KR102040535B1 - 발광 소자 재료 및 발광 소자 - Google Patents
발광 소자 재료 및 발광 소자 Download PDFInfo
- Publication number
- KR102040535B1 KR102040535B1 KR1020147006015A KR20147006015A KR102040535B1 KR 102040535 B1 KR102040535 B1 KR 102040535B1 KR 1020147006015 A KR1020147006015 A KR 1020147006015A KR 20147006015 A KR20147006015 A KR 20147006015A KR 102040535 B1 KR102040535 B1 KR 102040535B1
- Authority
- KR
- South Korea
- Prior art keywords
- group
- light emitting
- substituted
- unsubstituted
- electron
- Prior art date
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- 0 CCC12IC1(*)c(ccc1c3[o]c4c1cccc4)c3N1C=CN[C@@]21 Chemical compound CCC12IC1(*)c(ccc1c3[o]c4c1cccc4)c3N1C=CN[C@@]21 0.000 description 4
- HYGLETVERPVXOS-UHFFFAOYSA-N Brc1c(ccc2c3c(cc4)ccc2)c3c4cc1 Chemical compound Brc1c(ccc2c3c(cc4)ccc2)c3c4cc1 HYGLETVERPVXOS-UHFFFAOYSA-N 0.000 description 1
- XOOKCHMUACXJNL-UHFFFAOYSA-N CB[n]1nccc1 Chemical compound CB[n]1nccc1 XOOKCHMUACXJNL-UHFFFAOYSA-N 0.000 description 1
- ZKOYFCWKRYBWSR-UHFFFAOYSA-N Cc1c(C2N(C)C=CC=C2)c(F)cc(F)c1 Chemical compound Cc1c(C2N(C)C=CC=C2)c(F)cc(F)c1 ZKOYFCWKRYBWSR-UHFFFAOYSA-N 0.000 description 1
- DZRJELAKNNROSZ-UHFFFAOYSA-N Cc1ccccc1-c1[n-]c(cccc2)c2[s]1 Chemical compound Cc1ccccc1-c1[n-]c(cccc2)c2[s]1 DZRJELAKNNROSZ-UHFFFAOYSA-N 0.000 description 1
- XDLZISCWUJCDBN-UHFFFAOYSA-N Clc1cc(-c(cc2)c(cc3)c4c2ccc2c4c3ccc2-c2cccnc2)cc(Cl)c1 Chemical compound Clc1cc(-c(cc2)c(cc3)c4c2ccc2c4c3ccc2-c2cccnc2)cc(Cl)c1 XDLZISCWUJCDBN-UHFFFAOYSA-N 0.000 description 1
- XDPHZNQRZOZLNR-UHFFFAOYSA-N Clc1cc(-c2c(ccc3cccc(cc4)c33)c3c4cc2)cc(Cl)c1 Chemical compound Clc1cc(-c2c(ccc3cccc(cc4)c33)c3c4cc2)cc(Cl)c1 XDPHZNQRZOZLNR-UHFFFAOYSA-N 0.000 description 1
- BDTUUCAAJYKILN-UHFFFAOYSA-N Clc1cc(-c2ccc(cc3)c4c2ccc2c4c3c(Cc3cccnc3)cc2)cc(Cl)c1 Chemical compound Clc1cc(-c2ccc(cc3)c4c2ccc2c4c3c(Cc3cccnc3)cc2)cc(Cl)c1 BDTUUCAAJYKILN-UHFFFAOYSA-N 0.000 description 1
- GBBCYZIDUCEVIH-UHFFFAOYSA-N Clc1cc(-c2ccc(cc3)c4c2ccc2c4c3ccc2-c2cnccc2)cc(Cl)c1 Chemical compound Clc1cc(-c2ccc(cc3)c4c2ccc2c4c3ccc2-c2cnccc2)cc(Cl)c1 GBBCYZIDUCEVIH-UHFFFAOYSA-N 0.000 description 1
- VCMDSOQEVBQGRH-UHFFFAOYSA-N c(cc1)cc2c1[o]c(-c(cc1)c(cc3)c4c1ccc1c4c3ccc1-c1cc(-c3ccccn3)cc(-c3ncccc3)c1)n2 Chemical compound c(cc1)cc2c1[o]c(-c(cc1)c(cc3)c4c1ccc1c4c3ccc1-c1cc(-c3ccccn3)cc(-c3ncccc3)c1)n2 VCMDSOQEVBQGRH-UHFFFAOYSA-N 0.000 description 1
