[go: up one dir, main page]

WO2018160022A1 - Dispositif électroluminescent organique - Google Patents

Dispositif électroluminescent organique Download PDF

Info

Publication number
WO2018160022A1
WO2018160022A1 PCT/KR2018/002503 KR2018002503W WO2018160022A1 WO 2018160022 A1 WO2018160022 A1 WO 2018160022A1 KR 2018002503 W KR2018002503 W KR 2018002503W WO 2018160022 A1 WO2018160022 A1 WO 2018160022A1
Authority
WO
WIPO (PCT)
Prior art keywords
substituted
unsubstituted
alkyl
membered
arylsilyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/KR2018/002503
Other languages
English (en)
Inventor
Sang-Hee Cho
Bitnari Kim
Jeong-Eun YANG
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
DuPont Specialty Materials Korea Ltd
Original Assignee
Rohm and Haas Electronic Materials Korea Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from KR1020180023907A external-priority patent/KR102613183B1/ko
Application filed by Rohm and Haas Electronic Materials Korea Ltd filed Critical Rohm and Haas Electronic Materials Korea Ltd
Priority to CN201880010818.8A priority Critical patent/CN110268037B/zh
Priority to JP2019543951A priority patent/JP2020509584A/ja
Priority to US16/483,063 priority patent/US20200235307A1/en
Publication of WO2018160022A1 publication Critical patent/WO2018160022A1/fr
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Images

Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/56—Ring systems containing three or more rings
    • C07D209/80—[b, c]- or [b, d]-condensed
    • C07D209/94—[b, c]- or [b, d]-condensed containing carbocyclic rings other than six-membered
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/06—Peri-condensed systems
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/654—Aromatic compounds comprising a hetero atom comprising only nitrogen as heteroatom
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00—Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60—Organic compounds having low molecular weight
    • H10K85/649—Aromatic compounds comprising a hetero atom
    • H10K85/657—Polycyclic condensed heteroaromatic hydrocarbons
    • H10K85/6576—Polycyclic condensed heteroaromatic hydrocarbons comprising only sulfur in the heteroaromatic polycondensed ring system, e.g. benzothiophene
    • H—ELECTRICITY
    • H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05B—ELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B33/00—Electroluminescent light sources
    • H05B33/12—Light sources with substantially two-dimensional radiating surfaces
    • H05B33/14—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the electroluminescent material, or by the simultaneous addition of the electroluminescent material in or onto the light source
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K2101/00—Properties of the organic materials covered by group H10K85/00
    • H10K2101/10—Triplet emission
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00—Organic light-emitting devices
    • H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
    • H—ELECTRICITY
    • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00—Organic light-emitting devices
    • H10K50/10—OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/14—Carrier transporting layers
    • H10K50/16—Electron transporting layers

