TW200540450A - Optical film and preparation method thereof - Google Patents
Optical film and preparation method thereof Download PDFInfo
- Publication number
- TW200540450A TW200540450A TW93115597A TW93115597A TW200540450A TW 200540450 A TW200540450 A TW 200540450A TW 93115597 A TW93115597 A TW 93115597A TW 93115597 A TW93115597 A TW 93115597A TW 200540450 A TW200540450 A TW 200540450A
- Authority
- TW
- Taiwan
- Prior art keywords
- liquid crystal
- group
- item
- patent application
- monomer
- Prior art date
Links
- 239000012788 optical film Substances 0.000 title claims abstract description 32
- 238000002360 preparation method Methods 0.000 title description 3
- 239000004973 liquid crystal related substance Substances 0.000 claims abstract description 54
- 239000000178 monomer Substances 0.000 claims abstract description 48
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims abstract description 30
- 239000010408 film Substances 0.000 claims abstract description 19
- 235000012000 cholesterol Nutrition 0.000 claims abstract description 15
- 239000000758 substrate Substances 0.000 claims abstract description 14
- 150000001875 compounds Chemical class 0.000 claims abstract description 12
- 229920000642 polymer Polymers 0.000 claims abstract description 7
- 239000000203 mixture Substances 0.000 claims description 42
- 238000009472 formulation Methods 0.000 claims description 38
- 239000004988 Nematic liquid crystal Substances 0.000 claims description 32
- 239000004986 Cholesteric liquid crystals (ChLC) Substances 0.000 claims description 30
- 230000001588 bifunctional effect Effects 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 14
- -1 palmitic compound Chemical class 0.000 claims description 8
- 125000005843 halogen group Chemical group 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 239000002952 polymeric resin Substances 0.000 claims description 5
- 229920005989 resin Polymers 0.000 claims description 5
- 239000011347 resin Substances 0.000 claims description 5
- 229920003002 synthetic resin Polymers 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 238000006243 chemical reaction Methods 0.000 claims description 3
- 239000011248 coating agent Substances 0.000 claims description 3
- 238000000576 coating method Methods 0.000 claims description 3
- 230000001678 irradiating effect Effects 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 claims description 3
- 239000005020 polyethylene terephthalate Substances 0.000 claims description 3
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 125000005529 alkyleneoxy group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 238000010438 heat treatment Methods 0.000 claims description 2
- 229920005668 polycarbonate resin Polymers 0.000 claims description 2
- 239000004431 polycarbonate resin Substances 0.000 claims description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical group CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims 2
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 125000005133 alkynyloxy group Chemical group 0.000 claims 1
- VUWZPRWSIVNGKG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH2] VUWZPRWSIVNGKG-UHFFFAOYSA-N 0.000 claims 1
- 239000003999 initiator Substances 0.000 claims 1
- 235000014655 lactic acid Nutrition 0.000 claims 1
- 239000004310 lactic acid Substances 0.000 claims 1
- 229920005749 polyurethane resin Polymers 0.000 claims 1
- 239000007788 liquid Substances 0.000 abstract description 5
- 230000000379 polymerizing effect Effects 0.000 abstract 1
- 239000000463 material Substances 0.000 description 8
- VFHVQBAGLAREND-UHFFFAOYSA-N diphenylphosphoryl-(2,4,6-trimethylphenyl)methanone Chemical compound CC1=CC(C)=CC(C)=C1C(=O)P(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 VFHVQBAGLAREND-UHFFFAOYSA-N 0.000 description 5
- 238000001228 spectrum Methods 0.000 description 5
- 229920000106 Liquid crystal polymer Polymers 0.000 description 4
- 238000005282 brightening Methods 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- 230000010287 polarization Effects 0.000 description 4
- 239000005441 aurora Substances 0.000 description 3
- 230000003098 cholesteric effect Effects 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000010586 diagram Methods 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- OKWOTJDKZXEOHN-UHFFFAOYSA-N CC(C=C1C)=CC(C)=C1P.O=P(C1=CC=CC=C1)C1=CC=CC=C1 Chemical compound CC(C=C1C)=CC(C)=C1P.O=P(C1=CC=CC=C1)C1=CC=CC=C1 OKWOTJDKZXEOHN-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 239000004977 Liquid-crystal polymers (LCPs) Substances 0.000 description 1
