵¹ and R ⁵² each independently represent an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The kind of the compound which can be combined is not particularly limited, but the plural number represented by the above formula (V-3) can be combined in accordance with the required properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Compound. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types. Furthermore, in another embodiment of the present invention, it is three or more types.

The compound represented by the formula (V-3) is preferably contained in an amount of 2% by mass or more and 16% by mass or less, and more preferably 4% by mass or more and 16% by mass or less, based on the total mass of the liquid crystal composition of the present invention. In particular, it is preferably 7 mass% or more and 13 mass% or less, and particularly preferably 8 mass% or more and 11 mass% or less.

Further, the compound represented by the formula (V-3) is preferably a compound represented by the formula (25.1) to the formula (25.3).

The liquid crystal composition of the present invention may further contain one or more types of compounds represented by the formula (VI). (wherein R ⁶¹ and R ⁶² each independently represent a linear alkyl group having 1 to 10 carbon atoms, a linear alkoxy group having 1 to 10 carbon atoms or a linear alkenyl group having 2 to 10 carbon atoms) .

The type of the compound which can be combined is not particularly limited, but it is preferably a complex number represented by the above formula (VI) in terms of properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. One to three types of the compounds are more preferably one to four, and particularly preferably one to five. Further, the ratio which can be contained at the maximum is preferably 35% by mass or less, more preferably 25% by mass or less, and still more preferably 15% by mass or less.

As the compound represented by the formula (VI), specifically, the compounds listed below can be suitably used.

The liquid crystal composition of the present invention may further contain one or two or more kinds of compounds represented by the formula (VII). (wherein R ⁷¹ and R ⁷² each independently represent a linear alkyl group having 1 to 10 carbon atoms, a linear alkoxy group having 1 to 10 carbon atoms or a linear alkenyl group having 4 to 10 carbon atoms) .

The type of the compound which can be combined is not particularly limited, but it is preferably a compound having the above formula (VII) in terms of solubility at a low temperature, a transition temperature, an electron reliability, a birefringence or the like. One to three types of the compounds are more preferably one to four, and particularly preferably one to five. Further, the ratio which can be contained at the maximum is preferably 35% by mass or less, more preferably 25% by mass or less, and still more preferably 15% by mass or less.

The compound represented by the formula (VII) can be suitably used as the compound exemplified below.

The liquid crystal composition of the present invention is preferably one or more selected from the group consisting of compounds represented by the formula (M). (wherein R ^M1 represents an alkyl group having 1 to 8 carbon atoms, and one of the alkyl groups or two or more non-adjacent -CH ₂ - groups may independently be -CH=CH-, -C ≡C-, -O-, -CO-, -COO- or -OCO-substituted, PM represents 0, 1, 2, 3 or 4, and C ^M1 and C ^M2 are each independently selected from (d) 1, 4 - a cyclohexyl group (one -CH ₂ - or two or more -CH ₂ - which are not adjacent in this group may be substituted into -O- or -S-) and (e) 1,4-phenylene a group in the group consisting of one (CH============================================================================ One or more hydrogen atoms in the group may be independently substituted by a cyano group, a fluorine atom or a chlorine atom, and K ^M1 and K ^M2 each independently represent a single bond, -CH ₂ CH ₂ -, -(CH _{2 ) 4} -, -OCH ₂ -, -CH ₂ O-, -OCF ₂ -, -CF ₂ O-, -COO-, -OCO- or -C≡C-, when PM is 2, 3 or 4 and K ^{When the} plural of ^M1 is present, they may be the same or different. When PM is 2, 3 or 4 and the complex of C ^M2 is present, they may be the same or different, and X ^M1 and X ^M3 each independently represent a hydrogen atom, Chlorine or fluorine atom, X ^M2 represents a hydrogen atom, a fluorine atom or a chlorine atom , cyano, trifluoromethyl, fluoromethoxy, difluoromethoxy, trifluoromethoxy or 2,2,2-trifluoroethyl; however, the compound of the formula (i) Except for the compound represented by formula (ii)).

The kind of the compound which can be combined is not particularly limited, but the plural number represented by the above formula (M) can be combined in accordance with the desired properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Compound. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types. Furthermore, in another embodiment of the present invention, there are three types. Furthermore, in another embodiment of the present invention, there are four types. Furthermore, in another embodiment of the present invention, there are five types. Furthermore, in another embodiment of the present invention, there are six types. Furthermore, in another embodiment of the present invention There are 7 or more types in the state.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (M) must be in accordance with solubility at low temperature, transition temperature, electronic reliability, birefringence, process suitability, dripping marks, branding, and intercalation. The required performance such as electrical anisotropy is suitably adjusted.

The content of the above compound is, for example, 1 to 95% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Further, for example, in another embodiment of the present invention, the content of the compound is from 10 to 95% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 20 to 95% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 30 to 95% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 40 to 95% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 45 to 95% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 50 to 95% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 55 to 95% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 60 to 95% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 65 to 95% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 70 to 95% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 75 to 95% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 80 to 95% by mass.

Further, with respect to the total mass of the liquid crystal composition of the present invention, The content of the above compound is, for example, 1 to 95% by mass in one embodiment of the present invention. Furthermore, in another embodiment of the present invention, the content of the compound is from 1 to 85% by mass. In still another embodiment of the present invention, the content of the compound is from 1 to 75% by mass. In still another embodiment of the present invention, the content of the compound is from 1 to 65% by mass. In still another embodiment of the present invention, the content of the compound is from 1 to 55% by mass. In still another embodiment of the present invention, the content of the compound is from 1 to 45% by mass. In still another embodiment of the present invention, the content of the compound is from 1 to 35% by mass. In still another embodiment of the present invention, the content of the compound is from 1 to 25% by mass.

When the liquid crystal composition of the present invention has a low viscosity and requires a liquid crystal composition having a high reaction rate, it is preferred that the lower limit value is slightly lower and the upper limit value is slightly lower. In addition, when the liquid crystal composition of the liquid crystal composition of the present invention is high and a liquid crystal composition having good temperature stability is required, it is preferable that the lower limit value is slightly lower and the upper limit value is slightly lower. Further, in order to increase the dielectric anisotropy in order to maintain a low driving voltage, it is preferable that the lower limit is slightly higher and the upper limit is slightly higher.

R ^M1 is preferably a linear alkyl group having 1 to 5 carbon atoms and a linear alkoxy group having 1 to 4 carbon atoms when the ring to which the ring is bonded is a phenyl group (aromatic). And an alkenyl group having 4 to 5 carbon atoms, wherein the ring to which the bond is bonded is cyclohexane, meme, and In the case of a saturated ring structure such as an alkane, a linear alkyl group having 1 to 5 carbon atoms, a linear alkoxy group having 1 to 4 carbon atoms, and a linear carbon number of 2 to 5 are preferable. Alkenyl.

When the compound represented by the formula (M) is required to have chemical stability of the liquid crystal composition, it is preferred that the compound has no chlorine atom in its molecule. Furthermore, The compound having a chlorine atom in the liquid crystal composition is preferably 5% or less, preferably 3% or less, preferably 1% or less, preferably 0.5% or less, and preferably substantially not contained. The compound which is not substantially contained, that is, a compound which is not intended to be produced as an impurity in the production of a compound, means that it is only mixed with a liquid crystal composition of a compound containing a chlorine atom.

The compound represented by the formula (M) is preferably, for example, a compound selected from the group of compounds represented by the formula (VIII). (wherein R ⁸ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms; and X ⁸¹ to X ⁸⁵ each independently represent a hydrogen atom or A fluorine atom, Y ⁸ represents a fluorine atom or -OCF ₃ ).

The kind of the compound which can be combined is not particularly limited, but the plural number represented by the above formula (VIII) can be combined according to the desired properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Used as a compound. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types. Furthermore, in another embodiment of the present invention, it is three or more types.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (VIII) must be in accordance with solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, dripping marks, branding, and intercalation. The required performance such as electrical anisotropy is suitably adjusted.

Relative to the total mass of the liquid crystal composition of the present invention, the foregoing The content of the compound is, for example, 2 to 40% by mass in one embodiment of the present invention. Further, for example, in another embodiment of the present invention, the content of the compound is from 4 to 40% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 5 to 40% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 6 to 40% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 7 to 40% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 8 to 40% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 9 to 40% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 10 to 40% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 11 to 40% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 12 to 40% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 14 to 40% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 15 to 40% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 21 to 40% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 23 to 40% by mass.

In addition, the content of the compound is, for example, 2 to 40% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content of the compound is from 2 to 30% by mass. In still another embodiment of the present invention, the content of the compound is from 2 to 25% by mass. In still another embodiment of the present invention, the content of the compound is from 2 to 21% by mass. to In still another embodiment of the present invention, the content of the compound is from 2 to 16% by mass. In still another embodiment of the present invention, the content of the compound is from 2 to 12% by mass. In still another embodiment of the present invention, the content of the compound is from 2 to 8% by mass. In still another embodiment of the present invention, the content of the compound is from 2 to 5% by mass.

When the liquid crystal composition of the present invention has a low viscosity and requires a liquid crystal composition having a high reaction rate, it is preferred that the lower limit value is slightly lower and the upper limit value is slightly lower. Further, when the liquid crystal composition of the liquid crystal composition of the present invention is high and a liquid crystal composition having good temperature stability is required, it is preferred that the lower limit value is slightly lower and the upper limit value is slightly lower. Further, in order to increase the dielectric anisotropy in order to maintain a low driving voltage, it is preferable to make the above-described lower limit value slightly higher and the upper limit value to be slightly higher.

Further, the compound represented by the formula (VIII) is preferably a compound represented by the formula (VIII-1). (In the formula, R ⁸ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The kind of the compound which can be combined is not particularly limited, but the above formula (VIII-1) can be combined according to the desired properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. A plurality of compounds are used. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, it is two or more types.

Further, the compound represented by the formula (VIII-1) is specifically preferably a compound represented by the formula (26.1) to the formula (26.4), preferably a compound represented by the formula (26.1) or the formula (26.2). More preferably, it is a compound represented by the formula (26.2).

The content of the compound represented by the formula (26.1) is preferably a solubility at a low temperature, a transition temperature, an electron reliability, a birefringence, etc., and is preferably 1% by mass or more based on the total mass of the liquid crystal composition of the present invention. 40% by mass or less, more preferably 1% by mass or more and 30% by mass or less, more preferably 1% by mass or more and 20% by mass or less, more preferably 2% by mass or more and 15% by mass or less, still more preferably 2% by mass or more and 10% by mass or more % or less is particularly preferably 2% by mass or more and 9% by mass or less. In a particularly preferable range, for example, 2% by mass or more and 7% by mass or less, 2% by mass or more and 6% by mass or less, 2% by mass or more and 5% by mass or less, 2% by mass or more and 4% by mass or less, and 2 masses are exemplified. % or more 3% by mass or less, 3% by mass or more and 9% by mass or less, 4% by mass or more and 9% by mass or less, 5% by mass or more and 9% by mass or less, and 6% by mass or more and 9% by mass or less.

The content of the compound represented by the formula (26.2) is preferably a solubility at a low temperature, a transition temperature, an electron reliability, a birefringence, etc., and is preferably 2% by mass or more based on the total mass of the liquid crystal composition of the present invention. 40% by mass or less, more preferably 4% by mass or more and 30% by mass or less, more preferably 7% by mass or more and 20% by mass or less, and particularly preferably 7% by mass or more and 15% by mass or less.

In a particularly preferable range, for example, 7 mass% or more and 12 mass% or less, 7 mass% or more and 10 mass% or less, 7 mass% or more and 8 mass% or less, 8 mass% or more and 15 mass% or less, and 10 masses are exemplified. % or more and 15% by mass or less, and 12% by mass or more and 15% by mass or less.

The total content of the compound represented by the formula (26.1) and the compound represented by the formula (26.2) is preferably 5 to 40% by mass, more preferably 10 to 30% by mass based on the total mass of the liquid crystal composition of the present invention. It is preferably 10 to 25% by mass, and particularly preferably 10 to 20% by mass.

Further, the compound represented by the formula (VIII) is preferably a compound represented by the formula (VIII-2). (In the formula, R ⁸ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The kind of the compound which can be combined is not particularly limited, but the combination of the above formula (VIII-2) can be combined according to the desired properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. A plurality of compounds are used. The type of compound used, for example In one embodiment of the present invention, it is one type. Alternatively, in another embodiment of the present invention, there are two types. Alternatively, in still another embodiment of the present invention, it is three or more types.

The content of the compound represented by the formula (VIII-2) is preferably a solubility at a low temperature, a transition temperature, an electron reliability, a birefringence or the like, and is preferably 2.5% by mass or more and 25% by mass or less, preferably 8 The mass% or more is 25% by mass or less, more preferably 10% by mass or more and 20% by mass or less, and particularly preferably 12% by mass or more and 15% by mass or less.

Further, the compound represented by the formula (VIII-2) is preferably a compound represented by the formula (27.1) to the formula (27.4), and preferably a compound represented by the formula (27.2).

Further, the compound represented by the formula (VIII) is preferably a compound represented by the formula (VIII-3). (In the formula, R ⁸ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The kind of the compound which can be combined is not particularly limited, but the combination of the above formula (VIII-3) can be combined according to the desired properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. A plurality of compounds are used. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, it is two or more types.

Further, the compound represented by the formula (VIII-3) is specifically preferably a compound represented by the formula (26.11) to the formula (26.14), preferably a compound represented by the formula (26.11) or the formula (26.12). More preferably, it is a compound represented by the formula (26.12).

Further, the compound represented by the formula (M) is preferably, for example, a compound selected from the group of compounds represented by the formula (IX). However, except for the compound represented by the above formula (i), (wherein R ⁹ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms; and X ⁹¹ and X ⁹² each independently represent a hydrogen atom or A fluorine atom, Y ⁹ represents a fluorine atom, a chlorine atom or -OCF ₃ , and U ⁹ represents a single bond, -COO- or -CF ₂ O-).