Definitions

  • the present disclosure relates to an organic electroluminescent device comprising a light-emitting layer and an electron transport zone.
  • An electroluminescent (EL) device is a self-light-emitting device with the advantages of providing a wider viewing angle, a greater contrast ratio, and a faster response time.
  • the first organic EL device was developed by Eastman Kodak in 1987, by using small aromatic diamine molecules and aluminum complexes as materials for forming a light-emitting layer ( see Appl. Phys. Lett. 51, 913, 1987).
  • An organic EL device changes electric energy into light by the injection of a charge into an organic light-emitting material, and commonly comprises an anode, a cathode, and an organic layer formed between the two electrodes.
  • the organic layer of the organic EL device may be composed of a hole injection layer, a hole transport layer, an electron blocking layer, a light-emitting layer (containing host and dopant materials), an electron buffer layer, a hole blocking layer, an electron transport layer, an electron injection layer, etc.; the materials used in the organic layer can be classified into a hole injection material, a hole transport material, an electron blocking material, a light-emitting material, an electron buffer material, a hole blocking material, an electron transport material, an electron injection material, etc., depending on functions.
  • the organic EL device In the organic EL device, holes from an anode and electrons from a cathode are injected into a light-emitting layer by electric voltage, and an exciton having high energy is produced by the recombination of the holes and electrons.
  • the organic light-emitting compound moves into an excited state by the energy and emits light from energy when the organic light-emitting compound returns to the ground state from the excited state.
  • the most important factor determining luminous efficiency in an organic EL device is light-emitting materials.
  • the light-emitting materials are required to have the following features: high quantum efficiency, high movement degree of an electron and a hole, and uniformality and stability of the formed light-emitting material layer.
  • the light-emitting material is classified into blue, green, and red light-emitting materials according to the light-emitting color, and further includes yellow or orange light-emitting materials. Furthermore, the light-emitting material is classified into a host material and a dopant material in a functional aspect.
  • an urgent task is the development of an organic EL device having high efficiency and long lifespan. In particular, the development of highly excellent light-emitting material over conventional materials is urgently required, considering the EL properties necessary for medium- and large-sized OLED panels.
  • an electron transport material actively transports electrons from a cathode to a light-emitting layer and inhibits transport of holes which are not recombined in the light-emitting layer to increase recombination opportunity of holes and electrons in the light-emitting layer.
  • electron-affinitive materials are used as an electron transport material.
  • Organic metal complexes having light-emitting function such as Alq 3 are excellent in transporting electrons, and thus have been conventionally used as an electron transport material.
  • Alq 3 has problems in that it moves to other layers and shows reduction of lifespan. Therefore, new electron transport materials have been required, which do not have the above problems, are highly electron-affinitive, and quickly transport electrons in organic EL devices to provide organic EL devices having high luminous efficiency.
  • the electron buffer layer is a layer for solving the problem of deterioration in luminance caused by the change of a current characteristic of the device when exposed to a high temperature during a process of producing a panel.
  • the characteristic of the compound comprised in the electron buffer layer is important.
  • the compound used in the electron buffer layer is preferable to function as to control the injection of the electrons due to the electron withdrawing property and the LUMO energy value of electron affinity, thereby enhancing the efficiency and lifespan of the organic EL device.
  • U.S. Patent No. 6,902,831 discloses an azulene derivative as an organic electroluminescent compound. However, said reference does not specifically disclose an organic electroluminescent compound of a fused azulene derivative.
  • the objective of the present disclosure is to provide an organic electroluminescent device having low voltage, high efficiency, and/or long lifespan by comprising a specific combination of a light-emitting layer and an electron transport zone.
  • a light-emitting layer comprising a phosphorescent dopant
  • the hole and electron current characteristics of the light-emitting material are excellent for low voltage, high efficiency and long lifespan, and the thermal stability of the material is excellent for improvement of lifespan.
  • using a light-emitting material having a narrow energy band gap can contribute to improve driving voltage and luminous efficiency by minimizing the charge trap.
  • the azulene derivative comprised in the device of the present disclosure has a slow transition constant of the internal conversion of S 2 ⁇ S 1 of 7*10 -8 s, the transition constant of the internal conversion of S 1 ⁇ S 0 is fast, i.e.
  • the present inventors found that by comprising the fused azulene derivative of the present disclosure in the light-emitting layer and comprising the heterocyclic derivative comprising azines of the present disclosure in the electron transport zone, it is possible to obtain fast driving voltage, high efficiency, and/or long lifespan characteristics.
  • an organic electroluminescent device comprising a first electrode; a second electrode facing the first electrode; a light-emitting layer between the first electrode and the second electrode; and an electron transport zone between the light-emitting layer and the second electrode, wherein the light-emitting layer comprises a compound represented by the following formula 1, and the electron transport zone comprises a compound represented by the following formula 11:
  • X 1 represents N-L-(Ar) a , S, or O;
  • L represents a single bond, a substituted or unsubstituted (C6-C30)arylene, or a substituted or unsubstituted (3- to 30-membered)heteroarylene;
  • Ar represents hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted mono- or di- (C1-C30)alkylamino, a substituted or unsubstituted mono- or di- (C6-C30)arylamino, or a substituted or unsubstituted (C1-C30)alkyl(C6-C30)arylamino;
  • Y 1 to Y 12 each independently represent N or CR 1 ;
  • R 1 each independently represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30)ary
  • a represents an integer of 1 to 4, where if a is an integer of 2 or more, each of Ar may be the same or different;
  • N 1 and N 2 each independently represent N or CR 18 , where at least one of N 1 and N 2 represents N;
  • Z 1 to Z 4 each independently represent N or CR 19 ;
  • R 18 and R 19 each independently represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C50)aryl, a substituted or unsubstituted (3- to 50-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (3- to 7-membered)heterocycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi
  • an organic electroluminescent device having low voltage, high efficiency, and/or long lifespan can be provided, and it is possible to produce a display device or a lighting device using the same.
  • Figure 1 illustrates a schematic sectional view of an organic electroluminescent device according to an embodiment of the present disclosure.
  • Figure 2 illustrates the molecular shape of the compound represented by formula 1 according to an embodiment of the present disclosure in a three-dimensional shape.
  • Figure 3 illustrates a current efficiency versus a luminance of organic electroluminescent devices of Comparative Example 1 and Device Example 1.
  • organic electroluminescent compound in the present disclosure means a compound that may be used in an organic electroluminescent device, and may be comprised in any material layer constituting an organic electroluminescent device, as necessary.
  • organic electroluminescent material in the present disclosure means a material that may be used in an organic electroluminescent device, and may comprise at least one compound.
  • the organic electroluminescent material may be comprised in any layer constituting an organic electroluminescent device, as necessary.