- NIPNSKYNPDTRPC-UHFFFAOYSA-N N-[2-oxo-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 NIPNSKYNPDTRPC-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 125000005055 alkyl alkoxy group Chemical group 0.000 description 1
- 210000000941 bile Anatomy 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 238000001354 calcination Methods 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 229920006254 polymer film Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 238000001429 visible spectrum Methods 0.000 description 1
Landscapes
- Liquid Crystal (AREA)
- Liquid Crystal Substances (AREA)
Abstract
Description
200540450 玖、發明說明: 【發明所屬之技術領域】 本發明係關於一種光學膜,其包含一透明基材及至少一 層膽固醇型液晶聚合物塗佈於基材之表面,以作為液晶顯 示器之偏光片。由於本發明光學膜可利用多層堆疊以調整 其反射波頻寬,因此可有效提升液晶顯示器之亮度,且適 用於頻寬廣或特殊頻寬範圍之液晶顯示器。 【先前技術】 偏光片係指一選擇性讓特定方向的光通過的光學材料, 主要用於將一般非極化光轉變為偏極光。其作用方式是當 照射非極化之一般光源時,只允許兩正交線性光軸其中之 一方向通過,但另一轴向之光則將被偏光片所吸收,用以 控制特定光波的偏振方向。 在一般液晶顯示器結構中,液晶面板前後必須貼合兩片 正父之偏光片’由於液晶本身不具使光通過、遮蔽的控制 功能’需藉助偏光片來達成相關功能,才能有效控制每一 晝素的亮與暗狀態。標準偏光片使用吸附的方式加以過滤 光源’這種偏光片的缺點在於最佳狀態下僅有最高$ 的 入射光此轉化為線性偏極光,因此造成光源損失,使液晶 顯示器亮度不足,亦間接影響燈管之使用期限。此類型偏 光片的另一個缺點在於未穿透之光源部份,此部份被吸收 光源對於偏光片將轉變成大量的熱能,進而造成偏光片性 貝的不可預測之改變,尤其在高能量入射光下甚至可能引 發偏光片結構的破壞。200540450 发明 Description of the invention: [Technical field to which the invention belongs] The present invention relates to an optical film comprising a transparent substrate and at least one layer of a cholesteric liquid crystal polymer coated on the surface of the substrate as a polarizer for a liquid crystal display. . Since the optical film of the present invention can utilize multiple layers to adjust its reflected wave bandwidth, it can effectively increase the brightness of the liquid crystal display, and is suitable for liquid crystal displays with a wide bandwidth or a special bandwidth range. [Prior Art] A polarizer refers to an optical material that selectively allows light in a specific direction to pass through. It is mainly used to convert general unpolarized light into polarized light. Its mode of action is that when irradiating a non-polarized general light source, only one of the two orthogonal linear optical axes is allowed to pass, but the light in the other axis will be absorbed by a polarizer to control the polarization direction of a specific light wave. . In a general LCD display structure, two positive and negative polarizers must be attached to the front and back of the LCD panel. "Since the liquid crystal itself does not have the control function to allow light to pass through and block it," polarizers are required to achieve related functions in order to effectively control each element. Light and dark states. Standard polarizers use an adsorption method to filter the light source. The disadvantage of this polarizer is that in the best state, only the highest $ of incident light is converted into linear polarized light, which results in loss of light source and insufficient brightness of the liquid crystal display. Life of the lamp. Another disadvantage of this type of polarizer is the part of the light source that is not penetrated. This part of the absorbed light source will transform the polarizer into a large amount of thermal energy, which will cause unpredictable changes in polarizer properties, especially at high energy incidence. Under light, the structure of the polarizer may even be damaged.
O:\90\90609.DOC 200540450 為解決上述問題,業界發展出一種膽固醇型光學臈來回 收原本必須損失掉的光能量。所謂膽固醇型液晶係為一種 結構相似於膽固醇分子的液晶。膽固醇型液晶主要是由向 列型(nematics)液晶堆積所形成,在向列型液晶中加入掌性 化合物(chiral compound),會使向列型液晶分子的長軸方向 漸次相差一個角度旋轉而成螺旋狀,這種結構跟膽固醇分 子相似,因此稱此類液晶為膽固醇型液晶。 圖1為習知傳統顯示(I)及具有膽固醇型光學膜之顯示(π) 之液晶顯示器之示意圖。如圖丨所示,由下至上依序為反射 板10、導光板12、具左旋化學結構之膽固醇液晶光學膜 (CLC)14、λ/4相位差板16、下層偏光片18、液晶層2〇及上 層偏光片22。當光源24點亮時,光線經導光板12擴散,當 光線經過膽固醇液晶光學膜14時,此時僅允許右旋光通 過’並將左方疋光反射回光源方向,而通過之右旋光則由圓 偏極光轉變為橢圓偏極光,因此需要再通過相位差板16, 將光線修正為線性偏極光,此類型光線便可應用於液晶顯 示器系統。另一方面,反射至光源方向之左旋光則經由反 射板10反射後,轉化為右旋光,當其再一次行經膽固醇液 晶光學膜14時,因旋光性已改變而可順利通過。因此,當 膽固醇液晶光學膜存在時,光源進入液晶面板前已悉數轉 化為單一方向之線性偏極光,而不會造成光源的大量損 失。因此稱此種膽固醇液晶光學膜為膽固醇型偏光片,期 望能取代傳統之偏光片。但事實上並不容易做到,因為膽 口醇型偏光片所通過之光線經相位差板後,並無法得到與O: \ 90 \ 90609.DOC 200540450 In order to solve the above problems, the industry has developed a cholesterol-based optical chirp to recover the light energy that must be lost. The so-called cholesteric liquid crystal system is a liquid crystal whose structure is similar to that of cholesterol molecules. Cholesterol liquid crystal is mainly formed by the accumulation of nematic liquid crystals. Adding a chiral compound to nematic liquid crystals will gradually rotate the nematic liquid crystal molecules by an angle of one angle. Spiral, this structure is similar to cholesterol molecules, so this type of liquid crystal is called cholesterol-type liquid crystal. FIG. 1 is a schematic diagram of a conventional conventional display (I) and a liquid crystal display (π) with a cholesteric optical film. As shown in Figure 丨, from bottom to top are the reflection plate 10, the light guide plate 12, the cholesteric liquid crystal optical film (CLC) 14 with a left-handed chemical structure, the λ / 4 retardation plate 16, the lower polarizer 18, and the liquid crystal layer 2. 