The kind of the compound which can be combined is not particularly limited, but the plural number represented by the above formula (IX) can be combined in accordance with the desired properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. Used as a compound. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types. Furthermore, in another embodiment of the present invention, there are three types. Furthermore, in another embodiment of the present invention, there are four types. Furthermore, in another embodiment of the present invention, there are five types. Furthermore, in another embodiment of the present invention, it is six or more types.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (IX) must be in accordance with solubility at low temperature, transition temperature, electron reliability, birefringence, process suitability, dripping marks, branding, and intercalation. The required performance such as electrical anisotropy is suitably adjusted.

The content of the above compound is, for example, 3 to 70% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Furthermore, for example, in another embodiment of the present invention, the foregoing The content of the compound is 5 to 70% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 8 to 70% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 10 to 70% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 12 to 70% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 15 to 70% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 17 to 70% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 20 to 70% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 24 to 70% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 28 to 70% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 30 to 70% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 34 to 70% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 39 to 70% by mass. For example, in still another embodiment of the present invention, the content of the compound is 40 to 70% by mass. For example, in still another embodiment of the present invention, the content of the compound is from 42 to 70% by mass. For example, in still another embodiment of the present invention, the content of the compound is 45 to 70% by mass.

In addition, the content of the compound is, for example, 3 to 70% by mass in one embodiment of the present invention, based on the total mass of the liquid crystal composition of the present invention. Furthermore, in another embodiment of the present invention, the content of the compound is from 3 to 60% by mass. In still another embodiment of the present invention, the content of the compound is from 3 to 55% by mass. In the invention In still another embodiment, the content of the compound is from 3 to 50% by mass. In still another embodiment of the present invention, the content of the compound is from 3 to 45% by mass. In still another embodiment of the present invention, the content of the compound is from 3 to 40% by mass. In still another embodiment of the present invention, the content of the compound is from 3 to 35% by mass. In still another embodiment of the present invention, the content of the compound is from 3 to 30% by mass. In still another embodiment of the present invention, it is 3 to 25% by mass. In still another embodiment of the present invention, the content of the compound is from 3 to 20% by mass. In still another embodiment of the present invention, the content of the compound is from 3 to 15% by mass. In still another embodiment of the present invention, the content of the compound is from 3 to 10% by mass.

When the liquid crystal composition of the present invention has a low viscosity and requires a liquid crystal composition having a high reaction rate, it is preferred that the lower limit value is slightly lower and the upper limit value is slightly lower. Further, when the liquid crystal composition of the liquid crystal composition of the present invention is high and a liquid crystal composition which is less likely to be imprinted is required, it is preferable that the lower limit value is slightly lower and the upper limit value is slightly lower. Further, in order to increase the dielectric anisotropy in order to maintain a low driving voltage, it is preferable that the lower limit is slightly higher and the upper limit is slightly higher.

Further, the compound represented by the formula (IX) is preferably a compound represented by the formula (IX-1). (wherein R ⁹ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms; X ⁹² represents a hydrogen atom or a fluorine atom, and Y ⁹ represents Fluorine atom or -OCF ₃ ).

The kind of the compound which can be combined is not particularly limited, but the above formula (IX-1) can be combined according to the desired properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. A plurality of compounds are used. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types. Furthermore, in another embodiment of the present invention, there are three types. Further, in another embodiment of the present invention, it is four or more types.

Further, the compound represented by the formula (IX-1) is preferably a compound represented by the formula (IX-1-1). (In the formula, R ⁹ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The kind of the compound which can be combined is not particularly limited, but the above formula (IX-1-1) can be combined according to the desired properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence. The compound of the plural is used. The type of the compound to be used is, for example, one type in one embodiment of the present invention. Alternatively, in another embodiment of the present invention, there are two types.

The content of the compound represented by the above formula (IX-1-1) is considered in consideration of solubility at low temperature, transition temperature, electron reliability, birefringence, etc., in accordance with the total mass of the liquid crystal composition of the present invention. Implementation form The state has a preferred upper and lower limits.

The content of the compound is from 1 to 40% by mass in one embodiment, from 1 to 35% by mass in another embodiment, and from 1 to 30% by mass in still another embodiment with respect to the total mass. In still another embodiment, it is 1 to 25% by mass, and in still another embodiment, it is 1 to 10% by mass, and in still another embodiment, it is 1 to 7% by mass, and yet another In the embodiment, it is 1 to 5% by mass.

Further, the compound represented by the above formula (IX-1-1) is preferably a compound represented by the formula (28.1) to the formula (28.5). The liquid crystal composition preferably contains one or two of the compounds represented by the formula (28.3) and the formula (28.5).

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (28.3) is considered to be solubility at a low temperature, a transition temperature, and electrons. The reliability and the like are preferably 1% by mass or more and 30% by mass or less, more preferably 2% by mass or more and 20% by mass or less, and even more preferably 2% by mass or more and 15% by mass or less, based on the total mass of the liquid crystal composition. It is particularly preferably 2% by mass or more and 12% by mass or less, and most preferably 2% by mass or more and 10% by mass or less.

The most preferable range is, for example, 2% by mass or more and 8% by mass or less, 2% by mass or more and 6% by mass or less, 2% by mass or more and 4% by mass or less, 4% by mass or more and 10% by mass or less, and 6% by mass. The content is 10% by mass or less, 8% by mass or more and 10% by mass or less.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (28.5) is considered to be solubility at a low temperature, a transition temperature, an electron reliability, etc., and is preferably 3 with respect to the total mass of the liquid crystal composition. The mass% or more is 25% by mass or less, more preferably 5% by mass or more and 20% by mass or less, and particularly preferably 5% by mass or more and 15% by mass or less, and particularly preferably 5% by mass or more and 12% by mass or less.

In a particularly preferable range, for example, it is 5% by mass or more and 10% by mass or less, 5% by mass or more and 8% by mass or less, 5% by mass or more and 7% by mass or less, 7% by mass or more and 12% by mass or less, and 8 mass%. % or more and 12% by mass or less, and 10% by mass or more and 12% by mass or less.

In the liquid crystal composition of the present invention, the total content of the compound represented by the formula (28.3) and the compound represented by the formula (28.5) is preferably 5% by mass or more and 30% by mass based on the total mass of the liquid crystal composition. In the following, it is more preferably 7% by mass or more and 28% by mass or less, and particularly preferably 9% by mass or more and 26% by mass or less, particularly preferably 11% by mass or more and 24% by mass or less, and most preferably 13% by mass or more and 22% by mass or less.

In the optimum range, for example, 13% by mass or more and 20% by mass may be mentioned. Hereinafter, 13% by mass or more and 18% by mass or less, 13% by mass or more and 16% by mass or less, 13% by mass or more and 14% by mass or less, 14% by mass or more and 22% by mass or less, 16% by mass or more and 22% by mass or less, and 18% by mass or less The content is 22% by mass or less, 20% by mass or more and 22% by mass or less, and 21% by mass or more and 22% by mass or less.

When the liquid crystal composition contains the compound represented by the above formula (28.3) and the compound represented by the above formula (28.5), the relative content of the liquid crystal composition may be a compound represented by the above formula (28.3). The content of the compound represented by the formula (28.5) is large, but from the viewpoint of increasing the Tni of the liquid crystal composition, the content of the compound represented by the above formula (28.5) is preferably large.

Further, the compound represented by the formula (IX-1) is preferably a compound represented by the formula (IX-1-2). (In the formula, R ⁹ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The type of the compound which can be combined is not limited, and it is preferably in the compound of the above formula (IX-1-2) in consideration of solubility at low temperature, transition temperature, electron reliability, birefringence and the like. 1 to 3 combinations, more preferably 1 to 4 combinations.

The content of the compound represented by the formula (IX-1-2) is considered to be solubility at a low temperature, a transition temperature, an electron reliability, and the like, and is preferably 1% by mass based on the total mass of the liquid crystal composition of the present invention. Above 30% by mass In the following, it is more preferably 5% by mass or more and 30% by mass or less, and particularly preferably 8% by mass or more and 30% by mass or less, particularly preferably 10% by mass or more and 25% by mass or less, and particularly preferably 14% by mass or more and 22% by mass or less. It is particularly preferably 16% by mass or more and 20% by mass or less.

Further, the compound represented by the formula (IX-1-2) is preferably a compound represented by the formula (29.1) to the formula (29.4), and preferably a compound represented by the formula (29.2) or the formula (29.4).

Further, the compound represented by the formula (IX) is preferably a compound represented by the formula (IX-2). However, except for the compound represented by the general formula (i), (wherein R ⁹ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms; and X ⁹¹ and X ⁹² each independently represent a hydrogen atom or A fluorine atom, Y ⁹ represents a fluorine atom, a chlorine atom or -OCF ₃ ).

There are no restrictions on the types of compounds that can be combined, but considering solubility at low temperatures, transition temperature, electron reliability, birefringence, etc. It is possible to use a compound of the plural formula represented by the above formula (IX-2) in an appropriate manner for each embodiment. For example, in one embodiment of the present invention, there are one type, and in another embodiment, two types, in another embodiment, three types, and in still another embodiment, four types, and yet another In one embodiment, there are five types, and in still another embodiment, six or more types are combined.

Further, the compound represented by the formula (IX-2) is preferably a compound represented by the formula (IX-2-1). (In the formula, R ⁹ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The type of the compound which can be combined is not limited, but in consideration of solubility at low temperature, transition temperature, electron reliability, birefringence, etc., it is preferably a compound of the plural compound represented by the above formula (IX-2-1). One to three types of combinations.

The content of the compound represented by the formula (IX-2-1) is based on properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence, and has a preferred upper limit value per embodiment. lower limit.

For example, in one embodiment of the present invention, the content of the compound is from 1 to 40% by mass based on the total mass of the liquid crystal composition of the present invention. In another embodiment, the content of the compound is 2 to 40% by mass, and in still another embodiment, the content of the compound is 4 to 40% by mass, and in still another embodiment, the content of the compound is 10 to 40% by mass, and in yet another embodiment, the aforementioned combination In still another embodiment, the content of the compound is from 16 to 40% by mass, and in still another embodiment, the content of the compound is from 21 to 40% by mass.

Further, for example, in one embodiment of the present invention, the content of the compound is from 1 to 40% by mass based on the total mass, and in another embodiment, the content of the compound is from 1 to 35% by mass. In one embodiment, the content of the compound is 1 to 30% by mass, and in still another embodiment, the content of the compound is 1 to 25% by mass. In still another embodiment, the content of the compound is In another embodiment, the content of the compound is from 1 to 20% by mass, and in still another embodiment, the content of the compound is from 1 to 10% by mass, and yet another In one embodiment, the content of the compound is 1 to 7% by mass, and in still another embodiment, the content of the compound is 1 to 5% by mass.

Further, the compound represented by the formula (IX-2-1) is preferably a compound represented by the formula (30.4) of the formula (30.1), and preferably a compound represented by the formula (30.2) of the formula (30.1).

Further, the compound represented by the formula (IX-2) is preferably a compound represented by the formula (IX-2-2). (In the formula, R ⁹ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The type of the compound that can be combined is not limited, and the solubility at low temperature, the transition temperature, the electron reliability, the birefringence, and the like are considered, and it is preferred to combine the above-mentioned general formula (IX-2-2) of one to three types. The plural compounds shown are more preferably one to four species in combination.

The content of the compound represented by the formula (IX-2-2) is based on properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence, and has an upper limit and a lower limit in each embodiment. . For example, in one embodiment of the present invention, the content of the compound is from 1 to 40% by mass based on the total mass of the liquid crystal composition of the present invention, and in another embodiment, the content of the compound is from 2 to 40% by mass. In still another embodiment, the content of the compound is 4 to 40% by mass, and in still another embodiment, the content of the compound is 10 to 40% by mass, and in still another embodiment, The content of the compound is 14 to 40% by mass, and in still another embodiment, the content of the compound is 16 to 40% by mass, and in still another embodiment, the content of the compound is 21 to 40% by mass. .

Further, for example, in one embodiment of the present invention, the content of the compound is from 1 to 40% by mass based on the total mass, and in another embodiment, the content of the compound is from 1 to 35% by mass. In one embodiment, the content of the compound is 1 to 30% by mass, and in still another embodiment, the content of the compound is 1 to 25% by mass, and in still another embodiment, the content of the compound is 1 ~22% by mass, In still another embodiment, the content of the compound is from 1 to 15% by mass, and in still another embodiment, the content of the compound is from 1 to 12% by mass. In still another embodiment, the compound The content is 1 to 8% by mass, and in still another embodiment, the content of the compound is 1 to 4% by mass.

Further, the compound represented by the formula (IX-2-2) is preferably a compound represented by the formula (31.1) to the formula (31.4), more preferably a compound represented by the formula (31.2) to the formula (31.4). More preferably, it is a compound represented by the formula (31.2).

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (31.2) is preferably 1% by mass or more and 35% by mass or less, and more preferably 2% by mass or more based on the total mass of the liquid crystal composition of the present invention. 25 mass% or less is more preferably 3% by mass or more and 20% by mass or less, particularly preferably 3% by mass or more and 15% by mass or less, and most preferably 3% by mass or more and 11% by mass or less.

In an optimum range, for example, it is 3% by mass or more and 8% by mass or less, 3% by mass or more and 6% by mass or less, 3% by mass or more and 4% by mass or less, 4% by mass or more and 11% by mass or less, and 6% by mass or less. The content is 11% by mass or less, 8% by mass or more and 11% by mass or less.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (31.4) is preferably 1% by mass or more and 35% by mass or less, and more preferably 1% by mass or more based on the total mass of the liquid crystal composition of the present invention. 25 quality % or less is more preferably 1% by mass or more and 15% by mass or less, more preferably 2% by mass or more and 10% by mass or less, still more preferably 3% by mass or more and 8% by mass or less, and particularly preferably 3% by mass or more and 6% by mass or less. It is particularly preferably 3% by mass or more and 5% by mass or less.

