CN101838262B - 具有杂芳环的咔唑衍生物及使用它的发光元件及发光装置 - Google Patents
具有杂芳环的咔唑衍生物及使用它的发光元件及发光装置 Download PDFInfo
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- CN101838262B CN101838262B CN201010145971.7A CN201010145971A CN101838262B CN 101838262 B CN101838262 B CN 101838262B CN 201010145971 A CN201010145971 A CN 201010145971A CN 101838262 B CN101838262 B CN 101838262B
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- Prior art keywords
- carbazole derivative
- luminous element
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- carbon
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- 0 Cc1nc(cccc2)c2nc1*[Al] Chemical compound Cc1nc(cccc2)c2nc1*[Al] 0.000 description 6
- RZROBPBNWNHSSG-UHFFFAOYSA-N N=C(c1ccccc1)OC(c(cc1)ccc1-[n]1c(ccc(-c(cc2)cc(c3ccccc33)c2[n]3-c2ccccc2)c2)c2c2c1cccc2)=N Chemical compound N=C(c1ccccc1)OC(c(cc1)ccc1-[n]1c(ccc(-c(cc2)cc(c3ccccc33)c2[n]3-c2ccccc2)c2)c2c2c1cccc2)=N RZROBPBNWNHSSG-UHFFFAOYSA-N 0.000 description 2
- QLZNFHGSXRIHFV-UHFFFAOYSA-N C(C(C=CC=C1)C=C2)C=C1C=C2C1=[N]=C(c(cc2)ccc2Nc(cc2)ccc2-c(cc2)cc(c3ccccc33)c2[n]3-c2ccccc2)O1 Chemical compound C(C(C=CC=C1)C=C2)C=C1C=C2C1=[N]=C(c(cc2)ccc2Nc(cc2)ccc2-c(cc2)cc(c3ccccc33)c2[n]3-c2ccccc2)O1 QLZNFHGSXRIHFV-UHFFFAOYSA-N 0.000 description 1
- SUMBMVMLYYTYIX-XMKRSPLQSA-N C/C=C\C(\C1=[N]=C(c2ccccc2)O1)=C/C=C/[n](c(cccc1)c1c1c2)c1ccc2-c(cc1)cc(c2c3cccc2)c1[n]3-c(cc1)ccc1-c1ccccc1 Chemical compound C/C=C\C(\C1=[N]=C(c2ccccc2)O1)=C/C=C/[n](c(cccc1)c1c1c2)c1ccc2-c(cc1)cc(c2c3cccc2)c1[n]3-c(cc1)ccc1-c1ccccc1 SUMBMVMLYYTYIX-XMKRSPLQSA-N 0.000 description 1
- HBXXJZDXOAWJTN-UHFFFAOYSA-N CC(C)(C)c(cc1c2cc(-c(cc3c4c5cccc4)ccc3[n]5-c3ccccc3)ccc22)ccc1[n]2-c(cc1)ccc1-c1nc2ccccc2nc1-c1ccccc1 Chemical compound CC(C)(C)c(cc1c2cc(-c(cc3c4c5cccc4)ccc3[n]5-c3ccccc3)ccc22)ccc1[n]2-c(cc1)ccc1-c1nc2ccccc2nc1-c1ccccc1 HBXXJZDXOAWJTN-UHFFFAOYSA-N 0.000 description 1
- PHDPGGPCFIMNRD-UHFFFAOYSA-N CC(C1c2c3ccc(-c(cc4c5c6cccc5)ccc4[n]6-c4ccccc4)c2)C(c2cccc4c2cccc4)=CC=C1N3c(cc1)ccc1C1=Nc(cccc2)c2NC1c1ccccc1 Chemical compound CC(C1c2c3ccc(-c(cc4c5c6cccc5)ccc4[n]6-c4ccccc4)c2)C(c2cccc4c2cccc4)=CC=C1N3c(cc1)ccc1C1=Nc(cccc2)c2NC1c1ccccc1 PHDPGGPCFIMNRD-UHFFFAOYSA-N 0.000 description 1
- PZUIKZUJJQYWQF-UHFFFAOYSA-N CC1(C=CC(c2nc3ccccc3nc2-c2ccccc2)=CC1)[n](c(c(c1c2)c3)ccc3-c3ccccc3)c1ccc2-c(cc1)cc(c2c3cccc2)c1[n]3-c1ccccc1 Chemical compound CC1(C=CC(c2nc3ccccc3nc2-c2ccccc2)=CC1)[n](c(c(c1c2)c3)ccc3-c3ccccc3)c1ccc2-c(cc1)cc(c2c3cccc2)c1[n]3-c1ccccc1 PZUIKZUJJQYWQF-UHFFFAOYSA-N 0.000 description 1