〇 and upper polarizer 22. When the light source 24 is lit, the light diffuses through the light guide plate 12, and when the light passes through the cholesteric liquid crystal optical film 14, only right-handed light is allowed to pass through and the left chirped light is reflected back to the direction of the light source, while the right-handed light passes through The circular polarized aurora is transformed into an elliptical polarized aurora. Therefore, it is necessary to correct the light to a linear polarized aurora through the phase difference plate 16. This type of light can be applied to a liquid crystal display system. On the other hand, the left-handed light reflected to the direction of the light source is reflected by the reflecting plate 10 and converted into right-handed light. When it passes through the cholesterol liquid crystal optical film 14 again, the optical rotation can be passed smoothly. Therefore, when a cholesteric liquid crystal optical film exists, the light source has been fully converted into a linear polarized polarized light in a single direction before entering the liquid crystal panel, without causing a large loss of the light source. Therefore, this kind of cholesteric liquid crystal optical film is called a cholesteric polarizer, and it is expected to replace the traditional polarizer. But in fact, it is not easy to do, because the light passing through the bile polarizer can not get
O:\90\90609.DOC 200540450 傳統偏光片相同程度的線性偏光,亦即其偏光度不足,此 光線直接進入液晶面板後將造成嚴重的漏光現象。因此, 目前業界做法為將膽固醇液晶光學膜、相位差板及偏光片 二者同時貼合,不但可以保證光源之偏光度,也可大幅提 高光源之有效利用度。這種膽固醇液晶光學膜目前便被稱 之為增亮膜。 此外’根據麥克斯威爾(Maxwell)理論:λ==ηχρ,其中入 為液aa 了反射之波長,η為材料的折射率,且ρ為螺距。 由於液晶具有雙折射之性質,上式可修正為·· zU=(ne — η0)χρ=Δηχρ,其中^為反射波之頻寬,〜為液晶材料折射 率,且η。為一般折射率。 然而就實用性而言,可見光頻寬約為250 nm,但一般液 晶的Δη值約為0」〜0.2,故其頻寬約為5〇〜1〇〇 nm,遠小於 可見光頻寬,因此須使用不同液晶材料所製之增亮膜,做 多層堆疊方可應用,造成此製程煩瑣複雜。所以,如何解 決增亮膜作用頻寬過小,成了顯示器業界重要課題。O: \ 90 \ 90609.DOC 200540450 The same degree of linear polarization of traditional polarizers, that is, its polarization is insufficient. This light will cause serious light leakage after entering the LCD panel. Therefore, the current industry practice is to attach the cholesteric liquid crystal optical film, retardation plate and polarizer at the same time, which can not only ensure the polarization of the light source, but also greatly improve the effective utilization of the light source. This cholesteric liquid crystal optical film is currently called a brightness enhancement film. In addition, according to Maxwell's theory: λ == ηχρ, where is the reflection wavelength of liquid aa, η is the refractive index of the material, and ρ is the pitch. Because of the birefringent nature of liquid crystals, the above formula can be modified as: zU = (ne — η0) χρ = Δηχρ, where ^ is the frequency bandwidth of the reflected wave, ~ is the refractive index of the liquid crystal material, and η. Is the general refractive index. However, in terms of practicality, the visible light bandwidth is about 250 nm, but the Δη value of a general liquid crystal is about 0 "~ 0.2, so its bandwidth is about 50 ~ 100nm, which is much smaller than the visible light bandwidth. The brightness enhancement films made of different liquid crystal materials can be used for multi-layer stacking, making this process cumbersome and complicated. Therefore, how to solve the problem that the bandwidth of the brightness enhancement film is too small has become an important issue in the display industry.
Dreher 在 Solid State Communication (Vol· 12, 519-522, 1973)、Mazkedian等人在 j. Physique c〇11〇q (ν〇: 36,ΡΡ· Ci-283, 1974)及 Hajd0等人在 j 〇pt s〇c Am (ν〇ι_ 36,PP_ 1017, 1976)中所做的研究指出,在縱深方向具梯度 分佈變化之螺距的螺旋狀結構可有效的得到寬廣反射波^ 寬。 歐洲專利案EP 0 606 940 A2曾提出以不同單體(掌性與 非掌性化合物)聚合,因擴散效應而產生連續梯度分佈之螺Dreher in Solid State Communication (Vol. 12, 519-522, 1973), Mazkedian et al. In j. Physique c〇11〇q (ν〇: 36, PP · Ci-283, 1974) and Hajd0 et al. In j 〇 A study made in pt soc Am (ν〇ι_36, PP_1017, 1976) pointed out that a spiral structure with a spiral pitch with a gradient distribution change in the depth direction can effectively obtain a wide reflected wave ^. European patent EP 0 606 940 A2 has proposed the use of different monomers (palm and non-palm compounds) to polymerize, resulting in a continuous gradient distribution of spirals due to diffusion effects.