Further, the compound represented by the formula (IX-2) is preferably a compound represented by the formula (IX-2-3). (In the formula, R ⁹ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The type of the compound which can be combined is not limited, but in consideration of solubility at low temperature, transition temperature, electron reliability, birefringence, etc., it is preferably a compound of the plural compound represented by the above formula (IX-2-3). One to two types of combinations.

The content of the compound represented by the formula (IX-2-3) is considered to be solubility at a low temperature, a transition temperature, an electron reliability, etc., and is preferably 1% by mass based on the total mass of the liquid crystal composition of the present invention. The amount is 30% by mass or less, more preferably 3% by mass or more and 20% by mass or less, and particularly preferably 6% by mass or more and 15% by mass or less, and particularly preferably 8% by mass or more and 10% by mass or less.

Further, the compound represented by the formula (IX-2-3) is preferably a compound represented by the formula (32.1) to the formula (32.4), preferably represented by the formula (32.2) and/or the formula (32.4). Compound.

Further, the compound represented by the formula (IX-2) is preferably a compound represented by the formula (IX-2-4). (In the formula, R ⁹ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The content of the compound represented by the formula (IX-2-4) is considered to be solubility at a low temperature, a transition temperature, an electron reliability, and the like, and is preferably 1% by mass based on the total mass of the liquid crystal composition of the present invention. The amount is 30% by mass or less, more preferably 3% by mass or more and 20% by mass or less, and particularly preferably 6% by mass or more and 15% by mass or less, particularly preferably 8% by mass or more and 10% by mass or less.

Further, the compound represented by the formula (IX-2-4) is preferably a compound represented by the formula (33.1) to the formula (33.5), preferably represented by the formula (33.1) and/or the formula (33.3). Compound.

Further, the compound represented by the formula (IX-2) is preferably a compound represented by the formula (IX-2-5).

(In the formula, R ⁹ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The type of the compound that can be combined is not limited, but the solubility, the transition temperature, the electron reliability, the birefringence, and the like at a low temperature are considered, and the combination of the above formula (IX-2-5) can be suitably combined for each embodiment. A plurality of compounds are used. For example, in one embodiment of the present invention, there are one type, and in another embodiment, two types, and in still another embodiment, three types, and in still another embodiment, four types or more.

The content of the compound represented by the formula (IX-2-5) is based on the properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence, and has an upper limit and a lower limit in each embodiment. . For example, in one embodiment of the present invention, the content of the compound is 4 to 45% by mass based on the total mass of the liquid crystal composition of the present invention, and in another embodiment, the content of the compound is 8 to 45 mass. In still another embodiment, the content of the compound is 12 to 45% by mass, and in still another embodiment, the content of the compound is 21 to 45% by mass. In still another embodiment, the content of the compound is from 30 to 45% by mass, and in still another embodiment, the content of the compound is from 31 to 45% by mass. In yet another embodiment, the content of the compound is It is 34 to 45 mass%. Further, for example, in one embodiment of the present invention, the content of the compound is 4 to 45% by mass based on the total mass, and in another embodiment, the content of the compound is 4 to 40% by mass. In one embodiment, the content of the compound is 4 to 35% by mass, and in still another embodiment, the content of the compound is 4 to 32% by mass. In still another embodiment, the content of the compound is 4 to 22% by mass, in still another embodiment, the content of the compound is 4 to 13% by mass, and in still another embodiment, the content of the compound is 4 to 9% by mass, and further In one embodiment, the content of the compound is 4 to 8% by mass, and in still another embodiment, the content of the compound is 4 to 5% by mass.

When the liquid crystal composition of the present invention has a low viscosity and requires a liquid crystal composition having a high reaction rate, it is preferred that the lower limit value is slightly lower and the upper limit value is slightly lower. Further, when the liquid crystal composition of the liquid crystal composition of the present invention is high and a liquid crystal composition which is less likely to be imprinted is required, it is preferable that the lower limit value is slightly lower and the upper limit value is slightly lower. Further, in order to increase the dielectric anisotropy in order to maintain a low driving voltage, it is preferable that the lower limit is slightly higher and the upper limit is slightly higher.

Further, the compound represented by the formula (IX-2-5) is preferably a compound represented by the formula (34.1) to the formula (34.5), more preferably a formula (34.1), a formula (34.2) or a formula (34.3). And / or a compound represented by the formula (34.5).

Further, the compound represented by the formula (IX) is preferably a compound represented by the formula (IX-3). (wherein R ⁹ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms; and X ⁹¹ and X ⁹² each independently represent a hydrogen atom or A fluorine atom, Y ⁹ represents a fluorine atom, a chlorine atom or -OCF ₃ ).

Further, the compound represented by the formula (IX-3) is preferably a compound represented by the formula (IX-3-1). (In the formula, R ⁹ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The type of the compound which can be combined is not limited, but in consideration of solubility at low temperature, transition temperature, electron reliability, birefringence and the like, it is preferably a compound of the plural compound represented by the above formula (IX-3-1). One to two types of combinations.

The content of the compound represented by the formula (IX-3-1) is considered to be solubility at a low temperature, a transition temperature, an electron reliability, and the like, and is preferably 3% by mass based on the total mass of the liquid crystal composition of the present invention. The amount is 30% by mass or less, more preferably 7% by mass or more and 30% by mass or less, and particularly preferably 13% by mass or more and 20% by mass or less, and particularly preferably 15% by mass or more and 18% by mass or less.

Further, the compound represented by the formula (IX-3-1) is preferably a compound represented by the formula (35.1) to the formula (35.4), preferably represented by the formula (35.1) and/or the formula (35.2). Compound.

Further, the compound represented by the formula (M) is preferably a compound represented by the formula (X). However, the compound represented by the above formula (i) and the compound represented by the formula (ii) are excluded. (wherein, X ¹⁰¹ to X ¹⁰⁴ each independently represent a fluorine atom or a hydrogen atom, Y ¹⁰ represents a fluorine atom, a chlorine atom, -OCF ₃ , Q ¹⁰ represents a single bond or -CF ₂ O-, and R ¹⁰ represents a carbon atom An alkyl group of 1 to 5, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms, and A ¹⁰¹ and A ¹⁰² each independently represent a 1,4-cyclohexylene group and a 1,4-stretching group. Phenyl or ,or However, the hydrogen atom on the 1,4-phenylene group may be replaced by a fluorine atom).

The compound which can be combined is not particularly limited, but a compound at a low temperature, a transition temperature, an electron reliability, a birefringence or the like can be considered, and a plurality of compounds represented by the above formula (X) are suitably combined for each embodiment. For example, in one embodiment of the present invention, it is one type. Further, in another embodiment of the present invention, there are two types. In still another embodiment, there are three types. In still another embodiment, there are four types. More yet another In the embodiment, it is five or more types.

The content of the compound represented by the formula (X) is in consideration of properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence, and has an upper limit and a lower limit in each embodiment. For example, in one embodiment of the present invention, the content of the compound is 2 to 45% by mass based on the total mass of the liquid crystal composition of the present invention, and in another embodiment, the content of the compound is 3 to 45 mass. In still another embodiment, the content of the compound is 6 to 45% by mass, and in still another embodiment, the content of the compound is 8 to 45% by mass, and in still another embodiment, The content of the compound is from 9 to 45% by mass. In still another embodiment, the content of the compound is from 11 to 45% by mass. In still another embodiment, the content of the compound is from 12 to 45% by mass. . In still another embodiment, the content of the compound is from 18 to 45% by mass. In still another embodiment, the content of the compound is from 19 to 45% by mass. In still another embodiment, the content of the compound is from 23 to 45% by mass. In still another embodiment, the content of the compound is from 25 to 45% by mass. Further, for example, in one embodiment of the present invention, the content of the compound is 2 to 45% by mass based on the total mass, and in another embodiment, the content of the compound is 2 to 35% by mass. In one embodiment, the content of the compound is 2 to 30% by mass, and in still another embodiment, the content of the compound is 2 to 25% by mass. In still another embodiment, the content of the compound is 2 to 20% by mass, in still another embodiment, the content of the compound is 2 to 13% by mass, and in still another embodiment, the content of the compound is 2 to 9% by mass, and yet another In one embodiment, the foregoing The content of the compound is 2 to 6% by mass, and in still another embodiment, the content of the compound is 2 to 3% by mass.

When the liquid crystal composition of the present invention has a low viscosity and requires a liquid crystal composition having a high reaction rate, it is preferred that the lower limit value is slightly lower and the upper limit value is slightly lower. Further, in the case where a liquid crystal composition which is less likely to be imprinted is required, it is preferable that the lower limit value is slightly lower and the upper limit value is slightly lower. Further, in order to increase the dielectric anisotropy in order to maintain a low driving voltage, it is preferable that the lower limit is slightly higher and the upper limit is slightly higher.

The compound represented by the formula (X) used in the liquid crystal composition of the present invention is preferably a compound represented by the formula (X-3). (wherein, X ¹⁰² to X ¹⁰³ each independently represent a fluorine atom or a hydrogen atom, and R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkane having 1 to 4 carbon atoms; Oxy).

The compound which can be combined is not particularly limited, but it is preferably one of the plural compounds represented by the above formula (X-3) in consideration of solubility at low temperature, transition temperature, electron reliability, birefringence and the like. Kind to more than 2 types of combinations.

In addition, the compound represented by the formula (X-3) used in the liquid crystal composition of the present invention is preferably a compound represented by the formula (X-3-1). (In the formula, R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but in view of solubility at low temperature, transition temperature, electron reliability, birefringence and the like, it is preferably a compound of the plural compound represented by the above formula (X-3-1). One to two types or more combinations.

The content of the compound represented by the formula (X-3-1) is preferably 1% by mass or more, more preferably 2% by mass or more, and particularly preferably 3% by mass based on the total mass of the liquid crystal composition of the present invention. the above. Further, in consideration of solubility at low temperature, transition temperature, electronic reliability, and the like, the maximum ratio is preferably limited to 10% by mass or less, more preferably 8% by mass or less, still more preferably 6% by mass or less, and particularly preferably 4% by mass. the following.

Further, the compound represented by the formula (X-3-1) used in the liquid crystal composition of the present invention is specifically preferably a compound represented by the formula (41.1) to the formula (41.4), preferably containing A compound represented by the formula (41.2).

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (41.2) is preferably 0.5% by mass or more and 15% by mass or less, more preferably 1% by mass based on the total mass of the liquid crystal composition of the present invention. The above 10% by mass or less is particularly preferably 1% by mass or more and 7% by mass or less, particularly preferably 1% by mass or more and 5% by mass or less, and most preferably 1% by mass or more and 3% by mass or less.

Further, the compound represented by the formula (X) is preferably a compound represented by the formula (X-4). (In the formula, X ¹⁰² represents a fluorine atom or a hydrogen atom, and R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but it is preferably one of the plural compounds represented by the above formula (X-4) in consideration of solubility at low temperature, transition temperature, electron reliability, birefringence and the like. The combination is more than two types, and more preferably one to three or more types.

In addition, the compound represented by the formula (X-4) used in the liquid crystal composition of the present invention is preferably a compound represented by the formula (X-4-1). (In the formula, R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but in view of solubility at low temperature, transition temperature, electron reliability, birefringence and the like, it is preferably a compound of the plural compound represented by the above formula (X-4-1). The combination of one type to two types or more is more preferably one type to three types or more.

The content of the compound represented by the formula (X-4-1) is preferably 2% by mass or more based on the total mass of the liquid crystal composition of the present invention in consideration of solubility at a low temperature, a transition temperature, and electron reliability. 20% by mass or less, more preferably 5% by mass or more and 17% by mass or less, even more preferably 10% by mass or more and 15% by mass or less, and particularly preferably 10% by mass or more and 13% by mass or less.

Further, the compound represented by the formula (X-4-1) used in the liquid crystal composition of the present invention is specifically preferably a compound represented by the formula (42.1) to the formula (42.4), and preferably contains A compound represented by the formula (42.3).

Further, the compound represented by the formula (X) used in the liquid crystal composition of the present invention is preferably a compound represented by the formula (X-4-2). (In the formula, R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but in view of solubility at low temperature, transition temperature, electron reliability, birefringence and the like, it is preferably a compound of the plural compound represented by the above formula (X-4-2). The combination of one type to two types or more is more preferably one type to three types or more.

The content of the compound represented by the formula (X-4-2) is preferably 2% by mass or more based on the total mass of the liquid crystal composition of the present invention in consideration of solubility at a low temperature, a transition temperature, and electron reliability. 20% by mass or less, more preferably 5% by mass or more and 17% by mass or less, even more preferably 10% by mass or more and 15% by mass or less, and particularly preferably 10% by mass or more and 13% by mass or less.

Further, the compound represented by the formula (X-4-2) used in the liquid crystal composition of the present invention is specifically preferably a compound represented by the formula (42.11) to the formula (42.14), more preferably containing A compound of the formula (42.13) or the formula (42.14).

Further, the compound represented by the formula (X) used in the liquid crystal composition of the present invention is preferably a compound represented by the formula (X-4-3). (In the formula, R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but in view of solubility at low temperature, transition temperature, electron reliability, birefringence and the like, it is preferably a compound of the plural compound represented by the above formula (X-4-3). The combination of one type to two types or more is more preferably one type to three types or more.

The content of the compound represented by the formula (X-4-3) is preferably 2% by mass or more based on the total mass of the liquid crystal composition of the present invention in consideration of solubility at a low temperature, a transition temperature, and electron reliability. 20% by mass or less, more preferably 5% by mass or more and 17% by mass or less, even more preferably 10% by mass or more and 15% by mass or less, and particularly preferably 10% by mass or more and 13% by mass or less.