  • the organic electroluminescent material may be a hole injection material, a hole transport material, a hole auxiliary material, a light-emitting auxiliary material, an electron blocking material, a light-emitting material, an electron buffer material, a hole blocking material, an electron transport material, an electron injection material, etc.
  • the organic electroluminescent device of the present disclosure comprises a first electrode; a second electrode facing the first electrode; and a light-emitting layer between the first electrode and the second electrode, may comprise a hole transport zone between the first electrode and the light-emitting layer, and may comprise an electron transport zone between the light-emitting layer and the second electrode.
  • One of the first and second electrodes may be an anode and the other may be a cathode.
  • the hole transport zone is meant to be a zone wherein holes are transported between the first electrode and the light-emitting layer, and may comprise, for example, one or more of a hole injection layer, a hole transport layer, a hole auxiliary layer, a light-emitting auxiliary layer, and an electron blocking layer.
  • the hole injection layer, the hole transport layer, the hole auxiliary layer, the light-emitting auxiliary layer, and the electron blocking layer, respectively may be a single layer, or a multi-layer in which two or more layers are stacked.
  • the hole transport zone may comprise a p-doped hole injection layer, hole transport layer, and light-emitting auxiliary layer.
  • the p-doped hole injection layer means a hole injection layer in which a p-dopant is doped.
  • a p-dopant is a material to provide a p semiconductor characteristic.
  • a p semiconductor characteristic means a characteristic receiving or transporting holes by HOMO energy level, i.e. a characteristic of a material of high hole conductivity.
  • the light-emitting layer emits light, which may be a single layer, or a multi-layer in which two or more layers are stacked.
  • the doping concentration of the dopant compound to the host compound in the light-emitting layer is preferably less than 20 wt%.
  • the electron transport zone is meant to be a zone wherein electrons are transported between the light-emitting layer and the second electrode, and may comprise, for example, one or more of a hole blocking layer, an electron transport layer, an electron buffer layer, and an electron injection layer.
  • the hole blocking layer, the electron transport layer, the electron buffer layer, and the electron injection layer, respectively, may be a single layer, or a multi-layer in which two or more layers are stacked.
  • the light-emitting layer comprises a compound represented by formula 1
  • the electron transport zone comprises a compound represented by formula 11.
  • the electron transport zone may comprise one or more of an electron transport layer and an electron buffer layer
  • the compound represented by formula 11 may be comprised in one or more of the electron transport layer and the electron buffer layer.
  • the electron buffer layer may be comprised between the light-emitting layer and the electron transport layer, and may be comprised between the electron transport layer and the second electrode.
  • (C1-C30)alkyl is meant to be a linear or branched alkyl having 1 to 30 carbon atoms constituting the chain, in which the number of carbon atoms is preferably 1 to 10, more preferably 1 to 6, and includes methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, tert-butyl, etc.
  • (C3-C30)cycloalkyl is a mono- or polycyclic hydrocarbon having 3 to 30 ring backbone carbon atoms, in which the number of carbon atoms is preferably 3 to 20, more preferably 3 to 7, and includes cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, etc.
  • (3- to 7-membered)heterocycloalkyl is a cycloalkyl having at least one hetero atom selected from the group consisting of B, N, O, S, Si, and P, preferably O, S, and N, and 3 to 7 ring backbone atoms, and includes tetrahydrofuran, pyrrolidine, thiolan, tetrahydropyran, etc.
  • (C6-C30)aryl(ene) is a monocyclic or fused ring-type radical derived from an aromatic hydrocarbon having 6 to 30 ring backbone carbon atoms, in which the number of ring backbone carbon atoms is preferably 6 to 20, more preferably 6 to 15, may be partially saturated, and includes phenyl, biphenyl, terphenyl, naphthyl, binaphthyl, phenylnaphthyl, naphthylphenyl, fluorenyl, phenylfluorenyl, benzofluorenyl, dibenzofluorenyl, phenanthrenyl, phenylphenanthrenyl, anthracenyl, indenyl, triphenylenyl, pyrenyl, tetracenyl, perylenyl, chrysenyl, naphthacenyl, fluoranthenyl, etc.
  • (3- to 30-membered)heteroaryl(ene) is an aryl group having at least one, preferably 1 to 4 hetero atoms selected from the group consisting of B, N, O, S, Si, and P, and 3 to 30 ring backbone atoms, in which the number of ring backbone atoms is preferably 3 to 20, more preferably 5 to 15; is a monocyclic ring, or a fused ring condensed with at least one benzene ring; may be partially saturated; may be one formed by linking at least one heteroaryl or aryl group to a heteroaryl group via a single bond(s); and includes a monocyclic ring-type heteroaryl including furyl, thiophenyl, pyrrolyl, imidazolyl, pyrazolyl, thiazolyl, thiadiazolyl, isothiazolyl, isoxazolyl, oxazolyl, oxadiazolyl, triazinyl,
  • substituted in the expression “substituted or unsubstituted” means that a hydrogen atom in a certain functional group is replaced with another atom or functional group, i.e., a substituent.
  • X 1 represents N-L-(Ar) a , S, or O.
  • L represents a single bond, a substituted or unsubstituted (C6-C30)arylene, or a substituted or unsubstituted (3- to 30-membered)heteroarylene; preferably, a single bond, a substituted or unsubstituted (C6-C25)arylene, or a substituted or unsubstituted (5- to 25-membered)heteroarylene; and more preferably, a single bond, an unsubstituted (C6-C18)arylene, or an unsubstituted (5- to 18-membered)heteroarylene, wherein the heteroarylene may comprise one or more of nitrogen, oxygen, and sulfur.
  • L may represent a single bond, a substituted or unsubstituted phenylene, a substituted or unsubstituted naphthylene, a substituted or unsubstituted biphenylene, a substituted or unsubstituted pyridylene, a substituted or unsubstituted pyrimidylene, a substituted or unsubstituted triazinylene, a substituted or unsubstituted quinazolinylene, a substituted or unsubstituted quinoxalinylene, a substituted or unsubstituted naphthyridinylene, a substituted or unsubstituted benzoquinazolinylene, a substituted or unsubstituted benzothienopyrimidinylene, a substituted or unsubstituted acenaphthopyrimidinylene, a substituted or unsubstituted
  • Ar represents hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted mono- or di- (C1-C30)alkylamino, a substituted or unsubstituted mono- or di- (C6-C30)arylamino, or a substituted or unsubstituted (C1-C30)alkyl(C6-C30)arylamino; preferably, a substituted or unsubstituted (C6-C25)aryl, a substituted or unsubstituted (5- to 30-membered)heteroaryl, or a substituted or unsubstituted di(C6-C25)arylamino
  • Ar may represent a substituted or unsubstituted phenyl, a substituted or unsubstituted naphthyl, a substituted or unsubstituted biphenyl, a substituted or unsubstituted terphenyl, a substituted or unsubstituted triazinyl, a substituted or unsubstituted pyridyl, a substituted or unsubstituted pyrimidinyl, a substituted or unsubstituted quinazolinyl, a substituted or unsubstituted benzoquinazolinyl, a substituted or unsubstituted quinoxalinyl, a substituted or unsubstituted benzoquinoxalinyl, a substituted or unsubstituted quinolyl, a substituted or unsubstituted benzoquinolyl, a substituted or unsubstituted iso
  • a represents an integer of 1 to 4, preferably, 1 or 2, where if a is an integer of 2 or more, each of Ar may be the same or different.
  • Y 1 to Y 12 each independently represent N or CR 1 . According to one embodiment of the present disclosure, Y 1 to Y 12 may all represent CR 1 , and according to another embodiment of the present disclosure, at least one of Y 1 to Y 12 may represent N. Where there are a plurality of R 1 ’s, each of R 1 may be the same or different.
  • R 1 each independently represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30)ary
  • R 1 may each independently represent hydrogen, a substituted or unsubstituted methyl, a substituted or unsubstituted phenyl, a substituted or unsubstituted naphthyl, a substituted or unsubstituted biphenyl, a substituted or unsubstituted pyridyl, a substituted or unsubstituted pyrimidinyl, a substituted or unsubstituted triazinyl, a substituted or unsubstituted quinazolinyl, a substituted or unsubstituted quinoxalinyl, a substituted or unsubstituted phenylbiphenylamino, etc.