- ATELQSPYPHTQHE-UHFFFAOYSA-N c(cc1)cc2c1[o]c(-c(cc1)c(cc3)c4c1ccc1c4c3ccc1-c1cc(-c3ccncc3)cc(-c3ccncc3)c1)n2 Chemical compound c(cc1)cc2c1[o]c(-c(cc1)c(cc3)c4c1ccc1c4c3ccc1-c1cc(-c3ccncc3)cc(-c3ccncc3)c1)n2 ATELQSPYPHTQHE-UHFFFAOYSA-N 0.000 description 1
- JHQRRRAEDIKRRG-UHFFFAOYSA-N c(cc1)cc2c1[o]c(-c1cc(-c3ccc(cc4)c5c3ccc(cc3)c5c4c3-c3cccnc3)cc(-c3nc4ccccc4[o]3)c1)n2 Chemical compound c(cc1)cc2c1[o]c(-c1cc(-c3ccc(cc4)c5c3ccc(cc3)c5c4c3-c3cccnc3)cc(-c3nc4ccccc4[o]3)c1)n2 JHQRRRAEDIKRRG-UHFFFAOYSA-N 0.000 description 1
- IRKVMZKLPPUQTI-UHFFFAOYSA-N c(cc1)cc2c1[o]c(-c1cc(-c3ccc(cc4)c5c3ccc(cc3)c5c4c3-c3nc(cccc4)c4[o]3)cc(-c3nc(cccc4)c4[o]3)c1)n2 Chemical compound c(cc1)cc2c1[o]c(-c1cc(-c3ccc(cc4)c5c3ccc(cc3)c5c4c3-c3nc(cccc4)c4[o]3)cc(-c3nc(cccc4)c4[o]3)c1)n2 IRKVMZKLPPUQTI-UHFFFAOYSA-N 0.000 description 1
- GNDFMCXNXAJGSA-UHFFFAOYSA-N c(cc1)cc2c1[s]c(-c1cc(-c3ccc(cc4)c5c3ccc(cc3)c5c4c3-c3cnccc3)cc(-c3nc4ccccc4[s]3)c1)n2 Chemical compound c(cc1)cc2c1[s]c(-c1cc(-c3ccc(cc4)c5c3ccc(cc3)c5c4c3-c3cnccc3)cc(-c3nc4ccccc4[s]3)c1)n2 GNDFMCXNXAJGSA-UHFFFAOYSA-N 0.000 description 1
- XHDUDEUVAYQRNE-UHFFFAOYSA-N c(cc1)cc2c1c(-c(cc1)ccc1-c1cc(-c3cc4cccc(-c(cc5)ccc5-c5ccc(cc6)c7c5ccc(cc5)c7c6c5-c5cc(cccc6)c6nc5)c4cn3)c(cc3)c4c1ccc(cc1)c4c3c1-c1cc(cccc3)c3nc1)cnc2 Chemical compound c(cc1)cc2c1c(-c(cc1)ccc1-c1cc(-c3cc4cccc(-c(cc5)ccc5-c5ccc(cc6)c7c5ccc(cc5)c7c6c5-c5cc(cccc6)c6nc5)c4cn3)c(cc3)c4c1ccc(cc1)c4c3c1-c1cc(cccc3)c3nc1)cnc2 XHDUDEUVAYQRNE-UHFFFAOYSA-N 0.000 description 1
- CWDCZBBIQARIFT-UHFFFAOYSA-N c(cc1)cc2c1ncc(-c(cc1)c(ccc(cc3)c45)c4c1ccc5c3-c(cc1)ccc1-c1cc3cccnc3cc1)c2 Chemical compound c(cc1)cc2c1ncc(-c(cc1)c(ccc(cc3)c45)c4c1ccc5c3-c(cc1)ccc1-c1cc3cccnc3cc1)c2 CWDCZBBIQARIFT-UHFFFAOYSA-N 0.000 description 1
- KSHQLDLCVFABMY-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(-c(cc2)c(cc3)c4c2ccc2c4c3ccc2-c2cc(-c3cccnc3)cc(-c3cnccc3)c2)nc2c1cccc2 Chemical compound c(cc1)ccc1-[n]1c(-c(cc2)c(cc3)c4c2ccc2c4c3ccc2-c2cc(-c3cccnc3)cc(-c3cnccc3)c2)nc2c1cccc2 KSHQLDLCVFABMY-UHFFFAOYSA-N 0.000 description 1
- NCCDTGMEZRRULP-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(-c(cc2)c(cc3)c4c2ccc2c4c3ccc2-c2cc(-c3ccncc3)cc(-c3ccncc3)c2)nc2c1cccc2 Chemical compound c(cc1)ccc1-[n]1c(-c(cc2)c(cc3)c4c2ccc2c4c3ccc2-c2cc(-c3ccncc3)cc(-c3ccncc3)c2)nc2c1cccc2 NCCDTGMEZRRULP-UHFFFAOYSA-N 0.000 description 1