- BZTFDQARRUKVJL-UHFFFAOYSA-N CC1(C=CCCC11)c2cc(-c(cc3c4ccccc44)ccc3[n]4-c3ccccc3)ccc2N1c(cc1)ccc1C(OC(c1ccccc1)=N)=N Chemical compound CC1(C=CCCC11)c2cc(-c(cc3c4ccccc44)ccc3[n]4-c3ccccc3)ccc2N1c(cc1)ccc1C(OC(c1ccccc1)=N)=N BZTFDQARRUKVJL-UHFFFAOYSA-N 0.000 description 1
- MSBLUYJBRFJUPS-UHFFFAOYSA-N CCc(cc1c2c3ccc(-c(cc4C5(C)C=CC=CC55)ccc4N5c4ccccc4)c2)ccc1[n]3-c(cc1)ccc1C1=Nc(cccc2)c2NC1c1ccccc1 Chemical compound CCc(cc1c2c3ccc(-c(cc4C5(C)C=CC=CC55)ccc4N5c4ccccc4)c2)ccc1[n]3-c(cc1)ccc1C1=Nc(cccc2)c2NC1c1ccccc1 MSBLUYJBRFJUPS-UHFFFAOYSA-N 0.000 description 1
- BQFLTJFFUFYLCN-UHFFFAOYSA-O Cc(cc1)ccc1-[n]1c(ccc(C(C=C2c3c4cccc3)=CCC2N4c(cc2)ccc2C(OC(c2ccccc2)=[NH2+])=N)c2)c2c2ccccc12 Chemical compound Cc(cc1)ccc1-[n]1c(ccc(C(C=C2c3c4cccc3)=CCC2N4c(cc2)ccc2C(OC(c2ccccc2)=[NH2+])=N)c2)c2c2ccccc12 BQFLTJFFUFYLCN-UHFFFAOYSA-O 0.000 description 1
- CKRDWHMQICESSB-UHFFFAOYSA-N Cc(cc1c2cc(-c(cc3)cc(c4c5cccc4)c3[n]5-c3ccccc3)ccc22)ccc1[n]2-c(cc1)ccc1C(OC(c1ccccc1)=N)=N Chemical compound Cc(cc1c2cc(-c(cc3)cc(c4c5cccc4)c3[n]5-c3ccccc3)ccc22)ccc1[n]2-c(cc1)ccc1C(OC(c1ccccc1)=N)=N CKRDWHMQICESSB-UHFFFAOYSA-N 0.000 description 1
- DFLHXPSRQROJQD-UHFFFAOYSA-O N=C(c(cc1)ccc1-[n]1c(ccc(-c(cc2c3c4cccc3)ccc2[n]4-c2c(cccc3)c3ccc2)c2)c2c2ccccc12)OC(c1ccccc1)=[NH2+] Chemical compound N=C(c(cc1)ccc1-[n]1c(ccc(-c(cc2c3c4cccc3)ccc2[n]4-c2c(cccc3)c3ccc2)c2)c2c2ccccc12)OC(c1ccccc1)=[NH2+] DFLHXPSRQROJQD-UHFFFAOYSA-O 0.000 description 1
- PYKMDYMUCHPTIK-UHFFFAOYSA-O N=C(c(cc1)ccc1Br)OC(c1ccccc1)=[NH2+] Chemical compound N=C(c(cc1)ccc1Br)OC(c1ccccc1)=[NH2+] PYKMDYMUCHPTIK-UHFFFAOYSA-O 0.000 description 1
- XCYLKVXNTKFRGE-UHFFFAOYSA-N N=C(c1ccccc1)OC(c(cc1)ccc1-[n](c(cccc1)c1c1c2)c1ccc2-c(cc1)cc(c2cc(-c3cc4ccccc4cc3)ccc22)c1[n]2-c1ccccc1)=N Chemical compound N=C(c1ccccc1)OC(c(cc1)ccc1-[n](c(cccc1)c1c1c2)c1ccc2-c(cc1)cc(c2cc(-c3cc4ccccc4cc3)ccc22)c1[n]2-c1ccccc1)=N XCYLKVXNTKFRGE-UHFFFAOYSA-N 0.000 description 1
- LKSKXEMMSBCGSV-UHFFFAOYSA-N N=C(c1ccccc1)OC(c(cc1)ccc1-[n](c1ccccc1c1c2)c1ccc2-c(cc1)cc(c2c3cccc2)c1[n]3-c(cc1)ccc1-c1cccc2c1cccc2)=N Chemical compound N=C(c1ccccc1)OC(c(cc1)ccc1-[n](c1ccccc1c1c2)c1ccc2-c(cc1)cc(c2c3cccc2)c1[n]3-c(cc1)ccc1-c1cccc2c1cccc2)=N LKSKXEMMSBCGSV-UHFFFAOYSA-N 0.000 description 1
- USPIQLUWOLTQNR-UHFFFAOYSA-N N=C(c1ccccc1)OC(c(cc1)ccc1N(c1ccccc1)c(cc1)ccc1-c(cc1)cc(c2ccccc22)c1[n]2-c1cc(cccc2)c2cc1)=N Chemical compound N=C(c1ccccc1)OC(c(cc1)ccc1N(c1ccccc1)c(cc1)ccc1-c(cc1)cc(c2ccccc22)c1[n]2-c1cc(cccc2)c2cc1)=N USPIQLUWOLTQNR-UHFFFAOYSA-N 0.000 description 1
- KAXMNTNYAYUHRS-UHFFFAOYSA-N N=C(c1ccccc1)OC(c(cc1)ccc1N(c1ccccc1)c(cc1)ccc1-c(cc1c2c3ccc(-c4c(cccc5)c5ccc4)c2)ccc1[n]3-c1ccccc1)=N Chemical compound N=C(c1ccccc1)OC(c(cc1)ccc1N(c1ccccc1)c(cc1)ccc1-c(cc1c2c3ccc(-c4c(cccc5)c5ccc4)c2)ccc1[n]3-c1ccccc1)=N KAXMNTNYAYUHRS-UHFFFAOYSA-N 0.000 description 1