  • At least one adjacent pair of Y 1 to Y 12 in formula 1 are CR 1 , and the adjacent two R 1 ’s of CR 1 are fused together to each independently form a ring represented by any one of the following formulas 2 to 6, but is not limited thereto.
  • the formed ring may be, including the ring of formulas 2 to 6, a substituted or unsubstituted benzene ring, a naphthalene ring, a furan ring, a thiophene ring, a substituted or unsubstituted pyrrole ring, a pyridine ring, a benzofuran ring, a benzothiophene ring, a substituted or unsubstituted indole ring, a dibenzofuran ring, a dibenzothiophene ring, a substituted or unsubstituted carbazole ring, a phenanthrene ring, etc.
  • A represents N or CR 2 . According to one embodiment of the present disclosure, all A may represent CR 2 , and according to another embodiment of the present disclosure, at least one of A may represent N. Where there are a plurality of R 2 ’s, each of R 2 may be the same or different.
  • R 2 each independently represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30)ary
  • R 3 represents hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (3- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted or unsubstituted tri(C6-C30)ary
  • N 1 and N 2 each independently represent N or CR 18 , where at least one of N 1 and N 2 represents N. According to one embodiment of the present disclosure, N 1 and N 2 both represent N.
  • Z 1 to Z 4 each independently represent N or CR 19 .
  • Z 1 represents N or CR 19
  • Z 2 to Z 4 each independently represent CR 19 .
  • R 18 and R 19 each independently represent hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C50)aryl, a substituted or unsubstituted (3- to 50-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (3- to 7-membered)heterocycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyl
  • R 18 and R 19 each independently represent hydrogen, a substituted or unsubstituted (C6-C40)aryl, or a substituted or unsubstituted (5- to 45-membered)heteroaryl; or are linked to an adjacent substituent(s) to form a substituted or unsubstituted, mono- or polycyclic, (3- to 25-membered) alicyclic or aromatic ring, or the combination thereof, whose carbon atom(s) may be replaced with at least one heteroatom selected from nitrogen, oxygen, and sulfur; more preferably, hydrogen, a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (5- to 40-membered)heteroaryl; or are linked to an adjacent substituent(s) to form a substituted or unsubstituted, mono- or polycyclic, (3- to 18-membered) aromatic ring, whose carbon atom(s) may be replaced with at
  • Formula 11 may be represented by the following formula 21:
  • Z 1 is as defined in formula 11, and A 1 and A 2 are each independently identical to the definition of R 19 of formula 11, and m represents 1 or 2.
  • L 2 represents a single bond, a substituted or unsubstituted (C6-C50)arylene, or a substituted or unsubstituted (5- to 50-membered)heteroarylene; preferably, a single bond, a substituted or unsubstituted (C6-C45)arylene, or a substituted or unsubstituted (5- to 45-membered)heteroarylene; more preferably, a single bond, a substituted or unsubstituted (C6-C30)arylene, or a substituted or unsubstituted (5- to 30-membered)heteroarylene; and for example, a single bond, a phenylene unsubstituted or substituted with a pyridinyl(s), an unsubstituted naphthylene, an unsubstituted biphenylene, an unsubstituted terphenylene, an unsubstituted pheny
  • Ar 2 represents a substituted or unsubstituted (C6-C50)aryl, or a substituted or unsubstituted (5- to 50-membered)heteroaryl; preferably, a substituted or unsubstituted (C6-C45)aryl, or a substituted or unsubstituted (5- to 45-membered)heteroaryl; more preferably, a substituted or unsubstituted (C6-C30)aryl, or a substituted or unsubstituted (5- to 40-membered)heteroaryl; and for example, a phenyl unsubstituted or substituted with a pyridinyl(s), an unsubstituted naphthyl, a fluorenyl substituted with dimethyl, a fluorenyl substituted with diphenyl, a benzofluorenyl substituted with dimethyl, an unsubstituted phenanthren
  • the substituent of the substituted carbazolyl may be one or more of a fluorenyl substituted with a phenyl(s), a carbazolyl substituted with a phenyl(s), a methyl, a phenyl, a dibenzothiophenyl, and a dibenzofuranyl.
  • the substituent of the substituted (13- to 38-membered)heteroaryl may be one or more of a methyl, a tert -butyl, a phenyl, a naphthyl, and a biphenyl.
  • the ring may be a substituted or unsubstituted, mono- or polycyclic, (3- to 30-membered) alicyclic or aromatic ring, or the combination thereof, and may contain at least one heteroatom selected from nitrogen, oxygen, and sulfur.
  • the heteroaryl(ene) may each independently comprise one or more heteroatoms selected from B, N, O, S, Si, and P, and preferably selected from N, O, and S.
  • the heterocycloalkyl comprises one or more heteroatoms selected from N, O, and S.
  • the heteroatom may be bonded by one or more substituent selected from the group consisting of hydrogen, deuterium, a halogen, a cyano, a substituted or unsubstituted (C1-C30)alkyl, a substituted or unsubstituted (C6-C30)aryl, a substituted or unsubstituted (5- to 30-membered)heteroaryl, a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C1-C30)alkoxy, a substituted or unsubstituted tri(C1-C30)alkylsilyl, a substituted or unsubstituted di(C1-C30)alkyl(C6-C30)arylsilyl, a substituted or unsubstituted (C1-C30)alkyldi(C6-C30)arylsilyl, a substituted
  • the compound represented by formula 1 includes the following compounds, but is not limited thereto:
  • the compound represented by formula 11 includes the following compounds, but is not limited thereto:
  • the compound represented by formula 1 and the compound represented by formula 11 or 21 of the present disclosure can be prepared by a synthetic method known to a person skilled in the art.
  • the compound of formula 1 can be prepared by the following reaction schemes, and by referring to Korean Patent Appln. Nos. 2017-0124258 (2017.09.26), 2017-0124285 (2017.09.26), etc.
  • the compound represented by formula 11 or 21 can be prepared by referring to Korean Patent No. 1741415 (2017.05.30) and Korean Appln. Laying-Open Nos. 2015-0108332 (2015.09.25), 2015-0124886 (2015.11.06), 2015-0128590 (2015.11.18), 2016-0010333 (2016.01.27), 2016-0014556 (2016.02.11), 2016-0018406 (2016.02.17), 2016-0099471 (2016.08.22), 2017-0051198 (2017.05.11), 2017-0067643 (2017.06.16), etc.
  • the light-emitting layer of the present disclosure may be formed using a host compound and a dopant compound.
  • the host compound may be the compound represented by formula 1 alone, or any conventional material comprised in organic electroluminescent materials may be additionally comprised.
  • the dopant compound is not particularly limited, but is preferably selected from metallated complex compounds of iridium (Ir), osmium (Os), copper (Cu), and platinum (Pt), is more preferably selected from ortho-metallated complex compounds of iridium (Ir), osmium (Os), copper (Cu), and platinum (Pt), and is even more preferably an ortho-metallated iridium complex compound.
  • the dopant comprised in the organic electroluminescent device of the present disclosure may be selected from the group consisting of the compounds represented by formulas 101 to 104 below.
  • L d is selected from the following structures:
  • R 100 , R 134 , and R 135 each independently represent hydrogen, deuterium, a substituted or unsubstituted (C1-C30)alkyl, or a substituted or unsubstituted (C3-C30)cycloalkyl;
  • R 101 to R 109 and R 111 to R 123 each independently represent hydrogen, deuterium, a halogen, a (C1-C30)alkyl unsubstituted or substituted with deuterium or a halogen(s), a substituted or unsubstituted (C3-C30)cycloalkyl, a substituted or unsubstituted (C6-C30)aryl, a cyano, or a substituted or unsubstituted (C1-C30)alkoxy; adjacent substituents of R 106 to R 109 may be linked to each other to form a substituted or unsubstituted fused ring, e.g., a fluorene unsubstituted or substituted with an alkyl(s), a dibenzothiophene unsubstituted or substituted with an alkyl(s), or a dibenzofuran unsubstituted or substituted with an alkyl(s); and
  • R 124 to R 133 and R 136 to R 139 each independently represent hydrogen, deuterium, a halogen, a substituted or unsubstituted (C1-C30)alkyl, or a substituted or unsubstituted (C6-C30)aryl; and adjacent substituents of R 124 to R 127 may be linked to each other to form a substituted or unsubstituted fused ring, e.g., a fluorene unsubstituted or substituted with an alkyl(s), a dibenzothiophene unsubstituted or substituted with an alkyl(s), or a dibenzofuran unsubstituted or substituted with an alkyl(s);