Further, the compound represented by the formula (X-4-3) used in the liquid crystal composition of the present invention is specifically preferably a compound represented by the formula (42.21) to the formula (42.24), more preferably containing A compound of the formula (42.22).

Further, the compound represented by the formula (X) is preferably a compound represented by the formula (X-5). (In the formula, X ¹⁰² represents a fluorine atom or a hydrogen atom, and R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but it is preferably one of the plural compounds represented by the above formula (X-5) in consideration of solubility at low temperature, transition temperature, electron reliability, birefringence and the like. The combination is more than two types, and more preferably one to three or more types.

In addition, the compound represented by the formula (X-5) used in the liquid crystal composition of the present invention is preferably a compound represented by the formula (X-5-1). (In the formula, R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but in view of solubility at low temperature, transition temperature, electron reliability, birefringence and the like, it is preferably a compound of the plural compound represented by the above formula (X-5-1). The combination of one type to two types or more is more preferably one type to three types or more.

Further, the compound represented by the formula (X-5-1) used in the liquid crystal composition of the present invention is specifically preferably a compound represented by the formula (43.1) to the formula (43.4), and preferably contains a compound. A compound represented by the formula (43.2).

Further, the liquid crystal compound of the present invention may further contain a compound represented by the formula (X'-7) similar to the compound represented by the above formula (X). (In the formula, R ¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but in view of solubility at low temperature, transition temperature, electron reliability, birefringence and the like, it is preferably a compound of the plural compound represented by the above formula (X'-7). One type to two or more types combination.

The content of the compound represented by the formula (X'-7) is in consideration of properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence, and has an upper limit and a lower limit in each embodiment.

For example, in one embodiment of the present invention, the content of the compound is 4 to 30% by mass based on the total mass of the liquid crystal composition of the present invention, and 5 to 30% by mass in another embodiment. In one embodiment, it is 6 to 30% by mass, and in still another embodiment, it is 8 to 30% by mass, and in still another embodiment, it is 9 to 30% by mass. In still another embodiment, 11 to 30% by mass, and in still another embodiment, 14 to 30% by mass. In still another embodiment, it is 18 to 30% by mass.

Further, for example, in one embodiment of the present invention, the content of the compound is 4 to 30% by mass based on the total mass, and in another embodiment, the content of the compound is 4 to 20% by mass. In one embodiment, the content of the compound is 4 to 13% by mass, and in still another embodiment, the content of the compound is 4 to 10% by mass. In still another embodiment, the content of the compound is 4 to 7 mass%.

Further, the compound represented by the formula (X'-7) used in the liquid crystal composition of the present invention is specifically preferably a compound represented by the formula (44.11) to the formula (44.14), and more preferably a formula. (44.13) The compound shown.

Further, the compound represented by the formula (X) is preferably a compound selected from the group represented by the formula (XI). (wherein, X ¹¹¹ to X ¹¹⁷ each independently represent a fluorine atom or a hydrogen atom, at least one of X ¹¹¹ to X ¹¹⁷ represents a fluorine atom, and R ¹¹⁰ represents an alkyl group having 1 to 5 carbon atoms, and 2 to 2 carbon atoms; An alkenyl group of 5 or an alkoxy group having 1 to 4 carbon atoms, and Y ¹¹ represents a fluorine atom or -OCF ₃ ).

The compound which can be combined is not particularly limited, but solubility at low temperature, transition temperature, electron reliability, birefringence, etc. are considered. It is preferred to combine one to three or more of the plurality of compounds represented by the above formula (XI).

The content of the compound represented by the formula (XI) is based on properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence, and has an upper limit and a lower limit in each embodiment. For example, in one embodiment of the present invention, the content of the compound is 2 to 30% by mass based on the total mass of the liquid crystal composition of the present invention, and in another embodiment, the content of the compound is 4 to 30% by mass. In still another embodiment, the content of the compound is 5 to 30% by mass, and in still another embodiment, the content of the compound is 7 to 30% by mass, and in yet another embodiment, The content of the compound is 9 to 30% by mass, and in still another embodiment, the content of the compound is 10 to 30% by mass, and in still another embodiment, the content of the compound is 12 to 30% by mass. . In still another embodiment, the content of the compound is from 13 to 30% by mass. In still another embodiment, the content of the compound is 15 to 30% by mass. In still another embodiment, the content of the compound is from 18 to 30% by mass.

Further, for example, in one embodiment of the present invention, the content of the compound is 2 to 30% by mass based on the total mass, and in another embodiment, the content of the compound is 2 to 25% by mass. In one embodiment, the content of the compound is 2 to 20% by mass, and in still another embodiment, the content of the compound is 2 to 15% by mass. In still another embodiment, the content of the compound is In another embodiment, the content of the compound is 2 to 5% by mass.

When the liquid crystal composition of the present invention is used for a liquid crystal display device having a small liquid crystal layer gap, the content of the compound represented by the general formula (XI) is preferably slightly. When it is used for a liquid crystal display element having a small driving voltage, the content of the compound represented by the general formula (XI) is preferably slightly. Further, when it is used for a liquid crystal display element used in a low-temperature environment, the content of the compound represented by the formula (XI) is preferably slightly less. When it is used for a liquid crystal composition of a liquid crystal display element having a high reaction rate, the content of the compound represented by the general formula (XI) is preferably slightly less.

Further, the compound represented by the formula (XI) used in the liquid crystal composition of the present invention is preferably a compound represented by the formula (XI-1). (In the formula, R ¹¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but solubility in a low temperature, transition temperature, electron reliability, birefringence, and the like can be considered, and the plural represented by the above formula (XI-1) is suitably combined for each embodiment. Compound. For example, in one embodiment of the present invention, one type is used, and in another embodiment, two types are used, and in still another embodiment, three types or more are combined.

The content of the compound represented by the formula (XI-1) is preferably a solubility at a low temperature, a transition temperature, an electron reliability, etc., and is preferably 1% by mass or more based on the total mass of the liquid crystal composition of the present invention. quality% In the following, it is more preferably 3% by mass or more and 20% by mass or less, and particularly preferably 4% by mass or more and 20% by mass or less, particularly preferably 6% by mass or more and 15% by mass or less, and particularly preferably 9% by mass or more and 12% by mass or less.

Further, the compound represented by the formula (XI-1) used in the liquid crystal composition of the present invention is specifically preferably a compound represented by the formula (45.1) to the formula (45.4), and it is preferred to contain a formula ( 45.2) The compound represented by the formula (45.4) is more preferably a compound represented by the formula (45.2).

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (45.2) is preferably a solubility at a low temperature, a transition temperature, an electron reliability, etc., and is preferably based on the total mass of the liquid crystal composition of the present invention. It is 1% by mass or more and 25% by mass or less, more preferably 2% by mass or more and 20% by mass or less, and particularly preferably 3% by mass or more and 15% by mass or less, particularly preferably 4% by mass or more and 10% by mass or less, and most preferably 4% by mass or less. The mass% or more is 5% by mass or less.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (45.3) is considered in consideration of solubility at low temperature, transition temperature, and electrons. The reliability and the like are preferably 1% by mass or more and 25% by mass or less, more preferably 3% by mass or more and 20% by mass or less, and particularly preferably 3% by mass or more and 15% by mass or less based on the total mass of the liquid crystal composition of the present invention. Hereinafter, it is particularly preferably from 3% by mass to 10% by mass.

In the range of 3% by mass or more and 6% by mass or less, 7% by mass or more and 10% by mass or less, 5% by mass or more and 8% by mass or less, and 6% by mass or more and 7% by mass or less.

In the liquid crystal composition of the present invention, the content of the compound represented by the formula (45.4) is preferably a solubility at a low temperature, a transition temperature, an electron reliability, etc., and is preferably based on the total mass of the liquid crystal composition of the present invention. It is 1% by mass or more and 25% by mass or less, more preferably 2% by mass or more and 20% by mass or less, and particularly preferably 3% by mass or more and 15% by mass or less, particularly preferably 3% by mass or more and 10% by mass or less, and most preferably 3 The mass% or more is 5% by mass or less.

Further, the compound represented by the formula (XI) used in the liquid crystal composition of the present invention is preferably a compound represented by the formula (XI-2). (In the formula, R ¹¹⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but solubility in a low temperature, a transition temperature, an electron reliability, a birefringence, and the like can be considered, and the plural represented by the above formula (XI-2) is suitably combined for each embodiment. Compound. For example, in one embodiment of the present invention, there are one type, and in another embodiment, two types, and in still another embodiment, three types. Combination above the class.

The content of the compound represented by the formula (XI-2) is preferably a solubility at a low temperature, a transition temperature, an electron reliability, etc., and is preferably 1% by mass or more based on the total mass of the liquid crystal composition of the present invention. The mass% or less is more preferably 3% by mass or more and 20% by mass or less, more preferably 4% by mass or more and 20% by mass or less, particularly preferably 6% by mass or more and 15% by mass or less, particularly preferably 9% by mass or more and 12% by mass or less. the following.

Further, the compound represented by the formula (XI-2) used in the liquid crystal composition of the present invention is specifically preferably a compound represented by the formula (45.11) to the formula (45.14), and it is preferred to contain a formula ( 45.12) The compound of the formula (45.14) is more preferably a compound represented by the formula (45.12).

Further, the compound represented by the formula (X) is preferably a compound selected from the group represented by the formula (XII). (wherein, X ¹²¹ to X ¹²⁶ each independently represent a fluorine atom or a hydrogen atom, and R ¹²⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkyl group having 1 to 4 carbon atoms; Oxy group, Y ¹² represents a fluorine atom or -OCF ₃ ).

The compound which can be combined is not particularly limited, but one of the plural compounds represented by the above formula (XII) is preferably one in consideration of solubility at low temperature, transition temperature, electron reliability, birefringence and the like. The combination of 3 or more types is more preferably one to four or more types.

Further, the compound represented by the formula (XII) used in the liquid crystal composition of the present invention is preferably a compound represented by the formula (XII-1). (wherein R ¹²⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but it is preferably one of the plural compounds represented by the above formula (XII-1) in consideration of solubility at low temperature, transition temperature, electron reliability, birefringence and the like. The combination is more than two types, and more preferably one to three or more types.

The content of the compound represented by the formula (XII-1) is preferably a solubility at a low temperature, a transition temperature, an electron reliability, and the like, and is preferably 1% by mass or more based on the total mass of the liquid crystal composition of the present invention. The mass% or less is more preferably 2% by mass or more and 10% by mass or less, and particularly preferably 3% by mass or less. The above is 8 mass% or less, and particularly preferably 4 mass% or more and 6 mass% or less.

Further, the compound represented by the formula (XII-1) used in the liquid crystal composition of the present invention is specifically preferably a compound represented by the formula (46.1) to the formula (46.4), and it is preferred to contain a formula ( 46.2) to a compound of the formula (46.4).

Further, the compound represented by the formula (XII) is preferably a compound represented by the formula (XII-2). (wherein R ¹²⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The compound which can be combined is not particularly limited, but in view of solubility at low temperature, transition temperature, electron reliability, birefringence and the like, 1 of the compound of the above formula (XII-2) is preferred. Kind to The combination of two or more types is more preferably one to three or more types.

The content of the compound represented by the formula (XII-2) is preferably a solubility at a low temperature, a transition temperature, an electron reliability, and the like, and is preferably 1% by mass or more based on the total mass of the liquid crystal composition of the present invention. The mass% or less is more preferably 3% by mass or more and 20% by mass or less, more preferably 4% by mass or more and 17% by mass or less, particularly preferably 6% by mass or more and 15% by mass or less, and particularly preferably 9% by mass or more and 13% by mass or less. the following.

Further, the compound represented by the formula (XII-2) used in the liquid crystal composition of the present invention is specifically preferably a compound represented by the formula (47.1) to the formula (47.4), and preferably contains a formula ( 47.2) to a compound of the formula (47.4).

Further, the compound represented by the formula (M) is preferably a compound selected from the group of compounds represented by the formula (XIII). (wherein, X ¹³¹ to X ¹³⁵ each independently represent a fluorine atom or a hydrogen atom, and R ¹³⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkane having 1 to 4 carbon atoms; Oxy group, Y ¹³ represents a fluorine atom or -OCF ₃ ).

The type of the compound which can be combined is not particularly limited, but it is preferably one type to two types of the compound represented by the above formula (XIII), more preferably one to three types, and particularly preferably Contains 1 to 4 species.

The content of the compound represented by the formula (XIII) is based on properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence, and has an upper limit and a lower limit in each embodiment.

For example, in one embodiment of the present invention, the content of the compound is 2 to 30% by mass based on the total mass of the liquid crystal composition of the present invention, and in another embodiment, the content of the compound is 4 to 30% by mass. In still another embodiment, the content of the compound is 5 to 30% by mass, and in still another embodiment, the content of the compound is 7 to 30% by mass, and in yet another embodiment, The content of the compound is 9 to 30% by mass, and in still another embodiment, the content of the compound is 11 to 30% by mass, and in still another embodiment, the content of the compound is 13 to 30% by mass. . In still another embodiment, the content of the compound is from 14 to 30% by mass. In still another embodiment, the content of the compound is from 16 to 30% by mass. In still another embodiment, the content of the compound is from 20 to 30% by mass.

Further, for example, in one embodiment of the present invention, the content of the compound is 2 to 30% by mass based on the total mass, and in another embodiment, the content of the compound is 2 to 25% by mass. In one embodiment, the content of the compound is 2 to 20% by mass, and in still another embodiment, the content of the compound is 2 to 15% by mass. In still another embodiment, the content of the compound is In another embodiment, the content of the compound is 2 to 5% by mass.