O:\90\90609.DOC 200540450 2值。但若要得到具有較廣頻寬之產品,則必_外添加 染枓來造成光源強度隨薄膜縱向深度不同而有所差異。此 方法的缺點為以低能量光源做長時間曝光來控制螺距分 佈’對於膜厚的要求極為嚴苛。 另外 Pmdak等人於PhyS. Rev· Lett (v〇1 32,pp 43, 1974) 中θ揭不以控制溫度梯度的方式來控制膽固醇衍生物質的 螺距變化’但由於高分子薄膜之導熱性質良好,製作過程 中的溫度梯度極難做有效的控制,成為此方法重要的缺點。 、本案發明人經廣泛研究發現,膽固醇型液晶聚合物所製 成之光學膜,#用其配方之單體摻混比例不同’可得不同 之反射波。㈣多層_疊使其反射波頻寬可涵蓋可見光頻 寬’能有效解決上述的缺點。 【發明内容】 本發明之目的係提供一種光學膜,其包含高分子樹脂之 透明基材及至少一層膽固醇型液晶聚合物塗佈於該基材之 表面。該光學膜可用於液晶顯示器中作為偏光片,特別是 增壳膜,以提高液晶顯示器之亮度。 本發明之另一目的在於提供一種膽固醇型液晶配方,可 用以形成光學膜。 本發明之又一目的在於提供一種製造光學膜之方法。 【實施方式】 本發明光學膜所使用之高分子樹脂並無特殊限制,其可 :、、、κ -日树月曰(p〇iyester resin)、聚碳酸酉旨樹脂(p〇iycarb〇nate resin)或♦月女基甲酸酯樹脂(p〇1yurethane resin)或其混合O: \ 90 \ 90609.DOC 200540450 2 value. However, if you want to obtain a product with a wide bandwidth, you must add external dye to cause the intensity of the light source to vary with the vertical depth of the film. The disadvantage of this method is that the long-term exposure with a low-energy light source to control the pitch distribution 'has extremely strict requirements for film thickness. In addition, Pmdak et al. In PhyS. Rev. Lett (v〇1 32, pp 43, 1974) θ does not control the change in the pitch of cholesterol-derived substances by controlling the temperature gradient. However, due to the good thermal conductivity of polymer films, It is extremely difficult to effectively control the temperature gradient in the production process, which has become an important disadvantage of this method. 2. The inventors of this case have found through extensive research that different reflected waves can be obtained for optical films made from cholesterol-type liquid crystal polymers. The multi-layer stack can make the reflected wave bandwidth cover the visible light bandwidth ', which can effectively solve the above disadvantages. SUMMARY OF THE INVENTION The object of the present invention is to provide an optical film, which comprises a transparent substrate including a polymer resin and at least one layer of a cholesteric liquid crystal polymer coated on the surface of the substrate. The optical film can be used as a polarizer in a liquid crystal display, especially a shell-enlarging film to improve the brightness of the liquid crystal display. Another object of the present invention is to provide a cholesteric liquid crystal formulation which can be used to form an optical film. Another object of the present invention is to provide a method for manufacturing an optical film. [Embodiment] There is no particular limitation on the polymer resin used in the optical film of the present invention, and it can be: ,,, κ-sun tree month (p0yyester resin), polycarbonate resin (p0yycarb〇nate resin) ) Or ♦ yurethane resin (p〇1yurethane resin) or its mixture
O:\90\90609.DOC 200540450 物,較佳為聚對苯二甲酸乙二酯(PET)。 本發明之膽固醇型液晶聚合物,係由一膽固醇型液晶配 方所聚合而成,該配方包含: (1) 單官能基向列型液晶單體; (2) 雙官能基向列型液晶單體; (3) 掌性化合物單體;及 (4) 光起始劑。 本發明中可用於形成聚合物之單官能基向列型液晶單體 及雙官能基向列型液晶單體可分別選自由具以下結構式所 組成之群組·O: \ 90 \ 90609.DOC 200540450, preferably polyethylene terephthalate (PET). The cholesteric liquid crystal polymer of the present invention is polymerized from a cholesteric liquid crystal formulation, which comprises: (1) a monofunctional nematic liquid crystal monomer; (2) a bifunctional nematic liquid crystal monomer (3) Palm compound monomer; and (4) Photoinitiator. The monofunctional nematic liquid crystal monomer and the bifunctional nematic liquid crystal monomer that can be used to form a polymer in the present invention can be selected from the group consisting of the following structural formulas, respectively:
(1)單官能基向列型液晶單體 CH2=CH—C—0—R—Ar—X δ 〒η3(1) Monofunctional nematic liquid crystal monomer CH2 = CH—C—0—R—Ar—X δ 〒η3
CH2=C—C—Ο—R—Ar——X O /〇\CH2 = C—C—〇—R—Ar——X O / 〇 \
CH2—CH—R—Ar——X (2)雙官能基向列型液晶單體 CH2=CH—C—0—R—Ar—R—〇一C—ChNCH2 π 11 〇 〇 CH3 ch3 CH2=C C —〇—R—Ar—R—〇一C—C=CH2 11 11 〇 〇 O:\90\90609.DOC -10- 200540450CH2—CH—R—Ar——X (2) Bifunctional nematic liquid crystal monomer CH2 = CH—C—0—R—Ar—R—〇—C—ChNCH2 π 11 〇〇CH3 ch3 CH2 = CC —〇—R—Ar—R—〇—C—C = CH2 11 11 〇〇O: \ 90 \ 90609.DOC -10- 200540450
CH2—CH 八 一 R—Ar—R—CH—CH2 其中,尺為Ci-Cn伸烷基或Ci-Cw伸烷氧基,X為選自由氛 基、Ci-Cio烧氧基及心/㈠烧基所組成之群組之一末端基, 且Ar為選自由以下具液晶相之團基所組成之群組: <〇^~n=n~<〇>-、—CH=CH——CH2—CH Bayi R—Ar—R—CH—CH2 where Ci is a Ci-Cn alkyl or Ci-Cw alkyl alkoxy group, and X is selected from the group consisting of aryl, Ci-Cio, and oxo A terminal group of a group consisting of a calcining group, and Ar is selected from the group consisting of the following groups having a liquid crystal phase: < 〇 ^ ~ n = n ~ < 〇 >-, -CH = CH ——
Or 试 ^Qr、Or try ^ Qr,
及and
AA
AA