- KIRYCBCLDYNXGM-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(-c2cc(-c3ccc(cc4)c5c3ccc(cc3)c5c4c3-c3cccnc3)cc(-c3nc4ccccc4[n]3-c3ccccc3)c2)nc2c1cccc2 Chemical compound c(cc1)ccc1-[n]1c(-c2cc(-c3ccc(cc4)c5c3ccc(cc3)c5c4c3-c3cccnc3)cc(-c3nc4ccccc4[n]3-c3ccccc3)c2)nc2c1cccc2 KIRYCBCLDYNXGM-UHFFFAOYSA-N 0.000 description 1
- BKEKRWVTQKYTQX-UHFFFAOYSA-N c(cc1)ccc1-[n]1c(-c2cc(-c3ccc(cc4)c5c3ccc(cc3)c5c4c3-c3nc(cccc4)c4[n]3-c3ccccc3)cc(-c3nc4ccccc4[n]3-c3ccccc3)c2)nc2c1cccc2 Chemical compound c(cc1)ccc1-[n]1c(-c2cc(-c3ccc(cc4)c5c3ccc(cc3)c5c4c3-c3nc(cccc4)c4[n]3-c3ccccc3)cc(-c3nc4ccccc4[n]3-c3ccccc3)c2)nc2c1cccc2 BKEKRWVTQKYTQX-UHFFFAOYSA-N 0.000 description 1
- XAAXJINYBBDIGO-UHFFFAOYSA-N c(cc1-c(cc2)ccc2-c2ccc(cc3)c4c2ccc(cc2)c4c3c2-c(cc2)ccc2-c2cccc3c2ccc(-c2ccnc(-c(cc4)ccc4-c(cc4)ccc4-c4ccc(cc5)c6c4ccc(cc4)c6c5c4-c4cccnc4)c2)n3)cc2c1nccc2 Chemical compound c(cc1-c(cc2)ccc2-c2ccc(cc3)c4c2ccc(cc2)c4c3c2-c(cc2)ccc2-c2cccc3c2ccc(-c2ccnc(-c(cc4)ccc4-c(cc4)ccc4-c4ccc(cc5)c6c4ccc(cc4)c6c5c4-c4cccnc4)c2)n3)cc2c1nccc2 XAAXJINYBBDIGO-UHFFFAOYSA-N 0.000 description 1
- WOQTZVPCRQAEER-UHFFFAOYSA-N c1c[o]c(-c2cc(-c3ncc[o]3)cc(-c3ccc(cc4)c5c3ccc(cc3)c5c4c3-c3cccnc3)c2)n1 Chemical compound c1c[o]c(-c2cc(-c3ncc[o]3)cc(-c3ccc(cc4)c5c3ccc(cc3)c5c4c3-c3cccnc3)c2)n1 WOQTZVPCRQAEER-UHFFFAOYSA-N 0.000 description 1
- XXIFEXZFDGTVSC-UHFFFAOYSA-N c1cc(-c2cc3cccnc3cc2)cc(-c2ccc(cc3)c4c2ccc(cc2)c4c3c2-c(cc2)cc3c2nccc3)c1 Chemical compound c1cc(-c2cc3cccnc3cc2)cc(-c2ccc(cc3)c4c2ccc(cc2)c4c3c2-c(cc2)cc3c2nccc3)c1 XXIFEXZFDGTVSC-UHFFFAOYSA-N 0.000 description 1
- LWJHRBHBQWAORF-UHFFFAOYSA-N c1cc(-c2ccc(cc3)c4c2ccc(cc2)c4c3c2-c(cc2)ccc2-c2cc3cccnc3cc2)c(ccnc2)c2c1 Chemical compound c1cc(-c2ccc(cc3)c4c2ccc(cc2)c4c3c2-c(cc2)ccc2-c2cc3cccnc3cc2)c(ccnc2)c2c1 LWJHRBHBQWAORF-UHFFFAOYSA-N 0.000 description 1
- PFFRSVXDASJARC-UHFFFAOYSA-N c1cc2cc(-c3cc(-c4ccc(cc5)c6c4ccc(cc4)c6c5c4-c(cc4)cc5c4nccc5)ccc3)cnc2cc1 Chemical compound c1cc2cc(-c3cc(-c4ccc(cc5)c6c4ccc(cc4)c6c5c4-c(cc4)cc5c4nccc5)ccc3)cnc2cc1 PFFRSVXDASJARC-UHFFFAOYSA-N 0.000 description 1
- JVBREHJIOZZCRX-UHFFFAOYSA-N c1cc2cncc(-c3ccc(cc4)c5c3ccc(cc3)c5c4c3-c(cc3)ccc3-c3cc4cccnc4cc3)c2cc1 Chemical compound c1cc2cncc(-c3ccc(cc4)c5c3ccc(cc3)c5c4c3-c(cc3)ccc3-c3cc4cccnc4cc3)c2cc1 JVBREHJIOZZCRX-UHFFFAOYSA-N 0.000 description 1