When the liquid crystal composition of the present invention is used for a liquid crystal display device having a small liquid crystal layer gap, the content of the compound represented by the formula (XIII) is preferably slightly. When it is used for a liquid crystal display element having a small driving voltage, the content of the compound represented by the formula (XIII) is preferably slightly more. Further, when it is used for a liquid crystal display element used in a low-temperature environment, the content of the compound represented by the formula (XIII) is preferably slightly less. When it is used for a liquid crystal composition of a liquid crystal display element having a high reaction rate, the content of the compound represented by the formula (XIII) is preferably slightly less.

Further, the compound represented by the formula (XIII) is preferably a compound represented by the formula (XIII-1). (In the formula, R ¹³⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The total mass of the liquid crystal composition of the present invention is preferably 1% by mass or more and 25% by mass or less based on the formula (XIII-1). The compound is preferably contained in an amount of 3% by mass or more and 25% by mass or less, more preferably 5% by mass or more and 20% by mass or less, and particularly preferably 10% by mass or more and 15% by mass or less.

Further, the compound represented by the formula (XIII-1) is preferably a compound represented by the formula (48.1) to the formula (48.4), and a compound represented by the formula (48.2) is preferred.

Further, the compound represented by the formula (XIII) is preferably a compound represented by the formula (XIII-2). (In the formula, R ¹³⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The kind of the compound which can be combined is not particularly limited, but is preferably a compound containing the plural compound represented by the above formula (XIII-2). One type to two or more types.

The compound represented by the formula (XIII-2) is preferably contained in an amount of 5% by mass or more and 25% by mass or less, and more preferably 6% by mass or more and 25% by mass or less, based on the total mass of the liquid crystal composition of the present invention. It is particularly preferably contained in an amount of 8 mass% or more and 20 mass% or less, and particularly preferably 10% by mass or more and 15% by mass or less.

Further, the compound represented by the formula (XIII-2) is preferably a compound represented by the formula (49.1) to the formula (49.4), and preferably a compound represented by the formula (49.1) or the formula (49.2).

Further, the compound represented by the formula (XIII) is preferably a compound represented by the formula (XIII-3). (In the formula, R ¹³⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The type of the compound which can be combined is not particularly limited, but it is preferably one to two kinds of the compound of the plural compound represented by the above formula (XIII-3).

The compound represented by the formula (XIII-3) is preferably contained in an amount of 2% by mass or more and 20% by mass or less, more preferably 4% by mass or more and 20% by mass or less, based on the total mass of the liquid crystal composition of the present invention. More preferably, it is 9% by mass or more and 17% by mass or less, and particularly preferably 11% by mass or more and 14% by mass or less.

Further, the compound represented by the formula (XIII-3) is preferably a compound represented by the formula (50.1) to the formula (50.4), and preferably a compound represented by the formula (50.1) or the formula (50.2).

Further, the compound represented by the formula (M) is preferably a compound selected from the group of compounds represented by the formula (XIV). However, except for the compound represented by the general formula (i), (wherein R ¹⁴⁰ represents an alkyl group having 1 to 7 carbon atoms, an alkenyl group having 2 to 7 carbon atoms or an alkoxy group having 1 to 7 carbon atoms; and X ¹⁴¹ to X ¹⁴⁴ each independently represent a fluorine atom or A hydrogen atom, Y ¹⁴ represents a fluorine atom, a chlorine atom or -OCF ₃ , and Q ¹⁴ represents a single bond, -COO- or -CF ₂ O-, and m ¹⁴ is 0 or 1).

The type of the compound which can be combined is not limited, but the solubility at a low temperature, the transition temperature, the electron reliability, the birefringence, and the like are considered, and a compound of the plural formula represented by the above formula (XIV) is suitably combined for each embodiment. For example, in one embodiment of the present invention, it is one type. Furthermore, in another embodiment of the present invention, there are two types. Alternatively, in still another embodiment of the present invention, there are three types. Further, in still another embodiment of the present invention, there are four types. Alternatively, in still another embodiment of the present invention, there are five types. Alternatively, in still another embodiment of the present invention, it is six or more types.

The content of the compound represented by the formula (XIV) is in consideration of properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence, and has an upper limit and a lower limit in each embodiment.

For example, in one embodiment of the present invention, the content of the compound is from 3 to 40% by mass based on the total mass of the liquid crystal composition of the present invention, and in another embodiment, the content of the compound is from 7 to 40% by mass. In still another embodiment, the content of the compound is 8 to 40% by mass, and in still another embodiment, the compound is The content is 11 to 40% by mass, and in still another embodiment, the content of the compound is 12 to 40% by mass, and in still another embodiment, the content of the compound is 16 to 40% by mass. In still another embodiment, the content of the compound is from 18 to 40% by mass. In still another embodiment, the content of the compound is from 19 to 40% by mass. In still another embodiment, the content of the compound is from 22 to 40% by mass. In still another embodiment, the content of the compound is from 25 to 40% by mass.

Further, for example, in one embodiment of the present invention, the content of the compound is from 3 to 40% by mass based on the total mass, and in another embodiment, the content of the compound is from 3 to 35% by mass. In one embodiment, the content of the compound is 3 to 30% by mass, and in still another embodiment, the content of the compound is 3 to 25% by mass. In still another embodiment, the content of the compound is In another embodiment, the content of the compound is from 3 to 15% by mass.

When the liquid crystal composition of the present invention is used for a liquid crystal display element having a small driving voltage, the content of the compound represented by the general formula (XIV) is preferably slightly increased. Further, in the case of a liquid crystal composition used for a liquid crystal display element having a high reaction rate, the content of the compound represented by the formula (XIV) is preferably slightly less.

Further, the compound represented by the formula (XIV) is preferably a compound represented by the formula (XIV-1). (wherein R ¹⁴⁰ represents an alkyl group having 1 to 7 carbon atoms, an alkenyl group having 2 to 7 carbon atoms or an alkoxy group having 1 to 7 carbon atoms; and Y ¹⁴ represents a fluorine atom, a chlorine atom or -OCF ₃ ).

The type of the compound which can be combined is not limited, but it is preferably one of the plural compounds represented by the above formula (XIV-1) in consideration of solubility at low temperature, transition temperature, electron reliability, birefringence and the like. Kind to 3 kinds of combinations.

Further, the compound represented by the formula (XIV-1) is preferably a compound represented by the formula (XIV-1-1). (In the formula, R ¹⁴⁰ represents an alkyl group having 1 to 7 carbon atoms, an alkenyl group having 2 to 7 carbon atoms or an alkoxy group having 1 to 7 carbon atoms).

The content of the compound represented by the formula (XIV-1) is preferably 2% by mass or more, more preferably 4% by mass or more, and particularly preferably 7% by mass or more, based on the total mass of the liquid crystal composition of the present invention. It is preferably 10% by mass or more, and particularly preferably 18% by mass or more. Further, considering the solubility at low temperature, the transition temperature, the electron reliability, and the like, the maximum ratio is preferably limited to 30% by mass or less, more preferably 27% by mass or less, still more preferably 24% by mass or less, and particularly preferably less than 21%. quality%.

Further, the compound represented by the formula (XIV-1-1) is specifically preferably a compound represented by the formula (51.1) to the formula (51.4), and more preferably a compound represented by the formula (51.1).

Further, the compound represented by the formula (XIV-1) is preferably a compound represented by the formula (XIV-1-2). (In the formula, R ¹⁴⁰ represents an alkyl group having 1 to 7 carbon atoms, an alkenyl group having 2 to 7 carbon atoms or an alkoxy group having 1 to 7 carbon atoms).

The content of the compound represented by the formula (XIV-1-2) is considered to be solubility at a low temperature, a transition temperature, an electron reliability, etc., and is preferably 1% by mass based on the total mass of the liquid crystal composition of the present invention. The amount is 15% by mass or less, more preferably 3% by mass or more and 13% by mass or less, and particularly preferably 5% by mass or more and 11% by mass or less, and particularly preferably 7% by mass or more and 9% by mass or less.

Further, the compound represented by the formula (XIV-1-2) is specifically preferably a compound represented by the formula (52.1) to the formula (52.4), and preferably a compound represented by the formula (52.4).

Further, the compound represented by the formula (XIV) is preferably a compound represented by the formula (XIV-2). However, except for the compound represented by the general formula (i), (wherein R ¹⁴⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms; and X ¹⁴¹ to X ¹⁴⁴ each independently represent a fluorine atom or A hydrogen atom, Y ¹⁴ represents a fluorine atom, a chlorine atom or -OCF ₃ ).

The type of the compound which can be combined is not limited, but solubility in a low temperature, a transition temperature, an electron reliability, a birefringence, etc. are considered, and the plural represented by the above formula (XIV-2) is suitably combined for each embodiment. Compound. For example, in one embodiment of the present invention, it is one type. Furthermore, in another embodiment of the present invention, there are two types. Alternatively, in still another embodiment of the present invention, there are three types. Further, in still another embodiment of the present invention, there are four types. Alternatively, in still another embodiment of the present invention, it is five or more types.

The content of the compound represented by the formula (XIV-2) is in consideration of properties such as solubility at low temperature, transition temperature, electron reliability, and birefringence, and has an upper limit and a lower limit in each embodiment.

For example, in one embodiment of the present invention, the content of the compound is from 3 to 40% by mass based on the total mass of the liquid crystal composition of the present invention, and in another embodiment, the content of the compound is 7 to 40% by mass, in still another embodiment, the content of the compound is 8 to 40% by mass, and in still another embodiment, the content of the compound is 10 to 40% by mass, and yet another In another embodiment, the content of the compound is 11 to 40% by mass, and in still another embodiment, the content of the compound is 12 to 40% by mass, and in still another embodiment, the content of the compound is 18 ~40% by mass. In still another embodiment, the content of the compound is from 19 to 40% by mass. In still another embodiment, the content of the compound is from 21 to 40% by mass. In still another embodiment, the content of the compound is from 22 to 40% by mass.

Further, for example, in one embodiment of the present invention, the content of the compound is from 3 to 40% by mass based on the total mass, and in another embodiment, the content of the compound is from 3 to 35% by mass. In one embodiment, the content of the compound is 3 to 25% by mass, and in still another embodiment, the content of the compound is 3 to 20% by mass. In still another embodiment, the content of the compound is In another embodiment, the content of the compound is from 3 to 10% by mass.

When the liquid crystal composition of the present invention is used for a liquid crystal display element having a small driving voltage, the content of the compound represented by the formula (XIV-2) is preferably slightly more. Further, in the case of a liquid crystal composition used for a liquid crystal display element having a high reaction rate, the content of the compound represented by the formula (XIV-2) is preferably slightly less.

Further, the compound represented by the formula (XIV-2) is preferably a compound represented by the formula (XIV-2-1). (In the formula, R ¹⁴⁰ represents an alkyl group having 1 to 5 carbon atoms, an alkenyl group having 2 to 5 carbon atoms or an alkoxy group having 1 to 4 carbon atoms).

The content of the compound represented by the formula (XIV-2-1) is considered to be solubility at a low temperature, a transition temperature, an electron reliability, etc., and is preferably 1% by mass based on the total mass of the liquid crystal composition of the present invention. The amount is 15% by mass or less, more preferably 3% by mass or more and 13% by mass or less, and particularly preferably 5% by mass or more and 11% by mass or less, and particularly preferably 7% by mass or more and 9% by mass or less.

Further, the compound represented by the formula (XIV-2-1) is specifically preferably a compound represented by the formula (53.1) to the formula (53.4), and preferably a compound represented by the formula (53.4).

The compound used in the invention of the present invention does not have a peracid (-CO-OO-) structure in the molecule. Moreover, when importance is attached to the reliability and long-term stability of the liquid crystal composition, it is preferred not to use a compound having a carbonyl group. Further, when importance is attached to the stability of UV irradiation, it is preferred not to use a compound substituted with a chlorine atom. It is also preferred that only the intramolecular ring structure is a 6-membered ring compound.

The liquid crystal composition of the present invention is preferably a compound which does not contain a structure in which oxygen atoms having a peracid (-CO-OO-) structure or the like are bonded to each other in the molecule.

Pay attention to the reliability and long-term stability of liquid crystal compositions The content of the compound having a carbonyl group is preferably 5% by mass or less, more preferably 3% by mass or less, even more preferably 1% by mass or less, based on the total mass of the above-mentioned composition, and is preferably substantially not contained.

When the stability of the UV irradiation is emphasized, the content of the chlorine atom-substituted compound is preferably 15% by mass or less, more preferably 10% by mass or less, even more preferably 5% by mass or less, based on the total mass of the composition. Jia is not actually included.

Preferably, the content of the compound having a ring structure of 6 in the molecule is increased, and the content of the compound having a ring structure of 6 members in the molecule is preferably 80% by mass or more, more preferably the total mass of the composition. It is 90% by mass or more, and particularly preferably 95% by mass or more. It is preferable to form a liquid crystal composition only by a compound having a ring structure of substantially 6 in the molecular structure.

In order to suppress deterioration of the liquid crystal composition due to oxidation, it is preferred to reduce the content of the compound having a cyclohexene group as a ring structure, and the content of the compound having a cyclohexene group is preferably relative to the total mass of the above composition. 10% by mass or less, more preferably 5% by mass or less, and particularly preferably substantially not contained.

When attention is paid to the improvement of viscosity and the improvement of Tni, it is preferred to reduce the content of a compound having a 2-methylbenzene-1,4-diyl group in which a hydrogen atom can be substituted into a halogen, and the molecule has a hydrogen atom. The content of the compound of the 2-methylbenzene-1,4-diyl group which may be substituted with a halogen is preferably 10% by mass or less, more preferably 5% by mass or less, based on the total mass of the above-mentioned composition. Jia is not actually included.