  • X represents CR 21 R 22 , O, or S
  • R 21 and R 22 each independently represent a substituted or unsubstituted (C1-C10)alkyl, or a substituted or unsubstituted (C6-C30)aryl;
  • R 201 to R 211 each independently represent hydrogen, deuterium, a halogen, a (C1-C30)alkyl unsubstituted or substituted with deuterium or a halogen(s), a substituted or unsubstituted (C3-C30)cycloalkyl, or a (C6-C30)aryl unsubstituted or substituted with an alkyl(s) or deuterium; and adjacent substituents of R 208 to R 211 may be linked to each other to form a substituted or unsubstituted fused ring, e.g., a fluorene unsubstituted or substituted with an alkyl(s), a dibenzothiophene unsubstituted or substituted with an alkyl(s), or a dibenzofuran unsubstituted or substituted with an alkyl(s);
  • each R 100 may be the same or different;
  • n an integer of 1 to 3.
  • the specific examples of the dopant compound are as follows.
  • Figure 1 illustrates a schematic sectional view of an organic electroluminescent device according to an embodiment of the present disclosure.
  • Figure 1 shows an organic electroluminescent device 100 comprising a substrate 101, a first electrode 110 formed on the substrate 101, an organic layer 120 formed on the first electrode 110, and a second electrode 130 formed on the organic layer 120 and facing the first electrode 110.
  • the organic layer 120 comprises a hole injection layer 122, a hole transport layer 123 formed on the hole injection layer 122, a light-emitting layer 125 formed on the hole transport layer 123, and an electron transport zone 129 formed on the light-emitting layer 125; and the electron transport zone 129 comprises an electron buffer layer 126 formed on the light-emitting layer 125, an electron transport layer 127 formed on the electron buffer layer 126, and an electron injection layer 128 formed on the electron transport layer 127.
  • the light-emitting layer 125 may be prepared with a host compound and a dopant compound.
  • the kinds of host compound and dopant compound to be used are not particularly limited, and may be selected from compounds known in the art.
  • the examples of the host compound and the dopant compound are as described above.
  • the dopant can be doped in an amount of less than about 25 wt%, and preferably less than 17 wt%, based on the total amount of the dopant and host of the light-emitting layer.
  • the light emitting layer 125 is composed of two or more layers, each of the layers may be prepared to emit a color different from one another.
  • the device may emit white light by preparing three light-emitting layers 125 which emit blue, red, and green colors, respectively.
  • the device may include light-emitting layers which emit yellow or orange color, if necessary.
  • the electron transport zone 129 means a zone in which electrons are transported from the second electrode to the light-emitting layer.
  • the electron transport zone 129 can comprise an electron transport compound, a reductive dopant, or a combination thereof.
  • the electron transport compound can be at least one selected from the group consisting of phenanthrene-based compounds, oxazole-based compounds, isoxazole-based compounds, triazole-based compounds, isothiazole-based compounds, oxadiazole-based compounds, thiadiazole-based compounds, perylene-based compounds, anthracene-based compounds, aluminum complexes, and gallium complexes.
  • the reductve dopant may be selected from the group consisting of alkali metals, alkali metal compounds, alkaline earth metals, rare-earth metals, and halides, oxides, and complexes thereof.
  • the reductive dopant includes lithium quinolate, sodium quinolate, cesium quinolate, potassium quinolate, LiF, NaCl, CsF, Li 2 O, BaO, and BaF 2 , but is not limited thereto.
  • the electron transport zone 129 can comprise an electron buffer layer 126, an electron transport layer 127, and/or an electron injection layer 128.
  • the thickness of the electron buffer layer 126 is 1 nm or more, but is not particularly limited thereto. Specifically, the thickness of the electron buffer layer 126 may be in the range of from 2 nm to 200 nm.
  • the electron buffer layer 126 may be formed on the light-emitting layer 125 by using known various methods such as vacuum deposition, wet film-forming methods, laser induced thermal imaging, etc.
  • the electron buffer layer indicates a layer controlling an electron flow. Therefore, the electron buffer layer may be, for example, a layer which traps electrons, blocks electrons, or lowers an energy barrier between an electron transport zone and a light-emitting layer.
  • the electron buffer layer 126 may be comprised in an organic electroluminescent device emitting all kinds of colors, i.e. blue, red, green, etc.
  • the electron transport layer 127 and the electron injection layer 128 can each be composed of two or more layers.
  • the electron injection layer 128 may be prepared with any electron injection material known in the art, which includes lithium quinolate, sodium quinolate, cesium quinolate, potassium quinolate, LiF, NaCl, CsF, Li 2 O, BaO, and BaF 2 , but is not limited thereto.
  • the aforementioned description regarding the organic electroluminescent device shown in Figure 1 is intended to explain one embodiment of the disclosure, and is not meant in any way to restrict the scope of the disclosure.
  • the organic electroluminescent device can be constructed in another way.
  • any one optional component such as a hole injection layer may not be comprised in the organic electroluminescent device of Figure 1, except for a light-emitting layer and an electron transport zone.
  • an optional component may be further comprised therein, which includes one or more of an impurity layer such as n-doping layer and p-doping layer.
  • the organic electroluminescent device may be a both side emission type in which a light-emitting layer is placed on each of both sides of the impurity layer.
  • the two light-emitting layers on the impurity layer may emit different colors.
  • the organic electroluminescent device may be a bottom emission type in which a first electrode is a transparent electrode and a second electrode is a reflective electrode.
  • the organic electroluminescent device may be a top emission type in which a first electrode is a reflective electrode and a second electrode is a transparent electrode.
  • the organic electroluminescent device may have an inverted type structure in which a cathode, an electron transport layer, a light-emitting layer, a hole transport layer, a hole injection layer, and an anode are sequentially stacked on a substrate.
  • the electron buffer layer of the present disclosure may comprise an electron buffer material comprising a compound represented by formula 11, or another electron buffer compound.
  • the electron transport zone of the present disclosure may comprise a compound represented by formula 11, an electron transport compound, a reductive dopant, or a combination thereof.
  • the electron transport layer of the present disclosure may comprise an electron transport material comprising a compound represented by formula 11 of the present disclosure.
  • the electron transport layer may comprise the aforementioned reductive dopant.
  • a known electron injection material may be used for the material used in the electron injection layer, which includes lithium quinolate, sodium quinolate, cesium quinolate, potassium quinolate, LiF, NaCl, CsF, Li 2 O, BaO, and BaF 2 , but is not limited thereto.
  • LUMO energy level (A) and HOMO energy level are expressed in absolute values in the present disclosure.
  • the values of the LUMO energy level are compared based on absolute values. Values calculated by density functional theory (DFT) are used for LUMO energy levels and HOMO energy levels in the present disclosure.
  • DFT density functional theory
  • the LUMO energy levels can be easily measured by known various methods. Generally, LUMO energy levels are measured by cyclic voltammetry or ultraviolet photoelectron spectroscopy (UPS). Therefore, a person skilled in the art can easily comprehend the electron buffer layer, light-emitting layer, and electron transport layer that satisfy the equational relationship of the LUMO energy levels of the present disclosure, and practice the present disclosure. HOMO energy levels can be easily measured by the same method of measuring LUMO energy levels.
  • the LUMO energy value of the light-emitting layer (Ah) and the LUMO energy value of the electron transport zone (Ae) satisfy the following equation (1).