- KGWCLRAGTNMSDJ-UHFFFAOYSA-N c1ccc2ncc(-c(cc3)ccc3-c(cc3)c(ccc(cc4)c56)c5c3ccc6c4-c3cc(cccc4)c4nc3)cc2c1 Chemical compound c1ccc2ncc(-c(cc3)ccc3-c(cc3)c(ccc(cc4)c56)c5c3ccc6c4-c3cc(cccc4)c4nc3)cc2c1 KGWCLRAGTNMSDJ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
-
- 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
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/622—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing four rings, e.g. pyrene
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
- C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
- C07D235/18—Benzimidazoles; Hydrogenated benzimidazoles with aryl radicals directly attached in position 2
-
- 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
- C07D401/10—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 linked by a carbon chain containing aromatic rings
-
- 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
- C07D403/10—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
- 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
-
- 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
-
- 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
- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1011—Condensed systems
-
- 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
- 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
- H10K85/6572—Polycyclic condensed heteroaromatic hydrocarbons comprising only nitrogen in the heteroaromatic polycondensed ring system, e.g. phenanthroline or carbazole
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)
- Quinoline Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Indole Compounds (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2011202764 | 2011-09-16 | ||
JPJP-P-2011-202764 | 2011-09-16 | ||
PCT/JP2012/072420 WO2013038944A1 (ja) | 2011-09-16 | 2012-09-04 | 発光素子材料および発光素子 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20140075674A KR20140075674A (ko) | 2014-06-19 |
KR102040535B1 true KR102040535B1 (ko) | 2019-11-05 |
Family
ID=47883175
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1020147006015A KR102040535B1 (ko) | 2011-09-16 | 2012-09-04 | 발광 소자 재료 및 발광 소자 |
Country Status (5)
Country | Link |
---|---|
JP (1) | JP6020173B2 (zh) |
KR (1) | KR102040535B1 (zh) |
CN (1) | CN103814453B (zh) |
TW (1) | TWI567060B (zh) |