When the compound contained in the composition of the first embodiment of the present invention has an alkenyl group as a side chain, it is preferred that the compound is an alkenyl bond. When the cyclohexane is formed, the alkenyl group has 2 to 5 carbon atoms, preferably when the alkenyl group is bonded to benzene, the alkenyl group has 4 to 5 carbon atoms, preferably the aforementioned alkenyl group. The unsaturated bond is not directly bonded to benzene.

In the liquid crystal display device of the present invention, a polymerizable compound may be contained in order to produce a liquid crystal display element such as a PS mode, a lateral electric field type PSA mode or a lateral electric field type PSVA mode. The polymerizable compound which can be used is a photopolymerizable monomer which is polymerized by an energy ray such as light, and the structure is, for example, a six-membered ring having a biphenyl derivative or a biphenyl derivative. A polymerizable compound or the like of a liquid crystal skeleton which is connected in plural. More specifically, a difunctional monomer represented by the formula (XX) is preferred, (wherein, X ²⁰¹ and X ²⁰² each independently represent a hydrogen atom or a methyl group, and Sp ²⁰¹ and Sp ²⁰² each independently represent a single bond, an alkylene group having 1 to 8 carbon atoms or -O-(CH ₂ ) _s - (wherein s represents an integer from 2 to 7, the oxygen atom is bonded to the aromatic ring), and Z ²⁰¹ represents -OCH ₂ -, -CH ₂ O-, -COO-, -OCO-, -CF ₂ O- , -OCF ₂ -, -CH ₂ CH ₂ -, -CF ₂ CF ₂ -, -CH=CH-COO-, -CH=CH-OCO-, -COO-CH=CH-, -OCO-CH=CH -, -COO-CH ₂ CH ₂ -, -OCO-CH ₂ CH ₂ -, -CH ₂ CH ₂ -COO-, -CH ₂ CH ₂ -OCO-, -COO-CH ₂ -, -OCO-CH ₂ -, -CH ₂ -COO-, -CH ₂ -OCO-, -CY ¹ =CY ² - (wherein Y ¹ and Y ² each independently represent a fluorine atom or a hydrogen atom), -C≡C- or a single a bond, M ²⁰¹ represents a 1,4-phenylene group, a trans-1,4-cyclohexylene group or a single bond, and all of the 1,4-phenylene groups in the formula may be substituted by a fluorine atom. .

X ²⁰¹ and X ^{202 are} preferably a diacrylate derivative each having a hydrogen atom, and a dimethacrylate derivative each having a methyl group, and it is also preferred that one of them represents a hydrogen atom, and the other One represents a compound of a methyl group. The polymerization rate of these compounds is the fastest in the diacrylate derivative, the dimethacrylate derivative is slow, and the asymmetric compound is in the middle thereof, and a preferred aspect can be used according to the use thereof. Among the PSA display elements, dimethacrylate derivatives are particularly preferred.

Sp ²⁰¹ and Sp ²⁰² each independently represent a single bond, an alkylene group having 1 to 8 carbon atoms or -O-(CH ₂ ) _s -, but in the PSA display element, at least one is preferably a single bond. Preferred are all compounds which represent a single bond, or one of which is a single bond and the other represents an alkylene group having 1 to 8 carbon atoms or -O-(CH ₂ ) _s -. In this case, an alkyl group of 1 to 4 is preferable, and s is preferably 1 to 4.

Z ^{201 is} preferably -OCH ₂ -, -CH ₂ O-, -COO-, -OCO-, -CF ₂ O-, -OCF ₂ -, -CH ₂ CH ₂ -, -CF ₂ CF ₂ - or The key is more preferably -COO-, -OCO- or a single bond, and particularly preferably a single bond.

M ²⁰¹ represents a 1,4-phenylene group, a trans-1,4-cyclohexylene group or a single bond in which an arbitrary hydrogen atom may be substituted by a fluorine atom, but is preferably a 1,4-phenylene group or a single bond. When C represents a ring structure other than a single bond, Z ^{201 is} also preferably a linking group other than a single bond, and when M ²⁰¹ is a single bond, Z ^{201 is} preferably a single bond.

Based on these points, in the general formula (XX), the ring structure between Sp ²⁰¹ and Sp ²⁰² is specifically preferably the structure described below.

In the formula (XX), when M ²⁰¹ represents a single bond and the ring structure is formed by two rings, it preferably represents the following formula (XXa-1) to formula (XXa-5), more preferably a formula (XXa). -1) to the formula (XXa-3), particularly preferably the expression (XXa-1), (wherein both ends are bonded to Sp ²⁰¹ or Sp ²⁰² ).

The polymerizable compound containing these skeletons is most suitable for a PSA liquid crystal display device because of the alignment adjustment force after polymerization, and a good alignment state is obtained. Therefore, display unevenness is suppressed or does not occur at all.

According to the above, the polymerizable monomer is particularly preferably of the formula (XX-1) to the formula (XX-4), and the most preferred formula (XX-2), (wherein, Sp ²⁰ represents an alkylene group having 2 to 5 carbon atoms).

When a monomer is added to the liquid crystal composition of the present invention, polymerization is carried out even when the polymerization initiator is not present, but a polymerization initiator may be contained in order to promote polymerization. Examples of the polymerization initiator include benzoin ethers, diphenylketones, acetophenones, benzyl ketals, and mercaptophosphine oxides.

The liquid crystal composition of the present invention may further contain a compound represented by the formula (Q). (wherein R ^Q represents a linear alkyl group or a branched alkyl group having 1 to 22 carbon atoms, and one or two or more CH ₂ groups in the alkyl group are not directly adjacent to each other in the oxygen atom; Substituted by -O-, -CH=CH-, -CO-, -OCO-, -COO-, -C≡C-, -CF ₂ O-, -OCF ₂ -, M ^Q represents trans-1,4 - a cyclohexyl group, a 1,4-phenylene group or a single bond).

R ^Q represents a linear alkyl group or a branched alkyl group having 1 to 22 carbon atoms, and one or two or more CH ₂ groups in the alkyl group may be -O- in such a manner that the oxygen atoms are not directly adjacent to each other. , -CH=CH-, -CO-, -OCO-, -COO-, -C≡C-, -CF ₂ O-, -OCF ₂ -, preferably a linear alkane having from 1 to 10 carbon atoms a linear alkyl group in which a radical, a linear alkoxy group, a CH ₂ group is substituted with -OCO- or -COO-, a branched alkyl group, a branched alkoxy group, and a CH ₂ group are substituted into -OCO a branched alkyl group of -OR-COO-, more preferably a linear alkyl group having 1 to 20 carbon atoms, a linear alkyl group in which 1 CH ₂ group is substituted with -OCO- or -COO-, a branched alkyl group The group, the branched alkoxy group, and one CH ₂ group are substituted with a branched alkyl group of -OCO- or -COO-. M ^Q represents a trans-1,4-cyclohexylene group, a 1,4-phenylene group or a single bond, preferably a trans-1,4-cyclohexylene group or a 1,4-phenylene group.

More specifically, the compound represented by the formula (Q) is preferably a compound represented by the following formula (Q-a) to formula (Q-d).

In the formula, R ^{Q1 is} preferably a linear alkyl group or a branched alkyl group having 1 to 10 carbon atoms, and R ^{Q2 is} preferably a linear alkyl group or a branched alkyl group having 1 to 20 carbon atoms, and R ^Q3 is more preferred. Preferred is a linear alkyl group having 1 to 8 carbon atoms, a branched alkyl group, a linear alkoxy group or a branched alkoxy group, and L ^{Q is} preferably a linear alkyl group or a branch having 1 to 8 carbon atoms. Chain alkyl. Among the compounds represented by the formula (Qa) to the formula (Qd), a compound represented by the formula (Qc) and the formula (Qd) is more preferred.

In the liquid crystal composition of the present invention, it is preferred to contain one or two kinds of compounds represented by the formula (Q), more preferably one to five, and the content thereof is preferably from 0.001 to 1% by mass. More preferably, it is 0.001 to 0.1% by mass, and particularly preferably 0.001 to 0.05% by mass.

<Liquid crystal display element>

The liquid crystal composition containing a polymerizable compound of the present invention is capable of polymerizing a polymerizable compound contained therein by ultraviolet irradiation to impart a liquid crystal alignment ability, and is used for liquid crystal which controls the amount of light transmitted by the birefringence of the liquid crystal composition. Display component. For liquid crystal display elements, suitable for ECB-LCD, VA-LCD, FFS-LCD, AM-LCD (active matrix liquid crystal display device), TN (nematic liquid crystal display device), STN-LCD (super twisted nematic liquid crystal display) The component), OCB-LCD and IPS-LCD (transverse electric field switching liquid crystal display element) are particularly suitable for AM-LCD, and can be used for a transmissive or reflective liquid crystal display element.

The two substrates of the liquid crystal cell used in the liquid crystal display element can be made of a transparent material such as glass or plastic, and one of them can also be made of an opaque material such as tantalum. The transparent substrate having a transparent electrode layer can be obtained, for example, by sputtering indium tin oxide (ITO) on a transparent substrate such as a glass plate.

The color filter can be produced, for example, by a pigment dispersion method, a printing method, an electrodeposition method, a dyeing method, or the like. An example of a method for producing a color filter by a pigment dispersion method is to apply a curable coloring composition for a color filter to a transparent substrate, apply a patterning treatment, and then heat or lightly irradiate. Harden. By red, green, Each of the three blue colors performs this step to form a pixel portion for a color filter. Further, a pixel electrode provided with an active element such as a TFT or a thin film diode may be provided on the substrate.

The substrates are opposed to each other such that the transparent electrode layer is inside. In this case, the interval between the substrates can also be adjusted via the spacer. In this case, it is preferred to adjust so that the thickness of the obtained light control layer is 1 to 100 μm. More preferably, it is 1.5 to 10 μm. When a polarizing plate is used, it is preferable to adjust the product of the refractive index anisotropy Δn of the liquid crystal and the cell thickness d in such a manner that the contrast is maximized. Moreover, when there are two polarizing plates, the polarizing axes of the respective polarizing plates can be adjusted, and the viewing angle or the contrast can be adjusted in a good manner. Further, in order to expand the viewing angle, a retardation film can also be used. Examples of the spacer include a columnar spacer formed of glass particles, plastic particles, alumina particles, a photoresist material, or the like. Then, a sealant such as an epoxy thermosetting composition is screen-printed on the substrate in the form of a liquid crystal injection port, and the substrates are bonded to each other and heated to thermally cure the sealant.

A method of sandwiching a liquid crystal composition containing a polymerizable compound between two substrates can be carried out by a usual vacuum injection method, ODF method or the like. However, in the vacuum injection method, although the dropping trace does not occur, the problem of residual trace of the injection is more suitable for the display element manufactured by the ODF method in the invention of the present invention. In the liquid crystal display element manufacturing step of the ODF method, an epoxy-based photothermal heat is used as a closed-loop embankment in a sealing agent such as hardenability by using a dispenser on any of the back sheet or the front sheet. After dropping a specified amount of the liquid crystal composition under degassing, the front plate and the back plate are bonded to each other to manufacture a liquid crystal display element. Liquid crystal composition of the present invention The material can be suitably used because the dripping of the liquid crystal composition is carried out in the ODF step.

As a method of polymerizing the polymerizable compound, in order to obtain a good alignment property of the liquid crystal, it is preferred to have a moderate polymerization rate. Therefore, it is preferred to polymerize by direct or alternately or alternately irradiating active energy rays such as ultraviolet rays or electron beams. The method. When using ultraviolet light, a polarized light source or a non-polarized light source can be used. In addition, when the liquid crystal composition containing the polymerizable compound is sandwiched between the two substrates, the substrate on the irradiation surface side must have appropriate transparency to the active energy ray. Further, it is also possible to use a mask to modulate only a specific portion after light irradiation, and to change the alignment state of the unpolymerized portion by changing conditions such as an electric field, a magnetic field, or a temperature, and then irradiate the active energy ray so that the active energy ray is irradiated. The means of aggregation. In particular, in the case of ultraviolet light exposure, it is preferred to perform ultraviolet exposure while applying an alternating electric field to the liquid crystal composition containing the polymerizable compound. The applied alternating electric field is preferably an alternating current having a frequency of 10 Hz to 10 kHz, more preferably a frequency of 60 Hz to 10 kHz, and the voltage is selected depending on the desired pretilt angle of the liquid crystal display element. That is, the pretilt angle of the liquid crystal display element can be controlled by the applied voltage. In the liquid crystal display device of the transverse electric field type MVA mode, it is preferable to control the pretilt angle from 80 to 89.9 degrees from the viewpoint of alignment stability and contrast.

The temperature at the time of irradiation is preferably within a temperature range in which the liquid crystal state of the liquid crystal composition of the present invention is maintained. It is preferred to carry out the polymerization at a temperature close to room temperature, that is, typically at a temperature of from 15 to 35 °C. As the lamp for generating ultraviolet rays, a metal halide lamp, a high pressure mercury lamp, an ultrahigh pressure mercury lamp, or the like can be used. Further, as the wavelength of the ultraviolet ray to be irradiated, it is preferred to irradiate the ultraviolet ray in the wavelength range of the absorption wavelength range of the non-liquid crystal composition, and it is preferable to use the ultraviolet ray to cut off the ultraviolet ray if necessary. The intensity of the ultraviolet ray to be irradiated is preferably from 0.1 mW/cm ² to 100 W/cm ² , more preferably from 2 mW/cm ² to 50 W/cm ² . The energy of the ultraviolet ray to be irradiated can be suitably adjusted, but is preferably from 10 mJ/cm ² to 500 J/cm ² , more preferably from 100 mJ/cm ² to 200 J/cm ² . When the ultraviolet ray is irradiated, the intensity can also be changed. The time for irradiating the ultraviolet rays is appropriately selected depending on the intensity of the ultraviolet rays to be irradiated, but is preferably from 10 seconds to 3600 seconds, more preferably from 10 seconds to 600 seconds.

