KR20100092451A - 디페닐아미노-비스(페녹시)- 및 비스(디페닐아미노)-페녹시트리아진 화합물의 용도 - Google Patents
디페닐아미노-비스(페녹시)- 및 비스(디페닐아미노)-페녹시트리아진 화합물의 용도 Download PDFInfo
- Publication number
- KR20100092451A KR20100092451A KR1020107011307A KR20107011307A KR20100092451A KR 20100092451 A KR20100092451 A KR 20100092451A KR 1020107011307 A KR1020107011307 A KR 1020107011307A KR 20107011307 A KR20107011307 A KR 20107011307A KR 20100092451 A KR20100092451 A KR 20100092451A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- radicals
- aryl
- formula
- compound
- 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.)
- Withdrawn
Links
- MGNCLNQXLYJVJD-UHFFFAOYSA-N Clc1nc(Cl)nc(Cl)n1 Chemical compound Clc1nc(Cl)nc(Cl)n1 MGNCLNQXLYJVJD-UHFFFAOYSA-N 0.000 description 4
- WCVKYWWCDYHMNJ-UHFFFAOYSA-N Cc(cc1)ccc1N(c1ccc(C)cc1)c1nc(N(c2ccc(C)cc2)c2ccc(C)cc2)nc(Cl)n1 Chemical compound Cc(cc1)ccc1N(c1ccc(C)cc1)c1nc(N(c2ccc(C)cc2)c2ccc(C)cc2)nc(Cl)n1 WCVKYWWCDYHMNJ-UHFFFAOYSA-N 0.000 description 2
- JNNIAVRLVSYKCB-UHFFFAOYSA-N Cc1cccc(N(c2ccccc2)c2nc(Cl)nc(N(c3ccccc3)c3cc(C)ccc3)n2)c1 Chemical compound Cc1cccc(N(c2ccccc2)c2nc(Cl)nc(N(c3ccccc3)c3cc(C)ccc3)n2)c1 JNNIAVRLVSYKCB-UHFFFAOYSA-N 0.000 description 2
- 0 Cc(cc1)c(C)cc1Oc1nc(*)nc(N(c2c(*)c(C)c(C)c(*)c2*)c2c(*)c(*)c(*)c(*)c2*)n1 Chemical compound Cc(cc1)c(C)cc1Oc1nc(*)nc(N(c2c(*)c(C)c(C)c(*)c2*)c2c(*)c(*)c(*)c(*)c2*)n1 0.000 description 1
- RYHAZLAEKPWLJK-UHFFFAOYSA-N Cc(cc1)ccc1N(c1ccc(C)cc1)c1nc(N(c2ccc(C)cc2)c2ccc(C)cc2)nc(Oc2cc(C)cc(C)c2)n1 Chemical compound Cc(cc1)ccc1N(c1ccc(C)cc1)c1nc(N(c2ccc(C)cc2)c2ccc(C)cc2)nc(Oc2cc(C)cc(C)c2)n1 RYHAZLAEKPWLJK-UHFFFAOYSA-N 0.000 description 1
- UVFUDVMDHQVBAQ-UHFFFAOYSA-N Cc(cc1c2c3ccc(C)c2)ccc1[n]3-c(cc1)ccc1O Chemical compound Cc(cc1c2c3ccc(C)c2)ccc1[n]3-c(cc1)ccc1O UVFUDVMDHQVBAQ-UHFFFAOYSA-N 0.000 description 1
- CZMMNWBZGDOULJ-UHFFFAOYSA-N Cc(cc1c2c3ccc(C)c2)ccc1[n]3-c(cc1)ccc1OC Chemical compound Cc(cc1c2c3ccc(C)c2)ccc1[n]3-c(cc1)ccc1OC CZMMNWBZGDOULJ-UHFFFAOYSA-N 0.000 description 1
- PSABTELWGCYCMX-UHFFFAOYSA-N Cc1cccc(N(c2ccccc2)c2nc(Oc3cc(C)cc(C)c3)nc(N(c3ccccc3)c3cc(C)ccc3)n2)c1 Chemical compound Cc1cccc(N(c2ccccc2)c2nc(Oc3cc(C)cc(C)c3)nc(N(c3ccccc3)c3cc(C)ccc3)n2)c1 PSABTELWGCYCMX-UHFFFAOYSA-N 0.000 description 1
- WPAYYYDSSCOEHN-UHFFFAOYSA-N Clc1nc(Oc2ccccc2)nc(Oc2ccccc2)n1 Chemical compound Clc1nc(Oc2ccccc2)nc(Oc2ccccc2)n1 WPAYYYDSSCOEHN-UHFFFAOYSA-N 0.000 description 1
- YGXMMMPUTDCEAF-UHFFFAOYSA-N c(cc1)ccc1N(c1ccccc1)c1nc(N(c2ccccc2)c2ccccc2)nc(N(c2ccccc2)c2ccccc2)n1 Chemical compound c(cc1)ccc1N(c1ccccc1)c1nc(N(c2ccccc2)c2ccccc2)nc(N(c2ccccc2)c2ccccc2)n1 YGXMMMPUTDCEAF-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- 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
- H05B33/20—Light sources with substantially two-dimensional radiating surfaces characterised by the chemical or physical composition or the arrangement of the material in which the electroluminescent material is embedded
-
- 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]