WO (1) | WO2013038944A1 (zh) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2015122459A (ja) * | 2013-12-25 | 2015-07-02 | 三星ディスプレイ株式會社Samsung Display Co.,Ltd. | 有機el素子 |
JP6627507B2 (ja) * | 2014-05-28 | 2020-01-08 | 東レ株式会社 | フルオランテン誘導体、それを含有する電子デバイス、発光素子および光電変換素子 |
TWI569492B (zh) | 2014-12-22 | 2017-02-01 | 昱鐳光電科技股份有限公司 | 有機發光元件 |
JP5988001B1 (ja) * | 2015-01-09 | 2016-09-07 | 東レ株式会社 | 光電変換素子およびこれを用いたイメージセンサ |
JP6646955B2 (ja) * | 2015-06-23 | 2020-02-14 | 三星ディスプレイ株式會社Samsung Display Co.,Ltd. | 有機電界発光素子 |
CN108484507A (zh) * | 2018-04-04 | 2018-09-04 | 长春海谱润斯科技有限公司 | 一种芘类衍生物及其有机发光器件 |
CN108329272A (zh) * | 2018-04-04 | 2018-07-27 | 长春海谱润斯科技有限公司 | 一种含芘结构的有机电致发光材料及其有机发光器件 |
CN109293516B (zh) * | 2018-11-03 | 2022-01-14 | 长春海谱润斯科技股份有限公司 | 一种三芳胺类化合物及其有机发光器件 |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100681027B1 (ko) | 2006-01-16 | 2007-02-09 | 엘지전자 주식회사 | 전계발광소자 및 전자전달 화합물 |
KR100681026B1 (ko) | 2006-01-16 | 2007-02-09 | 엘지전자 주식회사 | 전계발광소자 및 전자전달 화합물 |
KR100681025B1 (ko) | 2006-01-16 | 2007-02-09 | 엘지전자 주식회사 | 전계발광소자 및 전자전달 화합물 |
JP2007066883A (ja) | 2005-08-04 | 2007-03-15 | Canon Inc | 発光素子アレイ及び表示装置 |
JP2009516652A (ja) | 2005-12-13 | 2009-04-23 | エルジー・ケム・リミテッド | 新規のイミダゾキナゾリン誘導体、この製造方法およびこれを用いた有機電気素子 |
JP2009518342A (ja) | 2005-12-08 | 2009-05-07 | メルク パテント ゲーエムベーハー | 有機エレクトロルミネセンス素子のための新規材料 |
JP2012126673A (ja) | 2010-12-15 | 2012-07-05 | Jnc Corp | 縮合ピロール多環化合物、発光層用材料およびこれを用いた有機電界発光素子 |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP3139321B2 (ja) * | 1994-03-31 | 2001-02-26 | 東レ株式会社 | 発光素子 |
JP3424812B2 (ja) * | 1997-12-25 | 2003-07-07 | 日本電気株式会社 | 有機エレクトロルミネッセンス素子 |
EP1582516B1 (en) | 2003-01-10 | 2013-07-17 | Idemitsu Kosan Co., Ltd. | Nitrogenous heterocyclic derivative and organic electroluminescent element employing the same |
DE10356099A1 (de) * | 2003-11-27 | 2005-07-07 | Covion Organic Semiconductors Gmbh | Organisches Elektrolumineszenzelement |
CN101080376A (zh) * | 2004-11-25 | 2007-11-28 | 日本先锋公司 | 芘类化合物和使用了其的发光晶体管元件 |
CN101072743A (zh) * | 2004-11-25 | 2007-11-14 | 日本先锋公司 | 芘类化合物和使用了其的发光晶体管元件以及有机电致发光元件 |
JP2006176491A (ja) * | 2004-11-25 | 2006-07-06 | Kyoto Univ | ピレン系化合物及びこれを用いた発光トランジスタ素子 |
JP2007015961A (ja) | 2005-07-06 | 2007-01-25 | Idemitsu Kosan Co Ltd | ピレン誘導体及びそれらを用いた有機エレクトロルミネッセンス素子 |
CN101258221B (zh) * | 2005-09-08 | 2013-04-03 | 东丽株式会社 | 发光元件材料和发光元件 |