The liquid crystal display element using the liquid crystal composition of the present invention can be used for coexisting the suppression of rapid reaction and display failure, and is particularly useful for a liquid crystal display element for active matrix driving, and is applicable to VA mode, PSVA mode, PSA mode, IPS ( Transverse electric field switching) mode, FFS (wide viewing angle technology) mode or liquid crystal display element for ECB mode.

Hereinafter, a preferred embodiment of the liquid crystal display device (liquid crystal display) of the present invention will be described in detail with reference to the drawings.

Fig. 1 is a cross-sectional view showing a liquid crystal display device including two substrates facing each other, a sealing material provided between the substrates, and a liquid crystal sealed in a closed region surrounded by the sealing material.

Specifically, a specific aspect of the liquid crystal display device is provided, and the TFT substrate 102 and the pixel electrode 103 are provided on the first substrate 100, and a back sheet of the passivation film 104 and the first alignment film 105 is provided thereon; On the second substrate 200, a black matrix 202, a color filter 203, a flattening film (cover layer) 201, and a transparent electrode 204 are provided, and a second alignment film 205 is provided from above to face the front plate. a sealing material 301 disposed between the substrates; and a liquid enclosed in a closed area surrounded by the sealing material The crystal layer 303 is provided with protrusions (columnar spacers) 302 and 304 on the substrate surface to which the sealing material 301 is in contact.

The material of the first substrate or the second substrate is not particularly limited as long as it is substantially transparent, and glass, ceramics, plastic, or the like can be used. As the plastic substrate, cellulose derivatives such as cellulose, triacetyl cellulose, and diethyl phthalocyanine; polycycloolefin derivatives, polyethylene terephthalate, polyethylene naphthalate, and the like can be used. Polyester; polyolefin such as polypropylene, polyethylene, etc.; polycarbonate, polyvinyl alcohol, polyvinyl chloride, polyvinylidene chloride, polyamide, polyimine, polyamidamine, polyphenylene Ethylene, polyacrylate, polymethyl methacrylate, polyether oxime, polyarylate, inorganic-organic composite materials such as glass fiber-epoxy resin, glass fiber-acrylic resin, and the like.

Further, when a plastic substrate is used, it is preferable to provide a barrier film. The function of the barrier film is to reduce the moisture permeability of the plastic substrate and improve the reliability of the electronic characteristics of the liquid crystal display element. The barrier film is not particularly limited as long as it has high transparency and low water vapor permeability. Generally, an inorganic material such as cerium oxide is used, and vapor deposition or sputtering or chemical vapor deposition (CVD) is used. The film formed.

In the present invention, the same material may be used as the first substrate or the second substrate, and different materials may be used, and are not particularly limited. When a glass substrate is used, a liquid crystal display element excellent in heat resistance and dimensional stability can be produced. Further, in the case of a plastic substrate, it is preferably a method of producing a roll-to-roll method, and is preferably lighter or more flexible. In addition, in order to provide flatness and heat resistance, good results can be obtained by combining a plastic substrate and a glass substrate.

Further, in the embodiment described later, a substrate made of the material of the first substrate 100 or the second substrate 200 is used.

In the back sheet, the TFT layer 102 and the pixel electrode 103 are provided on the first substrate 100. These can be manufactured by the usual array steps. The passivation film 104 and the first alignment film 105 are provided thereon to obtain a back sheet.

The passivation film 104 (also referred to as an inorganic protective film) protects the film of the TFT layer, and a nitride film (SiN _x ), an oxide film (SiO _x ), or the like is usually formed by a chemical vapor deposition (CVD) technique or the like.

Further, the first alignment film 105 has a function of aligning the liquid crystal, and a polymer material such as polyimine is usually used. In the coating liquid, an alignment agent solution containing a polymer material and a solvent is used. Since the alignment film has the possibility of hindering the adhesion to the sealing material, the pattern is applied in the closed region. A printing method such as an offset printing method, a droplet discharge method such as inkjet is used for coating. The coated alignment agent solution is cured by crosslinking after evaporation of the solvent by temporary drying. Then, in order to exhibit the alignment function, alignment processing is performed.

The alignment process is usually performed by a rubbing method. The liquid crystal alignment ability is produced by unidirectional rubbing on a polymer film formed as described above by using a rubbing cloth made of fibers such as ruthenium.

Also, there is also the use of the optical alignment method. The photo-alignment method produces a aligning ability by irradiating a polarized light on an alignment film containing a photoreceptive organic material, and does not cause damage or dust of the substrate due to the rubbing method. As an example of the organic material of the photo-alignment method, there is a material containing a dichroic dye. As a dichroic dye, an alignment-induced or heterogeneous molecule having a Weigert effect due to photodichromaticity can be used. Chemical reaction (eg azophenyl), dimerization reaction (eg cassia sulfhydryl), photocrosslinking reaction (eg diphenyl ketone group) or photodecomposition reaction (eg polyethylenimine group) It is the basis of the photoreaction (hereinafter referred to as photo-alignment group) which is the origin of the liquid crystal alignment ability. The applied alignment agent solution is obtained by evaporating a solvent by temporary drying, and by irradiating light having any deviation (polarization), an alignment film having an alignment ability in an arbitrary direction can be obtained.

The other front plate is provided with a black matrix 202, a color filter 203, a planarizing film 201, a transparent electrode 204, and a second alignment film 205 on the second substrate 200.

The black matrix 202 is produced, for example, by a pigment dispersion method. Specifically, on the second substrate 200 provided with the barrier film 201, a colored resin liquid in which a black colorant for forming a black matrix is uniformly dispersed is applied to form a colored layer. Next, the colored layer is baked to be hardened. The photoresist is coated thereon and pre-baked. After the photoresist is exposed by the mask pattern, development is performed to pattern the colored layer. Then, the photoresist layer is peeled off, and the colored layer is baked to complete the black matrix 202.

Alternatively, a photoresist type pigment dispersion liquid can also be used. At this time, a photoresist type pigment dispersion liquid is applied, and after prebaking, after exposure by a mask pattern, development is performed, and the colored layer is patterned. Then, the photoresist layer is peeled off, and the colored layer is baked to complete the black matrix 202.

The color filter 203 is formed by a pigment dispersion method, an electrodeposition method, a printing method, a dyeing method, or the like. In the case of the pigment dispersion method, a colored resin liquid in which a pigment (for example, red) is uniformly dispersed is applied onto the second substrate 200, and after baking curing, a photoresist is applied thereon to perform prebaking. After the photoresist is exposed by the mask pattern, the image is developed, and the pattern is Chemical. The photoresist layer is then stripped and the (red) color filter 203 is completed by baking. The order of coloring is not particularly limited. Similarly, a green color filter 203 and a blue color filter 203 are formed.

The transparent electrode 204 is provided on the color filter 203 (the overcoat layer (201) for surface flattening is provided on the color filter 203 as needed). The transparent electrode 204 preferably has a high transmittance, and preferably has a small resistance. The transparent electrode 204 is formed of an oxide film of ITO or the like by a sputtering method or the like.

Further, for the purpose of protecting the transparent electrode 204, a passivation film may be provided on the transparent electrode 204.

The second alignment film 205 is the same as the first alignment film 105 described above.

In the above, the above-mentioned back sheet and the front sheet used in the present invention are described in a specific aspect, but are not limited to the specific aspect in the present case, and the liquid crystal display element according to the desired aspect is freely available. change.

The shape of the columnar spacer is not particularly limited, and various shapes such as a polygonal shape such as a circular shape or a quadrangular shape may be used, but it is preferable to consider a misalignment margin during the process. To make the horizontal section a circular or regular polygon. Further, the shape of the protrusion is preferably a truncated cone or a truncated cone.

The material of the columnar spacer is not particularly limited as long as it is an organic solvent or a liquid crystal which is used for the sealing material or the sealing material, but is preferably a synthetic resin from the viewpoint of processing and weight reduction. (curable resin). On the other hand, the aforementioned protrusions can be light-driven The engraving method or the droplet discharge method is provided on the sealing material interface on the first substrate. For this reason, it is preferred to use a photocurable resin suitable for a photolithography method or a droplet discharge method.

As an example, the case where the columnar spacer is obtained by photolithography will be described. Fig. 2 is a view showing a step of exposing a pattern using a columnar spacer formed on a black matrix as a mask pattern.

A resin liquid for forming a columnar spacer (excluding a colorant) is applied onto the transparent electrode 204 of the front plate. Next, the resin layer 402 is baked and hardened. The photoresist is coated thereon and pre-baked. After the photoresist is exposed by the mask pattern 401, development is performed to pattern the resin layer. Then, the photoresist layer is peeled off, and the resin layer is baked to complete the columnar spacer (302, 0304 in Fig. 1).

The position at which the column spacers are formed can be positioned at a desired position by a mask pattern. Therefore, both the closed region of the liquid crystal display element and the outside of the closed region (the sealing material coating portion) can be simultaneously formed. Further, it is preferable to form a columnar spacer so as to be located above the black matrix so as not to lower the quality of the closed region. The columnar spacers thus produced by photolithography are referred to as cylindrical spacers or photo spacers.

The material of the spacer is a mixture of a negative water-soluble resin such as a PVA-stilbazo photosensitive resin or a polyfunctional acrylic monomer, an acrylic copolymer, a triazole-based initiator, or the like. Alternatively, there is a method of using a color resin in which a coloring agent is dispersed in a polyimide resin. In the present invention, it is not particularly limited, and a spacer can be obtained from a known material in accordance with the liquid crystal to be used or the compatibility with the sealing material.

In this manner, after the columnar spacer is provided on the surface of the front plate which is the closed region, a sealing material (301 in FIG. 1) is applied to the sealing material contact surface of the back plate.

The material of the sealing material is not particularly limited, and a curable resin composition in which a polymerization initiator is added to an epoxy-based or acrylic-based photocurable, thermosetting, or photocurable resin can be used. Further, in order to control moisture permeability, elastic modulus, viscosity, and the like, a filler composed of an inorganic substance or an organic substance may be added. The shape of these fillers is not particularly limited and may be spherical, fibrous, amorphous or the like. Further, in order to favorably control the gap of the liquid crystal layer, a spherical or fibrous slit material having a monodisperse diameter is mixed, or in order to further strengthen the adhesion to the substrate, a fibrous substance which is easily entangled with the protrusion on the substrate may be mixed. The diameter of the fibrous material used at this time is preferably about 1/5 to 1/10 of the gap of the liquid crystal layer, and the length of the fibrous material is preferably shorter than the width of the seal coating.

In addition, the material of the fibrous material is not particularly limited as long as it has a predetermined shape, and synthetic fibers such as cellulose, polyamide or polyester, or inorganic materials such as glass or carbon can be suitably selected.

As a method of applying the sealing material, there is a printing method or a dispensing method, but it is preferable to use a dispensing method in which the amount of the sealing material used is small. The coating position of the sealing material is usually on a black matrix in order not to adversely affect the enclosed area. In order to form the liquid crystal dropping region of the next step (in such a manner that the liquid crystal does not leak), the sealing material coating shape is a closed loop shape.

The liquid crystal was dropped on the closed-loop shape (closed region) of the front plate coated with the aforementioned sealing material. A dispenser is usually used. The amount of liquid crystal dropped is consistent with the volume of the liquid crystal cell, substantially the height of the column spacer The same amount of volume multiplied by the sealed coated area. However, in order to optimize liquid crystal leakage or display characteristics in the cell bonding step, the amount of liquid crystal dropped may be appropriately adjusted, and the liquid crystal dropping position may be dispersed.

Next, the sealing material is applied, and the back sheet is bonded to the front plate on which the liquid crystal has been dropped. Specifically, the front plate and the back plate are adsorbed by a stage having a mechanism for adsorbing the substrate such as an electrostatic chuck, and the second alignment film of the front plate faces the first alignment film of the back plate, and is disposed on the sealing member and the other side. The position (distance) where the substrates do not meet. In this state, the internal pressure is reduced. After the completion of the pressure reduction, the position of the two substrates (alignment operation) was adjusted while confirming the bonding position of the front plate and the back plate. If the adjustment of the bonding position is completed, the substrate is brought close to the position where the sealing material on the front plate is in contact with the backing plate. In this state, the inert gas is filled in the system, and the pressure is returned to the normal pressure while gradually opening the pressure. At this time, the front plate and the back plate are bonded together by atmospheric pressure, and a liquid crystal layer gap is formed at a height position of the columnar spacer. In this state, the sealing material is irradiated with ultraviolet rays to cure the sealing material to form a liquid crystal cell. Then, a heating step is applied as appropriate to promote hardening of the sealing material. In order to enhance the adhesion of the sealing material or to improve the reliability of the electronic properties, a heating step is applied.

[Examples]

The invention is illustrated in more detail below by the examples, but the invention is not limited by the examples. Moreover, "%" in the compositions of the following examples and comparative examples means "% by mass".

In the examples, the measured characteristics are as follows.

Tni: nematic phase-isotropic liquid phase transition temperature (°C)

Δn: refractive index anisotropy at 295 K (alias: birefringence)

△ ε: dielectric anisotropy at 295K

η: viscosity at 295K (mPa‧s)

Γ1: Rotational viscosity at 295K (mPa‧s)

Initial voltage holding ratio (initial VHR): Voltage holding ratio at 50 ° C at a frequency of 60 Hz and a voltage of 4 V (%)

Voltage holding ratio after heating (VHR after heating): Voltage holding ratio (%) measured under the same conditions as the initial VHR after maintaining for 1 hour in an environment of 150 ° C

<Imprint evaluation>

The imprint evaluation of the liquid crystal display element is performed by displaying the predetermined fixed pattern for 1440 hours in the display area, and when the full-screen uniform display is performed, the degree of the residual image of the fixed pattern is visually recognized by the following four levels.