- H10K50/18—Carrier blocking 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
- H10K85/30—Coordination compounds
- H10K85/321—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3]
- H10K85/324—Metal complexes comprising a group IIIA element, e.g. Tris (8-hydroxyquinoline) gallium [Gaq3] comprising aluminium, e.g. Alq3
-
- 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
-
- 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
- H10K85/633—Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine comprising polycyclic condensed aromatic hydrocarbons as substituents on the 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
- H10K85/631—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
-
- 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
- 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
- H10K2102/00—Constructional details relating to the organic devices covered by this subclass
Landscapes
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Optics & Photonics (AREA)
- Inorganic Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Electroluminescent Light Sources (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07119142 | 2007-10-24 | ||
| EP07119142.3 | 2007-10-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20100092451A true KR20100092451A (ko) | 2010-08-20 |
Family
ID=40120132
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020107011307A Withdrawn KR20100092451A (ko) | 2007-10-24 | 2008-10-21 | 디페닐아미노-비스(페녹시)- 및 비스(디페닐아미노)-페녹시트리아진 화합물의 용도 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US20100258790A1 (enExample) |
| EP (1) | EP2206175A1 (enExample) |
| JP (1) | JP2011502189A (enExample) |
| KR (1) | KR20100092451A (enExample) |
| CN (1) | CN101884122B (enExample) |
| WO (1) | WO2009053346A1 (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2009053278A1 (de) * | 2007-10-24 | 2009-04-30 | Basf Se | Verwendung von substituierten tris(diphenylamino)-triazinverbindungen in oleds |
| KR102125199B1 (ko) | 2012-07-23 | 2020-06-22 | 메르크 파텐트 게엠베하 | 유기 전계발광 소자용 재료 |
| WO2014106524A2 (de) * | 2013-01-03 | 2014-07-10 | Merck Patent Gmbh | Materialien für elektronische vorrichtungen |
| KR102129508B1 (ko) * | 2017-07-14 | 2020-07-02 | 삼성에스디아이 주식회사 | 유기 광전자 소자용 조성물, 유기 광전자 소자 및 표시 장치 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3966680A (en) * | 1973-12-13 | 1976-06-29 | Minnesota Mining And Manufacturing Company | Phenoxy-s-triazine chain coupler for polyesterification and novel polyesters |
| JP3691101B2 (ja) * | 1995-01-24 | 2005-08-31 | 三洋電機株式会社 | 有機エレクトロルミネッセンス素子 |
| US6821645B2 (en) * | 1999-12-27 | 2004-11-23 | Fuji Photo Film Co., Ltd. | Light-emitting material comprising orthometalated iridium complex, light-emitting device, high efficiency red light-emitting device, and novel iridium complex |
| US6565994B2 (en) * | 2000-02-10 | 2003-05-20 | Fuji Photo Film Co., Ltd. | Light emitting device material comprising iridium complex and light emitting device using same material |
| US7306856B2 (en) * | 2000-07-17 | 2007-12-11 | Fujifilm Corporation | Light-emitting element and iridium complex |