  • Ae means the LUMO energy value of the electron transport zone comprising an electron transport layer and/or an electron buffer layer.
  • results according to the relationship of the LUMO energy values of the electron transport zone (Ae) and the light-emitting layer (Ah) are for explaining the rough tendency of the device in accordance with the overall LUMO energy groups, and so results other than the above can appear according to the inherent property of the specific derivatives, and the stability of the materials.
  • a light-emitting layer comprising a generally commercialized compound having a structure of a substituted carbazole or a fused carbazole
  • materials of fast electron current characteristic are required for low driving voltage in order to increase efficiency and improve power consumption.
  • azines of a heterocyclic derivative are generally used.
  • the electron current characteristic within the device is relatively strong which leads to exciton quenching or triplet-polaron quenching since the excitons produced in the organic electroluminescent device are extremely formed between the hole transport zone and the light-emitting layer. Accordingly, efficiency and lifespan need to be improved.
  • N ext external quantum efficiency of an organic electroluminescent device means the number of photons emitted outside compared to the number of charges injected, and the definition is as follows:
  • N ext is the external quantum efficiency
  • N int is the internal quantum efficiency
  • N out is the emission rate outside the device of the internally produced light.
  • ⁇ is the combining rate of holes and electrons
  • N ex is a producing rate of the excitons
  • ⁇ p is the PL quantum efficiency.
  • the charge-balance factor which corresponds to ⁇
  • the insufficient hole current characteristic is compensated by an appropriate charge balance through the first host compound and the factor corresponding to ⁇ is improved, which may contribute to an enhancement of the organic electroluminescent device performance.
  • the interfacial characteristic is improved by releasing the excitons extremely formed between the hole transport zone and the light-emitting layer to the light emitting layer/electron transport zone.
  • the fused azulene derivative corresponding to formula 1 of the present disclosure which has a molecular shape having suitable rigidity, has a dihedral angle of about 15°. While a perfectly planar structure can induce crystallization due to aggregation, if intermolecular stacking is appropriately conducted, long lifespan as well as fast current characteristic is possible. Therefore, by using together with a particular structure of a derivative of triazine, quinazoline, quinoxaline, pyrimidine, etc., as a host material, a luminescent device of relatively low driving voltage, excellent luminous efficiency such as current efficiency and power efficiency, and capable of realizing high color purity may be provided.
  • an azine-type heterocyclic derivative of high electron affinity as an electron transport zone material in the electron transport zone for low driving voltage
  • the electron injection becomes more easier, which may improve the driving voltage, efficiency, and lifespan of the device.
  • an azulene compound corresponding to formula 1 of the present disclosure as a host material and an azine-type material having strong electron current characteristic as an electron transport material as a combination
  • an organic electroluminescent device of high efficiency and/or long lifespan as well as low driving voltage may be provided.
  • An OLED device not according to the present disclosure was produced as follows: A transparent electrode indium tin oxide (ITO) thin film (10 ⁇ /sq) on a glass substrate for an OLED (GEOMATEC CO., LTD., Japan) was subjected to an ultrasonic washing with acetone and isopropyl alcohol, sequentially, and then was stored in isopropanol. Next, the ITO substrate was mounted on a substrate holder of a vacuum vapor deposition apparatus. Compound HI-1 was introduced into a cell of the vacuum vapor deposition apparatus, and the pressure in the chamber of the apparatus was then controlled to 10 -7 torr.
  • ITO indium tin oxide
  • Compound HT-2 was then introduced into another cell of the vacuum vapor deposition apparatus, and an electric current was applied to the cell to evaporate the introduced material, thereby forming a second hole transport layer having a thickness of 60 nm on the first hole transport layer.
  • a light-emitting layer was then deposited as follows.
  • Compound CBP as a host was introduced into one cell of the vacuum vapor deposition apparatus and compound D-71 as a dopant was introduced into another cell of the apparatus.
  • the two materials were evaporated at a different rate and the dopant was deposited in a doping amount of 3 wt%, based on the total weight of the host and dopant, to form a light-emitting layer having a thickness of 40 nm on the second hole transport layer.
  • compound B-103 and compound ETL-1 were evaporated in a weight ratio of 50:50 as electron transport materials to form an electron transport layer having a thickness of 35 nm on the light-emitting layer.
  • an Al cathode having a thickness of 80 nm was deposited by another vacuum vapor deposition apparatus on the electron injection layer.
  • All the materials used for producing the OLED device were purified by vacuum sublimation at 10 -6 torr.
  • An OLED device was produced in the same manner as in Comparative Example 1, except that compounds of Table 1 below were used as an electron transport material instead of compound B-103 .
  • An OLED device was produced in the same manner as in Comparative Example 1, except that compound B-7 was used as a host material instead of compound CBP .
  • An OLED device was produced in the same manner as in Comparative Example 7, except that compounds of Table 1 below were used as an electron transport material instead of compound B-103 .
  • an OLED device was produced in the same manner as in Comparative Example 1, except that compound CBP was used as a host material and compounds of Table 1 below were used as an electron transport material.
  • the driving voltage, luminous efficiency, CIE color coordinates, and the time period for the luminance to decrease from 100% to 95% (lifespan; T95) at a luminance of 5,000 nits of the organic electroluminescent devices produced in Comparative Examples 1 to 12 and Device Examples 1 to 6 are provided in Table 1 below.
  • a current efficiency versus a luminance of the organic electroluminescent devices of Comparative Example 1 and Device Example 1 is illustrated in Figure 3.
  • An OLED device was produced in the same manner as in Device Example 1, except that compound HT-3 of Table 4 below was evaporated as a second hole transport layer, the electron buffer material of Table 2 below was evaporated as an electron buffer layer on the light emitting layer in a thickness of 5 nm, and Alq3 was evaporated as an electron transport material on the electron buffer layer in a thickness of 30 nm.
  • an OLED device was produced in the same manner as in Comparative Example 13, except that the compounds of Table 2 below were evaporated in a weight ratio of 50:50 as electron transport materials on the electron buffer layer in a thickness of 30 nm.
  • the driving voltage, luminous efficiency, CIE color coordinates at a luminance of 1,000 nits, and the time period for the luminance to decrease from 100% to 95% (lifespan; T95) at a luminance of 5,000 nits of the organic electroluminescent devices produced in Comparative Example 13 and Device Examples 7 to 11 are provided in Table 2 below.
  • an OLED device was produced in the same manner as in Comparative Example 1, except that compound HT-4 of Table 4 below was evaporated as a second hole transport layer, and using compound C-246 as a host material and the compounds of Table 3 instead of compound B-103 as electron transport materials.
  • the driving voltage, luminous efficiency, CIE color coordinates at a luminance of 1,000 nits, and the time period for the luminance to decrease from 100% to 95% (lifespan; T95) at a luminance of 5,000 nits of the organic electroluminescent devices produced in Device Examples 12 to 16 are provided in Table 3 below.
  • organic electroluminescent device comprising the specific combination of compounds of the present disclosure is considered to be suitably applied to flexible displays, lightings, and vehicle displays which require long lifespan.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Electroluminescent Light Sources (AREA)