其中,A為選自由自氫原子、Ci-C6烧基及鹵素原子所組 O:\9O\906O9.DOC -11 - 200540450 成之群組之另一末端基。 本發明中可用於形成聚合物之掌性化合物單體,係單官 能基掌性化合物單體,可選自由具以下結構式所組成之群 組: CH2=Ch^C—0—R—Ar—丫Among them, A is another terminal group selected from the group consisting of a hydrogen atom, a Ci-C6 alkyl group, and a halogen atom O: \ 9O \ 906O9.DOC -11-200540450. The palm compound monomer that can be used to form a polymer in the present invention is a monofunctional palm compound monomer, and can be selected from the group consisting of the following structural formula: CH2 = Ch ^ C—0—R—Ar— Ya
II 〇 ch3II 〇 ch3
CH2=C—c—Ο —R—Ar-YCH2 = C—c—Ο —R—Ar-Y
II 〇 〇 /\II 〇 〇 / \
CH2一CH2一R一Ar一Y 其中,11為0:1-(^()伸烷基伸烷氧基,X為選自由氰 基、Ci-Cio烷氧基及心/⑺烷基所組成之群組之一末端基, 且Ar為選自以下具液晶相之團基所組成之群組:CH2—CH2—R—Ar—Y, where 11 is 0: 1-(^ () alkylene and alkyleneoxy, and X is selected from the group consisting of cyano, Ci-Cioalkoxy, and cardio / fluorenyl One terminal group of the group, and Ar is selected from the group consisting of the following groups having a liquid crystal phase:
O:\90\9O6O9.DOC -12- 200540450O: \ 90 \ 9O6O9.DOC -12- 200540450
其中’ A為選自由氫原子、Ci-C6烷基及鹵素原子所組成 之群組之另一末端基;其中Y為選自由膽固醇、 〇Where 'A is another terminal group selected from the group consisting of a hydrogen atom, a Ci-C6 alkyl group, and a halogen atom; wherein Y is selected from the group consisting of cholesterol, 〇
II U 一 C—O 〇II U-C—O 〇
之可以形成液晶相之旋光性團基。 、溴或碘原子。 单官能基向列型液 在本發明中,鹵素原子可以為氟、氣 此外,在本發明之較佳實施態樣中, 晶單體,可為具以下結構式者:It can form optically active group of liquid crystal phase. , Bromine or iodine atom. Monofunctional nematic liquid In the present invention, the halogen atom may be fluorine or gas. In addition, in a preferred embodiment of the present invention, the crystalline monomer may be one having the following structural formula:
式(A)Formula (A)
O:\90\90609.DOC -13- 200540450 在本發明之較佳實施態樣中,雙官能基向列型液晶單 體,可為選自下列結構式者: ch2=ch -ο—(ch2)「o-O: \ 90 \ 90609.DOC -13- 200540450 In a preferred embodiment of the present invention, the bifunctional nematic liquid crystal monomer may be selected from the following structural formulas: ch2 = ch -ο— (ch2 ) "O-
C2H5 ch=ch2 ^ -〇—(ch2)6—o—《 式(B) CH2=CHn C1 -c-o—^ o-c ch=ch2 、 -o—(CH2)6-o-d 式(C) 在本發明之較佳實施態樣中,單官能基掌性化合物單 體,可為選自下列結構式者: 。-C2H5 ch = ch2 ^ -〇— (ch2) 6—o— 《Formula (B) CH2 = CHn C1 -co— ^ oc ch = ch2, -o— (CH2) 6-od Formula (C) In the present invention In a preferred embodiment, the monofunctional palm compound monomer may be selected from the following structural formulas: -
h2c=c- 在本發明之膽固醇型液晶配方中,單官能基向列型液晶 單體係佔膽固醇型液晶配方之約30至60重量百分比(wt%),較 佳為約40至50 wt% ;雙官能基向列型液晶單體係佔膽固醇 型液晶配方之約30至60 wt%,較佳為約40至50 wt% ;而掌性 化合物單體係佔膽固醇型液晶配方之約1至20 wt%,較佳為 約 5至 15 wt%。 本發明可用於形成聚合物之光起始劑,係熟習此項技術 之人士所熟知者,例如但不限於2,4,6-三甲基苯曱醯二苯基 膦氧化物(2,4,6_trimethyl benzoyl diphenyl phosphine oxide,TPO)。在本發明之膽固醇型液晶配方中,光起始劑 係佔膽固醇型液晶配方之約0.1至10 wt%,較佳為約1至5 wt%。 O:\90\90609.DOC -14- 200540450 本發明之贍固醇型液晶配方可視需要添加各種添加劑, 如平坦劑,例如但不限於丙烯酸酯共聚物,Βγκ_36ΐ。在 本發明之膽固醇型液晶配方中,添加劑之用量係佔膽固醇 型液晶配方之約〇,〇5至5 wt%,較佳為約〇·ι至2 wt〇/〇。 由本發明膽固醇型液晶配方所製得之聚合物,可用於液 晶顯示器中作為光學膜之材料,此光學膜可作為增亮膜之 用途。 此外,本發明另提供一種製備光學膜之方法,其包含以 下步驟: (a) 將向列型液晶單體和掌性化合物單體摻混,然後加 入光起始劑,以形成一膽固醇型液晶配方; (b) 將膽固醇型液晶配方塗佈於一透明基材上; (c) 於常溫或加熱下,對膽固醇型液晶配方照射能量射 線以進行光聚合反應。 在本發明製備方法中,將膽固醇型液晶配方進行光聚合 所使用的能量射線,泛指一定範圍波長之光源,例如紫外 光、紅外光、可見光或熱線(放射或輻射)等,較佳為紫外光, 照光強度為約〇.1至10瓦特/平方公分(w/cm2),較佳為1至5 W/cm2。 在本鲞明製備方法中,塗佈步驟或聚合反應步驟的溫度 控制在約20至40°C,較佳為約3〇〇c。 塗佈於透明基材上之膽固醇型液晶配方之厚度為約2至 25你i:米,較佳為約3至1〇微米。可視需要重複進行上述方法 以於透明基材上重複增| ’使所製#寻的光學膜具有較大範h2c = c- In the cholesterol type liquid crystal formulation of the present invention, the monofunctional nematic liquid crystal single system accounts for about 30 to 60 weight percent (wt%) of the cholesterol type liquid crystal formulation, preferably about 40 to 50 wt% ; Bifunctional nematic liquid crystal single system accounts for about 30 to 60 wt%, preferably about 40 to 50 wt% of cholesterol-based liquid crystal formulations; and palmitic compound single systems account for about 1 to about cholesterol-based liquid crystal formulations 20 wt%, preferably about 5 to 15 wt%. The photoinitiator useful in the present invention for forming polymers is well known to those skilled in the art, such as, but not limited to, 2,4,6-trimethylphenylphosphonium diphenylphosphine oxide (2,4 , 6_trimethyl benzoyl diphenyl phosphine oxide (TPO). In the cholesteric liquid crystal formulation of the present invention, the photoinitiator accounts for about 0.1 to 10 wt%, preferably about 1 to 5 wt% of the cholesterol liquid crystal formulation. O: \ 90 \ 90609.DOC -14- 200540450 The sterol-type liquid crystal formulation of the present invention may add various additives, such as a flattening agent, such as, but not limited to, an acrylate copolymer, Bγκ_36ΐ, as