- PCDIUTBXUUFGLG-UHFFFAOYSA-N N=C(c1ccccc1)OC(c(cc1)ccc1N(c1ccccc1)c(cc1)ccc1-c(cc1c2c3ccc(-c4ccccc4)c2)ccc1[n]3-c1ccccc1)=N Chemical compound N=C(c1ccccc1)OC(c(cc1)ccc1N(c1ccccc1)c(cc1)ccc1-c(cc1c2c3ccc(-c4ccccc4)c2)ccc1[n]3-c1ccccc1)=N PCDIUTBXUUFGLG-UHFFFAOYSA-N 0.000 description 1
- GKTLHQFSIDFAJH-UHFFFAOYSA-N c(cc1)ccc1-[n](c(cccc1)c1c1c2)c1ccc2-c1ccc2[nH]c3ccccc3c2c1 Chemical compound c(cc1)ccc1-[n](c(cccc1)c1c1c2)c1ccc2-c1ccc2[nH]c3ccccc3c2c1 GKTLHQFSIDFAJH-UHFFFAOYSA-N 0.000 description 1
- AKZPWKSTKKXRDF-UHFFFAOYSA-N c(cc1)ccc1-c1ccc(c(cc(cc2)-c(cc3c4ccccc44)ccc3[n]4-c3ccccc3)c2[n]2-c(cc3)ccc3-c3nc4ccccc4nc3-c3ccccc3)c2c1 Chemical compound c(cc1)ccc1-c1ccc(c(cc(cc2)-c(cc3c4ccccc44)ccc3[n]4-c3ccccc3)c2[n]2-c(cc3)ccc3-c3nc4ccccc4nc3-c3ccccc3)c2c1 AKZPWKSTKKXRDF-UHFFFAOYSA-N 0.000 description 1
- PEJUOWCFILWAEL-UHFFFAOYSA-N c(cc1)ccc1-c1nc2ccccc2nc1-c(cc1)ccc1-[n]1c(ccc(-c(cc2c3ccccc33)ccc2[n]3-c2ccccc2)c2)c2c2c1cccc2 Chemical compound c(cc1)ccc1-c1nc2ccccc2nc1-c(cc1)ccc1-[n]1c(ccc(-c(cc2c3ccccc33)ccc2[n]3-c2ccccc2)c2)c2c2c1cccc2 PEJUOWCFILWAEL-UHFFFAOYSA-N 0.000 description 1
- CURFGOZVXAKDBY-UHFFFAOYSA-N c1ccc(C2Nc(cccc3)c3N=C2c(cc2)ccc2-[n](c(c(c2c3)c4)ccc4-c(cc4c5c6cccc5)ccc4[n]6-c4ccccc4)c2ccc3-c2cc3ccccc3cc2)cc1 Chemical compound c1ccc(C2Nc(cccc3)c3N=C2c(cc2)ccc2-[n](c(c(c2c3)c4)ccc4-c(cc4c5c6cccc5)ccc4[n]6-c4ccccc4)c2ccc3-c2cc3ccccc3cc2)cc1 CURFGOZVXAKDBY-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
-
- 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
- C07D403/12—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 chain containing hetero atoms as chain links
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- 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
- C07D403/14—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 three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
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- 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 [2D] radiating surfaces
- H05B33/20—Light sources with substantially two-dimensional [2D] radiating surfaces characterised by the chemical or physical composition or the arrangement of the material in which the electroluminescent material is embedded
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- 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
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K59/00—Integrated devices, or assemblies of multiple devices, comprising at least one organic light-emitting element covered by group H10K50/00