◎: no afterimage

○: There are very few afterimages, but they are also tolerable.

△: There is an afterimage, which is unacceptable

×: There is an afterimage, quite inferior

<Evaluation of Volatile (Contamination of Manufacturing Equipment)>

The volatility evaluation of the liquid crystal material was carried out by observing the operation state of the vacuum stirring defoaming mixer while illuminating by a stroboscope, and visually observing the foaming of the liquid crystal material. Specifically, the capacity of the vacuum container for dedicated off 0.5L stirred mixer of the bubble in the liquid crystal composition was added 0.15kg, degassed under 4kPa, the revolution speed at 15S ^-1, the rotation speed of operation of the vacuum to 7.5S ^-1 The agitating defoaming mixer was carried out by the following four evaluations by the time until the start of foaming.

◎: It takes 3 minutes or more before foaming. The possibility of contamination of the device caused by volatilization is low.

○: 1 minute or more and less than 3 minutes before foaming. There are concerns about slight device contamination caused by volatilization.

△: 30 seconds or more and less than 1 minute before foaming. Device contamination caused by volatilization.

×: Within 30 seconds before foaming. There are concerns about the pollution of major equipment made by volatilization.

<Evaluation of process suitability>

The process suitability is based on the ODF process. The fixed-volume metering pump is used to drop the liquid crystal at 40pL every 100 times, and the following four levels are used to evaluate the following "0~200 times, 201~400 times, 401~600". The change in the amount of liquid crystal dropped by 200 times each time, ‧ ‧ ‧ 990 801 ~ 100,000 times

◎: The change is extremely small (the liquid crystal display element can be stably manufactured)

○: There is a slight change, but it is also tolerable.

△: There is a change, which is unacceptable (the yield is deteriorated due to the occurrence of spots)

×: There is a change, which is quite inferior (liquid crystal leakage or vacuum bubble occurs)

<Evaluation of Solubility at Low Temperature>

The solubility evaluation at low temperature was carried out by weighing 0.5 g of a liquid crystal composition in a 1 mL vial after modulating the liquid crystal composition, and in the temperature-controlled test tank, the following was regarded as one cycle "-20 ° C ( Hold for 1 hour) → temperature rise (0.2 ° C / min) → 0 ° C (for 1 hour) → temperature increase (0.2 ° C / min )→20°C (for 1 hour)→cooling (-0.2°C/min)→0°C (for 1 hour)→cooling (-0.2°C/min)→-20°C”, continuously give temperature change, visual observation The occurrence of precipitates from the liquid crystal composition was evaluated in the following four grades.

◎: No precipitate was observed for 600 hours or more.

○: No precipitate was observed for 300 hours or longer.

△: Precipitates were observed within 150 hours.

×: Precipitates were observed within 75 hours.

[Example 1 and Comparative Examples 1 to 2]

The composition was prepared using a compound represented by the chemical formula shown below, and the physical properties thereof were measured. The results are shown in Table 1.

The numerical values of the respective formulas of Table 1 indicate the ratio (unit: mass%) of each compound contained in each composition.

In Comparative Example 1, the compound represented by the formula (i) (the compound represented by the formula (37.2)) contained in the liquid crystal composition of Example 1 was replaced with the liquid crystal composition of the compound represented by the formula (28.3). When the physical property values of Example 1 and Comparative Example 1 were compared, Tni was lowered when the compound represented by the general formula (i) was not contained. Therefore, Example 1 has a high temperature of Tni and can be used in a wide temperature range.

In Comparative Example 2, the compound represented by the formula (II) (the compound represented by the formula (44.1) and the formula (44.2)) contained in the liquid crystal composition of Example 1 was replaced with the compound represented by the formula (45.2). Liquid crystal composition. When the results of Example 1 and Comparative Example 2 were compared, when the compound represented by the formula (ii) was not contained, the Tni system was greatly lowered, and although Δn and Δε were large, the value of γ1 was increased. .

[Examples 2 to 4]

The composition was prepared using a compound represented by the chemical formula shown below, and the physical properties thereof were measured. The results are shown in Table 2.

The numerical values of the respective formulas of Table 2 indicate the ratio (unit: mass%) of each compound contained in each composition.

[Example 5, Comparative Examples 3 to 4]

The composition was prepared using a compound represented by the chemical formula shown below, and the physical properties thereof were measured. The results are shown in Table 3.

The numerical values of the respective formulas of Table 3 indicate the ratio (unit: mass%) of each compound contained in each composition.

In Comparative Example 3, the compound represented by the formula (i) (the compound represented by the formula (39.2) and the formula (38.2)) contained in the liquid crystal composition of Example 5 was replaced with the formula (45.2) and the formula (31.2). A liquid crystal composition of the compound shown. When the physical property values of Example 5 and Comparative Example 3 were compared, when the compound represented by the general formula (i) was not contained, the value of η and the value of γ1 significantly increased. Therefore, Example 5 has a low viscosity and is used in a liquid crystal display element to obtain a fast reaction rate.

In Comparative Example 4, the compound represented by the formula (II) (the compound represented by the formula (44.1) and the formula (44.2)) contained in the liquid crystal composition of Example 5 was replaced with the formula (28.3) and the formula (45.2). Liquid crystal composition of the compound shown) Things. When the results of Example 5 and Comparative Example 4 were compared, when the compound represented by the formula (ii) was not contained, Tni decreased, and Δn and Δε also decreased.

[Examples 6 to 8]

The composition was prepared using a compound represented by the chemical formula shown below, and the physical properties thereof were measured. The results are shown in Table 4.

The numerical values of the respective formulas of Table 4 indicate the ratio (unit: mass%) of each compound contained in each composition.

[Example 9 and Comparative Examples 5 to 6]

The composition was prepared using a compound represented by the chemical formula shown below, and the physical properties thereof were measured. The results are shown in Table 5.

The numerical values of the respective formulas of Table 5 indicate the ratio (unit: mass%) of each compound contained in each composition.

In Comparative Example 5, the compound represented by the formula (i) (the compound represented by the formula (37.2) and the formula (39.2)) contained in the liquid crystal composition of Example 9 was replaced with the formula (44.2) and the formula (28.5). And a liquid crystal composition of the compound represented by the formula (44.1). When the physical property values of Example 9 and Comparative Example 5 were compared, when the compound represented by the formula (i) was not contained, the temperature of Tni was remarkably lowered. Therefore, Example 9 has a high temperature of Tni and can be used in a wide temperature range.

In Comparative Example 6, the compound represented by the formula (II) (the compound represented by the formula (44.1) and the formula (44.2)) contained in the liquid crystal composition of Example 9 was replaced with the formula (45.2) and the formula (28.3). ), as shown in equations (28.5) and (39.2) A liquid crystal composition of the compound. When the results of Example 9 and Comparative Example 6 were compared, when the compound represented by the formula (ii) was not contained, Tni was lowered, and Δε was also decreased.

[Examples 10 to 12]

The composition was prepared using a compound represented by the chemical formula shown below, and the physical properties thereof were measured. The results are shown in Table 6.

The numerical values of the respective formulas of Table 6 indicate the ratio (unit: mass%) of each compound contained in each composition.

[Examples 13 to 15]

The composition was prepared using a compound represented by the chemical formula shown below, and the physical properties thereof were measured. The results are shown in Table 7.

The numerical values of the respective formulas of Table 7 indicate the ratio (unit: mass%) of each compound contained in each composition.

[Examples 16 to 18]

The composition was prepared using a compound represented by the chemical formula shown below, and the physical properties thereof were measured. The results are shown in Table 8.

The numerical values of the respective formulas of Table 8 indicate the ratio (unit: mass%) of each compound contained in each composition.

[Examples 19 to 21]

The composition was prepared using a compound represented by the chemical formula shown below, and the physical properties thereof were measured. The results are shown in Table 9.

The numerical values of the respective formulas of Table 9 indicate the ratio (unit: mass%) of each compound contained in each composition.

The initial VHR of the liquid crystal composition described in each Example, the VHR after heating (150 ° C, 1 hour), the evaluation of the imprint, the evaluation of the volatility, the evaluation of the process suitability, and the evaluation of the solubility at a low temperature were described.

Further, the liquid crystal compositions of the other examples other than Examples 2, 6, 9, 10, 13, 16, and 19 shown in the above table were also evaluated in the same manner, and good results were obtained.

The present invention is not limited to the scope of the present invention, and may be added, omitted, substituted, or otherwise modified without departing from the spirit and scope of the invention. Further, the present invention is not limited by the embodiments, and is only limited by the scope of the claims.

[Industrial availability]

The liquid crystal composition of the present invention can be widely applied to the fields of liquid crystal display elements and liquid crystal displays.

Claims (8)

And a liquid crystal composition containing one or more of the compounds represented by the following formula (i), and one or more of the compounds represented by the following formula (ii), Containing a compound represented by the following formula (L), (wherein R ^11a and R ^21a each independently represent an alkyl group having 1 to 8 carbon atoms, and one of the alkyl groups or two or more non-adjacent-CH ₂ - groups may independently be -CH =CH-, -C≡C-, -O-, -CO-, -COO- or -OCO-, wherein one or more hydrogen atoms in the alkyl group are each independently a fluorine atom or Substituted with a chlorine atom, m ¹¹ represents 1 or 2, and A ¹¹ represents a trans-1,4-cyclohexylene group or a 1,4-phenylene group in which a hydrogen atom may be substituted by a fluorine atom or a chlorine atom, but when m ¹¹ is 1 When A ¹¹ represents a 1,4-phenylene group in which a hydrogen atom may be substituted by a fluorine atom or a chlorine atom, when m ¹¹ is 2, the plural A ¹¹ groups may be the same or different, but at least one of them may represent a hydrogen atom. a 1,4-phenyl group substituted by a fluorine atom or a chlorine atom, X ¹¹ represents a hydrogen atom, a fluorine atom or a chlorine atom, and X ¹² represents a hydrogen atom, a fluorine atom, a chlorine atom, a cyano group, -CF ₃ or -OCF ₃ m ²¹ represents 0 or 1, X ²¹ , X ²² , X ²³ and X ²⁴ each independently represent a hydrogen atom, a fluorine atom or a chlorine atom, and X ²⁵ represents a hydrogen atom, a fluorine atom, a chlorine atom, a cyano group, -CF ₃ Or -OCF ₃ , R ^L1 and R ^L2 each independently represent an alkyl group having 1 to 8 carbon atoms, One or non-contiguous two or more -CH ₂ - groups in the alkyl group may each independently be -CH=CH-, -C≡C-, -O-, -CO-, -COO- or -OCO - Substitution, OL represents 0, 1, 2 or 3, and B ^L1 , B ^L2 and B ^L3 each independently represent a radical selected from (a) 1,4-cyclohexylene (one -CH ₂ - present in this group or Two or more non-contiguous -CH ₂ - may be substituted into -O-) and (b) 1,4-phenylene (one -CH= or two or more adjacent in this group) CH= may be substituted into a group consisting of -N=), and one or two or more hydrogen atoms in the above-mentioned group (a) and (b) may be independently substituted by a cyano group or a fluorine group. Substituted by an atom or a chlorine atom, L ^L1 and L ^L2 each independently represent a single bond, -CH ₂ CH ₂ -, -(CH ₂ ) ₄ -, -OCH ₂ -, -CH ₂ O-, -COO-, -OCO -, -OCF ₂ -, -CF ₂ O-, -CH=NN=CH-, -CH=CH-, -CF=CF- or -C≡C-, when OL is 2 or 3 and L ^L2 is plural When present, they may be the same or different, and when OL is 2 or 3 and B ^L3 is plural, they may be the same or different). The liquid crystal composition of claim 1, wherein m ¹¹ of the formula (i) is 2. A liquid crystal composition according to claim 1 which contains two or more compounds represented by the formula (i). A liquid crystal composition according to claim 1 which contains two or more compounds represented by the formula (ii). A liquid crystal composition according to claim 1 which contains a compound represented by the following formula (M), (wherein R ^M1 represents an alkyl group having 1 to 8 carbon atoms, and one of the alkyl groups or two or more non-adjacent -CH ₂ - groups may independently be -CH=CH-, -C ≡C-, -O-, -CO-, -COO- or -OCO-substituted, PM represents 0, 1, 2, 3 or 4, and C ^M1 and C ^M2 are each independently selected from (d) 1, 4 - a cyclohexyl group (one -CH ₂ - or two or more -CH ₂ - which are not adjacent in this group may be substituted into -O- or -S-) and (e) 1,4-phenylene a group in the group consisting of one (CH============================================================================ One or more hydrogen atoms in the group may be independently substituted by a cyano group, a fluorine atom or a chlorine atom, and K ^M1 and K ^M2 each independently represent a single bond, -CH ₂ CH ₂ -, -(CH _{2 ) 4} -, -OCH ₂ -, -CH ₂ O-, -OCF ₂ -, -CF ₂ O-, -COO-, -OCO- or -C≡C-, when PM is 2, 3 or 4 and K ^{When M1} is in the plural, they may be the same or different. When PM is 2, 3 or 4 and the C ^M2 is plural, they may be the same or different, and X ^M1 and X ^M3 each independently represent a hydrogen atom. a chlorine atom or a fluorine atom, X ^M2 represents a hydrogen atom, a fluorine atom, a chlorine atom , cyano, trifluoromethyl, fluoromethoxy, difluoromethoxy, trifluoromethoxy or 2,2,2-trifluoroethyl; however, formula (i) and formula (ii) Except for the compounds shown). A liquid crystal display element using the liquid crystal composition as in the first aspect of the patent application. A liquid crystal display element characterized by being used in any one of an IPS mode, an OCB mode, an ECB mode, a VA mode, or an FFS mode, and using a liquid crystal composition as in the first aspect of the patent application. A liquid crystal display characterized by using a liquid crystal display element as claimed in claim 6 or 7.