| JP4344494B2 (ja) * | 2000-08-24 | 2009-10-14 | 富士フイルム株式会社 | 発光素子及び新規重合体子 |
| JP4067286B2 (ja) * | 2000-09-21 | 2008-03-26 | 富士フイルム株式会社 | 発光素子及びイリジウム錯体 |
| JP4086499B2 (ja) * | 2000-11-29 | 2008-05-14 | キヤノン株式会社 | 金属配位化合物、発光素子及び表示装置 |
| EP2256838B1 (en) * | 2001-08-29 | 2018-12-12 | The Trustees of Princeton University | Organic light emitting devices having charge carrier blocking layers comprising metalcomplexes |
| JP4365199B2 (ja) * | 2002-12-27 | 2009-11-18 | 富士フイルム株式会社 | 有機電界発光素子 |
| DE10338550A1 (de) * | 2003-08-19 | 2005-03-31 | Basf Ag | Übergangsmetallkomplexe mit Carbenliganden als Emitter für organische Licht-emittierende Dioden (OLEDs) |
| JP4541809B2 (ja) * | 2004-09-08 | 2010-09-08 | キヤノン株式会社 | 有機化合物及び有機発光素子 |
| US20060073360A1 (en) * | 2004-09-28 | 2006-04-06 | Fuji Photo Film Co., Ltd. | Organic electroluminescent device |
| JP4655590B2 (ja) * | 2004-11-08 | 2011-03-23 | Jsr株式会社 | 発光剤およびその製造方法、発光性組成物並びに有機エレクトロルミネッセンス素子 |
| CN1749254A (zh) * | 2005-09-01 | 2006-03-22 | 复旦大学 | 含杂原子双螺环材料及其合成方法和应用 |
| WO2009053278A1 (de) * | 2007-10-24 | 2009-04-30 | Basf Se | Verwendung von substituierten tris(diphenylamino)-triazinverbindungen in oleds |
-
2008
- 2008-10-21 CN CN2008801186424A patent/CN101884122B/zh not_active Expired - Fee Related
- 2008-10-21 KR KR1020107011307A patent/KR20100092451A/ko not_active Withdrawn
- 2008-10-21 US US12/738,231 patent/US20100258790A1/en not_active Abandoned
- 2008-10-21 WO PCT/EP2008/064178 patent/WO2009053346A1/de not_active Ceased
- 2008-10-21 JP JP2010530423A patent/JP2011502189A/ja not_active Withdrawn
- 2008-10-21 EP EP08842691A patent/EP2206175A1/de not_active Withdrawn
Also Published As
| Publication number | Publication date |
|---|---|
| CN101884122B (zh) | 2012-06-06 |
| WO2009053346A1 (de) | 2009-04-30 |
| JP2011502189A (ja) | 2011-01-20 |
| EP2206175A1 (de) | 2010-07-14 |
| CN101884122A (zh) | 2010-11-10 |
| US20100258790A1 (en) | 2010-10-14 |
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St.27 status event code: A-2-2-P10-P11-nap-X000 |
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| P13-X000 | Application amended |
St.27 status event code: A-2-2-P10-P13-nap-X000 |
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St.27 status event code: A-1-1-Q10-Q12-nap-PG1501 |
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| PC1203 | Withdrawal of no request for examination |
St.27 status event code: N-1-6-B10-B12-nap-PC1203 |
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| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid | ||
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St.27 status event code: A-3-3-R10-R18-oth-X000 |
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St.27 status event code: A-3-3-R10-R18-oth-X000 |
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| P22-X000 | Classification modified |
St.27 status event code: A-2-2-P10-P22-nap-X000 |
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