required. In the cholesteric liquid crystal formulation of the present invention, the amount of the additive is about 0.05 to 5 wt%, preferably about 0.00 to 2 wt%. The polymer prepared by the cholesteric liquid crystal formulation of the present invention can be used as a material for an optical film in a liquid crystal display, and the optical film can be used as a brightness enhancement film. In addition, the present invention further provides a method for preparing an optical film, which includes the following steps: (a) blending a nematic liquid crystal monomer and a palm compound monomer, and then adding a photoinitiator to form a cholesterol-type liquid crystal Formulation; (b) coating the cholesterol-type liquid crystal formula on a transparent substrate; (c) irradiating the cholesterol-type liquid crystal formula with energy rays at normal temperature or under heating for photopolymerization reaction. In the preparation method of the present invention, the energy ray used for photopolymerizing the cholesterol-type liquid crystal formulation generally refers to a light source with a certain range of wavelengths, such as ultraviolet light, infrared light, visible light, or hot rays (radiation or radiation), and preferably ultraviolet light. The light has a light intensity of about 0.1 to 10 watts per square centimeter (w / cm2), preferably 1 to 5 W / cm2. In the preparation method of the present invention, the temperature of the coating step or the polymerization reaction step is controlled at about 20 to 40 ° C, preferably about 300c. The thickness of the cholesteric liquid crystal formulation coated on the transparent substrate is about 2 to 25 μm, preferably about 3 to 10 μm. The above method can be repeated as needed to repeatedly increase the transparent substrate |
O:\90\90609.DOC -15- 200540450 圍的可見光頻寬。 以下實施例將對本發明做進一步 制本發明之實施範圍,任何熟 ’但並非用以限 違背本發明之精神下所得以達:二技術領域者,在不 “Hi 達成之修飾及變化,均屬於本 發明之範圍 實施例 本發明實施例中所使用之各單體結構如 單官能基向列型液晶單體(a) 下:O: \ 90 \ 90609.DOC -15- 200540450 visible light bandwidth. The following examples will further modify the scope of the present invention. Anyone who is familiar with the scope of the present invention is not limited to the spirit of the present invention. Modifications and changes achieved by those who are not "Hi" in the two technical fields belong to Examples of the scope of the present invention Each monomer structure used in the examples of the present invention is, for example, a monofunctional nematic liquid crystal monomer (a):
雙官能基向列型液晶單體(b)Bifunctional nematic liquid crystal monomer (b)
- Ο—(CH2)6—I-Ο— (CH2) 6—I
O—(CH2)6~〇-C^ CH2==CH\ ,ch=ch2 (/ 雙官能基向列型液晶單體(c) ch2==ch )c-ο—(ch2)6—0-O— (CH2) 6 ~ 〇-C ^ CH2 == CH \, ch = ch2 (/ bifunctional nematic liquid crystal monomer (c) ch2 == ch) c-ο— (ch2) 6-0-
ίο-^oJ ch=ch2 單官能基掌性單體(d)ίο- ^ oJ ch = ch2 Monofunctional palm monomer (d)
O 厂-V H2C=C- C~ ^ 〇O plant-V H2C = C- C ~ ^ 〇
Η 實施例1-3 平坦劑及光起始劑 取不同比例的上述單體(a)、(b)與(d)、Η Example 1-3 Plane agent and photoinitiator Take the above monomers (a), (b) and (d),
O:\90\90609.DOC -16- 200540450 以形成膽固醇型液晶配方1、2及3,如表1所示: 表1 液晶配方 1 2 3 單官能基向列型液晶單體(a) 46% 45% 44% 雙官能基向列型液晶單體(b) 46% 98 wt% 45% 98 wt% 44% 98 wt% 單官能基掌性單體(d) ^8% 10% 12% 平坦劑(BYK_361) 1 wt% 1 wt% 1 ^ vt% 光起始劑(TPO) 1 wt% 1 wt% 1 wt% 決定所得到配方反射光色的主要條件在於掌性單體的摻 混比例,所含比例較少者可反射較短波長的紅光區域,反 之則可得藍光,但超出適用含量範圍之組成配方則反射可 見光區域外的紅外光或紫外光,沒有實際價值。 將液晶配方1、2與3分別以本發明之製作方法形成光學 膜’以作為單色增免膜。圖2為本發明之實施例1至3中之膽 固醇型液晶配方1至3之反射波段頻寬之光譜,分別以I、η 及III表示。其中,配方1為紅光波段增亮膜,有效波長範圍 約為576至694毫微米(nm),配方2為綠光波段增亮膜,有效 _ 波長範圍約為492至586 nm,配方3為藍光波段增亮膜,有 效波長範圍約為400至492 nm。 由上述數據顯示,使用本發明之膽固醇型液晶配方所製 得之三層增亮膜的疊加產品,已可有效涵蓋整個可見光頻 寬(有效波長範圍約為426〜686 nm)。 實施例4-9 取不同比例的上述單體(a)、(勹與(d)、平坦劑及光起始劑 以形成膽固醇型液晶配方4至9,如表2所示: O:\90\90609.DOC -17- 200540450 表2 液晶配方 4 5 6 單官能基向列型液晶單體(a) 47.5 % 98 wt% 47% 98wt% 46.5 % 98wt% 雙官能基向列型液晶單體(c) 47.5 % 47% 46.5 % 單官能基掌性單體(d) 5% 6% 7% 平坦劑(BYK-361) 1 wt% 1 wt% 1 wt% 光起始劑(TPO) 1 wt% 1 wt% 1 wt% 液晶配方 7 8 9 單官能基向列型液晶單體(a) 46% 98wt% 45.5 % 98wt% 45% 98wt% 雙官能基向列型液晶單體(c) 46% 45.5 % 45% 單官能基掌性單體(d) 8% 9% 10% 平坦劑(BYK-361) 1 wt% 1 wt% 1 wt% 光起始劑(TPO) 1 wt% 1 wt% 1 wt% 配方4至9係使用與實施例1至3之配方1至3不同之雙官能 基向列型液晶單體,主要差別在於單體(b)為具高雙折射率 值材料,而單體(c)則為具低雙折射率值材料。由前述麥克 斯威爾理論可知材料之雙折射率值可直接影響反射波段之 頻寬,因此,於實施例4至9中所配製配方均具有較窄的反 射波段頻寬,如圖3所示,圖3為本發明之實施例4至9中之 膽固醇型液晶配方4至9之反射波段頻寬之光譜。 因此,若以配方4至9製作全可見光波段增亮膜即必須以 更多光學膜之疊加來表現。舉例言之,可選擇實施例6至9 之增亮膜,利用四層疊加來獲得可見光譜增亮膜。 綜上所述,本發明之膽固醇型液晶配方可利用簡單且容 易控制之製程,靈活由配方組成中製得具有適當的反射波 O:\90\90609.DOC -18 - 200540450 段之增亮膜,不但可有效提升液晶顯示器之亮度,且可利 用多層堆疊以有效涵蓋整個可見光頻寬,以應用於需要全 光譜白光之一般顯示器,或應用於特殊頻寬範圍之特殊顯 示器驅動模式。 以下申請專利範圍係用以界定本發明之合理保護範圍。 然應明瞭者,技藝人士基於本發明之揭示所可達成之種種 顯而易見之改良,亦應歸屬本發明合理之保護範圍。 