JP2007131723A (ja) | 2005-11-10 | 2007-05-31 | Toray Ind Inc | 発光素子材料および発光素子 |
JP2007169581A (ja) * | 2005-11-25 | 2007-07-05 | Toray Ind Inc | 発光素子材料および発光素子 |
US7811681B2 (en) | 2006-01-16 | 2010-10-12 | Lg Display Co., Ltd. | Electron transport compound and organic light emitting device comprising the same |
KR101026171B1 (ko) * | 2008-07-01 | 2011-04-05 | 덕산하이메탈(주) | 신규의 축합 카바졸 유도체 및 이를 포함하는 유기전계발광 소자 |
KR101247626B1 (ko) * | 2008-09-04 | 2013-03-29 | 제일모직주식회사 | 유기광전소자용 화합물 및 이를 포함하는 유기광전소자 |
JP2010195708A (ja) * | 2009-02-25 | 2010-09-09 | Toyo Ink Mfg Co Ltd | カルバゾリル基を有する化合物およびその用途 |
DE102009023155A1 (de) * | 2009-05-29 | 2010-12-02 | Merck Patent Gmbh | Materialien für organische Elektrolumineszenzvorrichtungen |
JP5640460B2 (ja) | 2009-06-03 | 2014-12-17 | 東レ株式会社 | 発光素子および発光素子材料 |
JP5423171B2 (ja) * | 2009-06-19 | 2014-02-19 | 東洋インキScホールディングス株式会社 | 有機エレクトロルミネッセンス素子用材料およびその用途 |
KR101408515B1 (ko) * | 2009-07-01 | 2014-06-17 | 주식회사 엘지화학 | 신규한 화합물 및 이를 이용한 유기 전자 소자 |
CN101597259B (zh) * | 2009-07-07 | 2012-11-07 | 清华大学 | 有机材料及其在有机电致发光器件中的应用 |
KR101245243B1 (ko) * | 2009-12-16 | 2013-03-19 | 덕산하이메탈(주) | 스피로 카바졸 화합물 및 이를 이용한 유기전기소자, 그 단말 |
JP2011173972A (ja) * | 2010-02-24 | 2011-09-08 | Toyo Ink Sc Holdings Co Ltd | 有機エレクトロルミネッセンス素子用材料およびその用途 |
-
2012
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Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007066883A (ja) | 2005-08-04 | 2007-03-15 | Canon Inc | 発光素子アレイ及び表示装置 |
JP2009518342A (ja) | 2005-12-08 | 2009-05-07 | メルク パテント ゲーエムベーハー | 有機エレクトロルミネセンス素子のための新規材料 |
JP2009516652A (ja) | 2005-12-13 | 2009-04-23 | エルジー・ケム・リミテッド | 新規のイミダゾキナゾリン誘導体、この製造方法およびこれを用いた有機電気素子 |
KR100681027B1 (ko) | 2006-01-16 | 2007-02-09 | 엘지전자 주식회사 | 전계발광소자 및 전자전달 화합물 |
KR100681026B1 (ko) | 2006-01-16 | 2007-02-09 | 엘지전자 주식회사 | 전계발광소자 및 전자전달 화합물 |
KR100681025B1 (ko) | 2006-01-16 | 2007-02-09 | 엘지전자 주식회사 | 전계발광소자 및 전자전달 화합물 |
JP2012126673A (ja) | 2010-12-15 | 2012-07-05 | Jnc Corp | 縮合ピロール多環化合物、発光層用材料およびこれを用いた有機電界発光素子 |
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WO2013038944A1 (ja) | 2013-03-21 |
CN103814453A (zh) | 2014-05-21 |
JPWO2013038944A1 (ja) | 2015-03-26 |
JP6020173B2 (ja) | 2016-11-02 |
KR20140075674A (ko) | 2014-06-19 |
TWI567060B (zh) | 2017-01-21 |
CN103814453B (zh) | 2016-12-28 |
TW201319044A (zh) | 2013-05-16 |
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