Abstract

La présente invention concerne un dispositif électroluminescent organique. Le dispositif électroluminescent organique de la présente invention comprend une combinaison spécifique d'une couche électroluminescente et d'une zone de transport d'électrons, offrant ainsi une faible tension, une efficacité élevée et/ou une longue durée de vie.
PCT/KR2018/002503 2017-02-28 2018-02-28 Dispositif électroluminescent organique Ceased WO2018160022A1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
CN201880010818.8A CN110268037B (zh) 2017-02-28 2018-02-28 有机电致发光装置
JP2019543951A JP2020509584A (ja) 2017-02-28 2018-02-28 有機エレクトロルミネッセンスデバイス
US16/483,063 US20200235307A1 (en) 2017-02-28 2018-02-28 Organic electroluminescent device

Applications Claiming Priority (12)

Application Number Priority Date Filing Date Title
KR10-2017-0026014 2017-02-28
KR20170026014 2017-02-28
KR20170124285 2017-09-26
KR20170124258 2017-09-26
KR10-2017-0124285 2017-09-26
KR10-2017-0124258 2017-09-26
KR20170145972 2017-11-03
KR10-2017-0145972 2017-11-03
KR10-2017-0180988 2017-12-27
KR20170180988 2017-12-27
KR10-2018-0023907 2018-02-27
KR1020180023907A KR102613183B1 (ko) 2017-02-28 2018-02-27 유기 전계 발광 소자

Publications (1)

Publication Number Publication Date
WO2018160022A1 true WO2018160022A1 (fr) 2018-09-07

Family

ID=63371030

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/KR2018/002503 Ceased WO2018160022A1 (fr) 2017-02-28 2018-02-28 Dispositif électroluminescent organique

Country Status (1)