【圖式簡單說明】 圖1為習知傳統顯示(I)及具有膽固醇型光學膜之顯示(II) 之液晶顯不Is之不意圖。 圖2為本發明之實施例1至3中之膽固醇型液晶配方1至3 之反射波段頻寬之光譜。 圖3為本發明之實施例4至9中之膽固醇型液晶配方1至3 之反射波段頻寬之光譜。 【圖式元件符號之簡單說明】 10 反射板 12 導光板 14 膽固醇液晶光學膜 16 λ/4相位差板 18 下層偏光片 20 液晶層 22 上層偏光片 24 光源 卩八1^¥\新案\90609\90609€5 長興-FINAL.DOC -19-O: \ 90 \ 90609.DOC -16- 200540450 to form cholesterol-type liquid crystal formulations 1, 2 and 3, as shown in Table 1: Table 1 Liquid crystal formulation 1 2 3 Monofunctional nematic liquid crystal monomer (a) 46 % 45% 44% Bifunctional nematic liquid crystal monomer (b) 46% 98 wt% 45% 98 wt% 44% 98 wt% Monofunctional palm monomer (d) ^ 8% 10% 12% Flat Agent (BYK_361) 1 wt% 1 wt% 1 ^ vt% Photoinitiator (TPO) 1 wt% 1 wt% 1 wt% The main condition that determines the reflected light color of the obtained formula is the blending ratio of palm monomers, Those with a small proportion can reflect the red light region with a short wavelength, and vice versa can obtain blue light, but the composition formula that exceeds the applicable content range reflects infrared or ultraviolet light outside the visible light region, which has no practical value. The liquid crystal formulations 1, 2 and 3 were respectively formed into an optical film 'by the manufacturing method of the present invention as a monochromatic anti-remission film. FIG. 2 is a spectrum of the reflection band widths of the cholesteric liquid crystal formulations 1 to 3 in Examples 1 to 3 of the present invention, which are represented by I, η, and III, respectively. Among them, Formula 1 is a red light enhancement film with an effective wavelength range of about 576 to 694 nanometers (nm), and Formula 2 is a green light enhancement film with an effective wavelength range of about 492 to 586 nm. Formula 3 is Blue light band brightening film, effective wavelength range is about 400 to 492 nm. According to the above data, the superimposed product of the three-layer brightness enhancement film prepared by using the cholesterol-type liquid crystal formulation of the present invention can effectively cover the entire visible light bandwidth (effective wavelength range is about 426 to 686 nm). Example 4-9 The above-mentioned monomers (a), (a) and (d), a flattening agent, and a photoinitiator were prepared in different proportions to form cholesterol-type liquid crystal formulations 4 to 9, as shown in Table 2: O: \ 90 \ 90609.DOC -17- 200540450 Table 2 Liquid crystal formulation 4 5 6 Monofunctional nematic liquid crystal monomer (a) 47.5% 98 wt% 47% 98wt% 46.5% 98wt% Bifunctional nematic liquid crystal monomer ( c) 47.5% 47% 46.5% Monofunctional Palm Monomer (d) 5% 6% 7% Planer (BYK-361) 1 wt% 1 wt% 1 wt% Photoinitiator (TPO) 1 wt% 1 wt% 1 wt% liquid crystal formulation 7 8 9 monofunctional nematic liquid crystal monomer (a) 46% 98wt% 45.5% 98wt% 45% 98wt% bifunctional nematic liquid crystal monomer (c) 46% 45.5 % 45% Monofunctional Palm Monomer (d) 8% 9% 10% Planar (BYK-361) 1 wt% 1 wt% 1 wt% Photoinitiator (TPO) 1 wt% 1 wt% 1 wt % Formulas 4 to 9 are bifunctional nematic liquid crystal monomers different from those of Formulas 1 to 3 of Examples 1 to 3. The main difference is that monomer (b) is a material with a high birefringence value, while the monomer (C) is a material with a low birefringence value. According to the aforementioned Maxwell theory, the birefringence value of the material can directly affect the reflection Therefore, the formulas prepared in Examples 4 to 9 all have a narrow reflection band bandwidth, as shown in FIG. 3, which is a cholesterol-type liquid crystal formula in Examples 4 to 9 of the present invention. The spectrum of the reflection band bandwidth of 4 to 9. Therefore, if the full visible light enhancement film is made with the formulas 4 to 9, it must be represented by the superposition of more optical films. For example, the embodiments 6 to 9 can be selected. Brightening film, using four layers of superposition to obtain the visible spectrum brightening film. In summary, the cholesterol-type liquid crystal formulation of the present invention can use a simple and easy-to-control process to flexibly make appropriate reflected waves from the composition. : \ 90 \ 90609.DOC -18-200540450 The brightening film can not only effectively increase the brightness of the LCD display, but also can use multiple layers to effectively cover the entire visible light bandwidth, and is used in general displays that require full-spectrum white light. Or the special display driving mode applied to the special bandwidth range. The following patent application scope is used to