- H10K59/10—OLED displays
- H10K59/17—Passive-matrix OLED displays
- H10K59/173—Passive-matrix OLED displays comprising banks or shadow masks
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- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10K—ORGANIC ELECTRIC SOLID-STATE DEVICES
- H10K59/00—Integrated devices, or assemblies of multiple devices, comprising at least one organic light-emitting element covered by group H10K50/00
- H10K59/30—Devices specially adapted for multicolour light emission
- H10K59/32—Stacked devices having two or more layers, each emitting at different wavelengths
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- 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
- H10K85/30—Coordination compounds
- H10K85/341—Transition metal complexes, e.g. Ru(II)polypyridine complexes
- H10K85/342—Transition metal complexes, e.g. Ru(II)polypyridine complexes comprising iridium
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- 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
- H10K85/631—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
- H10K85/636—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising heteroaromatic hydrocarbons as substituents on the nitrogen atom
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- 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
- H10K85/656—Aromatic compounds comprising a hetero atom comprising two or more different heteroatoms per ring
- H10K85/6565—Oxadiazole compounds
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- 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
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02B—CLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO BUILDINGS, e.g. HOUSING, HOUSE APPLIANCES OR RELATED END-USER APPLICATIONS
- Y02B20/00—Energy efficient lighting technologies, e.g. halogen lamps or gas discharge lamps
- Y02B20/30—Semiconductor lamps, e.g. solid state lamps [SSL] light emitting diodes [LED] or organic LED [OLED]
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- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Crystallography & Structural Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Optics & Photonics (AREA)
- Electroluminescent Light Sources (AREA)
- Plural Heterocyclic Compounds (AREA)
- Devices For Indicating Variable Information By Combining Individual Elements (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2009069177 | 2009-03-20 | ||
| JP2009-069177 | 2009-03-20 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101838262A CN101838262A (zh) | 2010-09-22 |