Country Link
WO (1) WO2018160022A1 (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN112174980A (zh) * 2020-10-29 2021-01-05 烟台九目化学股份有限公司 一种以八元环为核心结构的有机化合物及其应用
CN112661752A (zh) * 2020-12-23 2021-04-16 吉林奥来德光电材料股份有限公司 菲并咪唑稠环类化合物及其制备方法和有机电致发光器件
CN113178527A (zh) * 2021-04-27 2021-07-27 京东方科技集团股份有限公司 有机电致发光器件及显示装置
CN116745296A (zh) * 2021-01-13 2023-09-12 浙江光昊光电科技有限公司 一种有机化合物、组合物及其在有机电子器件中的应用
US12082496B2 (en) 2018-03-27 2024-09-03 Rohm And Haas Electronic Materials Korea Ltd. Composition material for organic electroluminescent device, plurality of host materials, and organic electroluminescent device comprising the same

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20150121337A (ko) * 2014-04-18 2015-10-29 덕산네오룩스 주식회사 유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치
WO2016080791A1 (fr) * 2014-11-20 2016-05-26 Rohm And Haas Electronic Materials Korea Ltd. Matériaux hôtes multiples et dispositif électroluminescent organique les comprenant
WO2018021841A1 (fr) * 2016-07-27 2018-02-01 Rohm And Haas Electronic Materials Korea Ltd. Composé électroluminescent organique et dispositif électroluminescent organique le comprenant

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20150121337A (ko) * 2014-04-18 2015-10-29 덕산네오룩스 주식회사 유기전기 소자용 화합물, 이를 이용한 유기전기소자 및 그 전자 장치
WO2016080791A1 (fr) * 2014-11-20 2016-05-26 Rohm And Haas Electronic Materials Korea Ltd. Matériaux hôtes multiples et dispositif électroluminescent organique les comprenant
WO2018021841A1 (fr) * 2016-07-27 2018-02-01 Rohm And Haas Electronic Materials Korea Ltd. Composé électroluminescent organique et dispositif électroluminescent organique le comprenant

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
CALUS, S. ET AL.: "Optical absorption and fluorescence spectra of novel annulated analogues of azafluoranthene and azulene dyes", MATERIALS CHEMISTRY AND PHYSICS, vol. 121, 2010, pages 477 - 483, XP026990654 *
GASIORSKI, P ET AL.: "From pirazoloquinolines to annulated azulene dyes: UV-VIS spectroscopy and quantum chemical study", JOURNAL OF LUMINESCENCE, vol. 130, 2010, pages 2460 - 2468, XP027407571 *
SZLACHCIC, P. ET AL.: "Organic light emitting diodes (OLED) based on helical structures containing 7-membered fused rings", DYES AND PIGMENTS, vol. 114, 2015, pages 184 - 195, XP055538377 *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US12082496B2 (en) 2018-03-27 2024-09-03 Rohm And Haas Electronic Materials Korea Ltd. Composition material for organic electroluminescent device, plurality of host materials, and organic electroluminescent device comprising the same
CN112174980A (zh) * 2020-10-29 2021-01-05 烟台九目化学股份有限公司 一种以八元环为核心结构的有机化合物及其应用
CN112661752A (zh) * 2020-12-23 2021-04-16 吉林奥来德光电材料股份有限公司 菲并咪唑稠环类化合物及其制备方法和有机电致发光器件
CN116745296A (zh) * 2021-01-13 2023-09-12 浙江光昊光电科技有限公司 一种有机化合物、组合物及其在有机电子器件中的应用
CN113178527A (zh) * 2021-04-27 2021-07-27 京东方科技集团股份有限公司 有机电致发光器件及显示装置

Similar Documents

Publication Publication Date Title
WO2018105888A1 (fr) Composé électroluminescent organique et dispositif électroluminescent organique le comprenant
EP3131879A1 (fr) Matériau hôte à plusieurs constituants et dispositif électroluminescent organique comprenant ledit matériau
WO2016080791A1 (fr) Matériaux hôtes multiples et dispositif électroluminescent organique les comprenant
WO2015167259A1 (fr) Matière hôte à constituants multiples et dispositif électroluminescent organique la comprenant
WO2015178732A1 (fr) Matériau hôte multi-composant et dispositif électroluminescent organique le contenant
EP3494117A1 (fr) Composé électroluminescent organique et dispositif électroluminescent organique le comprenant
EP3129446A1 (fr) Matériau hôte à plusieurs composants et dispositif électroluminescent organique le comprenant
WO2015156587A1 (fr) Matériau hôte à plusieurs composants et dispositif électroluminescent organique le comprenant
EP3170206A1 (fr) Dispositif électroluminescent organique
WO2016076629A1 (fr) Pluralité de matériaux hôtes et dispositif électroluminescent organique comprenant ces matériaux
WO2018021841A1 (fr) Composé électroluminescent organique et dispositif électroluminescent organique le comprenant
EP3119751A1 (fr) Matériau tampon d'électrons et dispositif électroluminescent organique
EP3172780A1 (fr) Dispositif électroluminescent organique
EP3446345A1 (fr) Pluralité de matériaux hôtes et dispositif électroluminescent organique les comprenant
WO2016013875A1 (fr) Dispositif électroluminescent organique
EP3371182A1 (fr) Matériaux tampon d'électrons, matériaux de transport d'électrons et dispositif électroluminescent organique les comprenant
WO2015142040A1 (fr) Matériau tampon d'électrons et dispositif électroluminescent organique
WO2016013867A1 (fr) Dispositif électroluminescent organique
WO2015099507A1 (fr) Nouveau composé organique électroluminescent, matériau hôte à plusieurs constituants et dispositif organique électroluminescent le comprenant
WO2017183859A1 (fr) Pluralité de matériaux hôtes et dispositif électroluminescent organique les comprenant
WO2018230969A1 (fr) Composé organique et élément électroluminescent organique le comprenant
WO2014129846A1 (fr) Composés électroluminescents organiques et dispositif électroluminescent organique comprenant ces composés
EP3313958A1 (fr) Matériau hôte multicomposant et dispositif électroluminescent organique comprenant ce matériau
WO2015174738A1 (fr) Matériau hôte à constituants multiples et dispositif électroluminescent organique le comprenant
WO2018160022A1 (fr) Dispositif électroluminescent organique

Legal Events

Date Code Title Description
ENP Entry into the national phase

Ref document number: 2019543951

Country of ref document: JP

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 18761825

Country of ref document: EP

Kind code of ref document: A1