define the reasonable protection scope of the present invention. However, it should be clear that those skilled in the art can make use of the disclosure of the present invention. The various obvious improvements should also belong to the reasonable protection scope of the present invention. [Simplified illustration of the figure] Figure 1 shows the conventional LCD (I) and the liquid crystal display (II) with a cholesteric optical film. No intention. FIG. 2 is a spectrum of the reflection band width of the cholesteric liquid crystal formulations 1 to 3 in Examples 1 to 3 of the present invention. FIG. 3 is a spectrum of the reflection band width of the cholesteric liquid crystal formulations 1 to 3 in Examples 4 to 9 of the present invention. [Simplified description of the symbols of the diagram elements] 10 Reflective plate 12 Light guide plate 14 Cholesterol liquid crystal optical film 16 λ / 4 retardation plate 18 Lower polarizer 20 Liquid crystal layer 22 Upper polarizer 24 Light source 卩 8 1 ^ ¥ \ 新 案 \ 90609 \ 90609 € 5 Changxing-FINAL.DOC -19-
Claims (1)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| TW93115597A TWI293375B (en) | 2004-06-01 | 2004-06-01 | Optical film and preparation method thereof |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| TW93115597A TWI293375B (en) | 2004-06-01 | 2004-06-01 | Optical film and preparation method thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| TW200540450A true TW200540450A (en) | 2005-12-16 |
| TWI293375B TWI293375B (en) | 2008-02-11 |
Family
ID=45067829
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| TW93115597A TWI293375B (en) | 2004-06-01 | 2004-06-01 | Optical film and preparation method thereof |
Country Status (1)
| Country | Link |
|---|---|
| TW (1) | TWI293375B (en) |
-
2004
- 2004-06-01 TW TW93115597A patent/TWI293375B/en not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| TWI293375B (en) | 2008-02-11 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| KR101436795B1 (en) | Volume photo-aligned retarder | |
| TW494258B (en) | Circularly polarized light separation plate and method of producing the same | |
| US6319963B1 (en) | Reflective film | |
| JP4801056B2 (en) | Method for producing multilayer cholesteric liquid crystal optical body | |
| JP3272668B2 (en) | Method for extending cholesteric reflection band of photopolymerizable cholesteric liquid crystal and optical element manufactured by this method | |
| CN101354459B (en) | Method for preparing liquid-crystal film material capable of reflecting circle polarized light and non-polarized light | |
| TWI547719B (en) | Optical film | |
| CN100559218C (en) | Cholesteric liquid crystal optical body and methods of making and using same | |
| EP0982605A1 (en) | Reflective film | |
| CN101710192B (en) | Preparation method of liquid crystal polarizing film with characteristic of ultra-wide wave reflection | |
| WO2004063779A1 (en) | Broad-band-cholesteric liquid-crystal film, process for producing the same, circularly polarizing plate, linearly polarizing element, illuminator, and liquid-crystal display | |
| JP2014164111A (en) | Functional film | |
| ES2258736T3 (en) | POLYMERIZABLE MIXTURES | |
| CN112592724A (en) | Method for preparing wide wave reflection film material by nano zinc oxide film diffusion method | |
| CN114656855B (en) | A preparation method and application of a broad-wave reflective flexible film material | |
| TWI518420B (en) | Method for producing liquid crystal display element and liquid crystal display element | |
| TW200946992A (en) | Low color shift polarizer assembly and the back light units, liquid crystal displays therein | |
| CN105062504B (en) | A kind of brightness enhancement film polymerizability liquid-crystal composition | |
| CN100485481C (en) | Optical film and method for producing same | |
| WO2004088366A1 (en) | Process for producing wideband cholesteric liquid crystal film, circular polarization plate, linear polarizer, lighting apparatus and liquid crystal display | |
| CN101866030B (en) | Low color shift polarizing element, low color shift polarizing light source and liquid crystal display | |
| TW200540450A (en) | Optical film and preparation method thereof | |
| KR102365610B1 (en) | Antireflection film | |
| CN105542795B (en) | Chiral polymerizable liquid crystal composition and its application | |
| Li et al. | Preparation of liquid crystal film capable of shielding visible light band by two‐phase coexistence |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Annulment or lapse of patent due to non-payment of fees |