| CN101838262B true CN101838262B (zh) | 2014-07-23 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201010145971.7A Expired - Fee Related CN101838262B (zh) | 2009-03-20 | 2010-03-19 | 具有杂芳环的咔唑衍生物及使用它的发光元件及发光装置 |
Country Status (5)
| Country | Link |
|---|---|
| US (3) | US20100237773A1 (enExample) |
| JP (6) | JP5607959B2 (enExample) |
| KR (1) | KR101547876B1 (enExample) |
| CN (1) | CN101838262B (enExample) |
| TW (2) | TWI525089B (enExample) |
Families Citing this family (47)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5709389B2 (ja) * | 2009-03-20 | 2015-04-30 | 株式会社半導体エネルギー研究所 | オキサジアゾール誘導体、発光素子、発光装置及び電子機器 |
| TWI525089B (zh) * | 2009-03-20 | 2016-03-11 | 半導體能源研究所股份有限公司 | 具有雜芳香族環之咔唑衍生物及使用具有雜芳香族環之咔唑衍生物的發光元件、發光裝置和電子裝置 |
| JP2010254671A (ja) * | 2009-03-31 | 2010-11-11 | Semiconductor Energy Lab Co Ltd | カルバゾール誘導体、発光素子用材料、発光素子、発光装置、電子機器、及び照明装置 |
| TW201120064A (en) * | 2009-06-24 | 2011-06-16 | Georgia Tech Res Inst | Polymeric ambipolar hosts for phosphorescent guest emitters |
| KR101431644B1 (ko) * | 2009-08-10 | 2014-08-21 | 롬엔드하스전자재료코리아유한회사 | 신규한 유기 발광 화합물 및 이를 포함하는 유기 전계 발광 소자 |
| US8637857B2 (en) * | 2010-04-06 | 2014-01-28 | Basf Se | Substituted carbazole derivatives and use thereof in organic electronics |
| JP5562970B2 (ja) * | 2010-04-20 | 2014-07-30 | 出光興産株式会社 | ビスカルバゾール誘導体、有機エレクトロルミネッセンス素子用材料及びそれを用いた有機エレクトロルミネッセンス素子 |
| KR20110122051A (ko) | 2010-05-03 | 2011-11-09 | 제일모직주식회사 | 유기광전소자용 화합물 및 이를 포함하는 유기광전소자 |
| CN102884156B (zh) * | 2010-06-24 | 2016-01-20 | 东丽株式会社 | 发光元件材料和发光元件 |
| EP2599851A4 (en) * | 2010-07-30 | 2013-12-11 | Rohm & Haas Elect Mat | ORGANIC ELECTROLUMINESCENCE DEVICE WITH AN ORGANIC LIGHT-EMITTING DEVICE AS A LIGHT-EMITTING MATERIAL |
| US9954180B2 (en) | 2010-08-20 | 2018-04-24 | Universal Display Corporation | Bicarbazole compounds for OLEDs |
| JP2012156499A (ja) * | 2011-01-05 | 2012-08-16 | Idemitsu Kosan Co Ltd | 有機エレクトロルミネッセンス素子 |
| EP2674418B1 (en) * | 2011-02-07 | 2021-01-06 | Idemitsu Kosan Co., Ltd. | Biscarbazole derivative and organic electroluminescent element using same |
| KR101874657B1 (ko) | 2011-02-07 | 2018-07-04 | 이데미쓰 고산 가부시키가이샤 | 비스카바졸 유도체 및 그것을 이용한 유기 전기발광 소자 |
| KR20140043043A (ko) * | 2011-02-11 | 2014-04-08 | 유니버셜 디스플레이 코포레이션 | 유기 발광 디바이스 및 이것에 사용되는 재료 |
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| JP2015024997A (ja) | 2015-02-05 |
| KR20100105501A (ko) | 2010-09-29 |
| KR101547876B1 (ko) | 2015-08-27 |
| JP2010241801A (ja) | 2010-10-28 |
| US8247575B2 (en) | 2012-08-21 |
| JP2019220693A (ja) | 2019-12-26 |
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