WO2012148127A2 - Composé, élément électronique organique l'utilisant et dispositif électronique associé - Google Patents
Composé, élément électronique organique l'utilisant et dispositif électronique associé Download PDFInfo
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- WO2012148127A2 WO2012148127A2 PCT/KR2012/002990 KR2012002990W WO2012148127A2 WO 2012148127 A2 WO2012148127 A2 WO 2012148127A2 KR 2012002990 W KR2012002990 W KR 2012002990W WO 2012148127 A2 WO2012148127 A2 WO 2012148127A2
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- 0 *(c1c(cccc2)c2ccc1)c1cccc2c1cccc2-c(cc1)cc2c1c(ccc(-c1cc3ccccc3cc1)c1)c1[o]2 Chemical compound *(c1c(cccc2)c2ccc1)c1cccc2c1cccc2-c(cc1)cc2c1c(ccc(-c1cc3ccccc3cc1)c1)c1[o]2 0.000 description 7
- DXGCDBBGCIXZGL-UHFFFAOYSA-N C1C=C(c(cc2)cc(c3cc(-c4ccc(cccc5)c5c4)ccc33)c2[n]3-c2cccc3c2cccc3)c2cccc(Sc3cccc4ccccc34)c2C1 Chemical compound C1C=C(c(cc2)cc(c3cc(-c4ccc(cccc5)c5c4)ccc33)c2[n]3-c2cccc3c2cccc3)c2cccc(Sc3cccc4ccccc34)c2C1 DXGCDBBGCIXZGL-UHFFFAOYSA-N 0.000 description 1
- ZVDBJLHKEXUKOZ-UHFFFAOYSA-N Oc(c(-c(cc1)c(cccc2)c2c1Oc(c1c2cccc1)c(cccc1)c1c2-c1c(cccc2)c2c(-c2cc(cccc3)c3cc2)c2c1cccc2)c(c(O)c1O)O)c1O Chemical compound Oc(c(-c(cc1)c(cccc2)c2c1Oc(c1c2cccc1)c(cccc1)c1c2-c1c(cccc2)c2c(-c2cc(cccc3)c3cc2)c2c1cccc2)c(c(O)c1O)O)c1O ZVDBJLHKEXUKOZ-UHFFFAOYSA-N 0.000 description 1
- FIDXRAGOCYPFJZ-UHFFFAOYSA-N c(cc1)cc(cc2)c1cc2-c(c1c2cccc1)c(cccc1)c1c2-c1cccc2c1cc(cccc1)c1c2Oc1c(cccc2)c2ccc1 Chemical compound c(cc1)cc(cc2)c1cc2-c(c1c2cccc1)c(cccc1)c1c2-c1cccc2c1cc(cccc1)c1c2Oc1c(cccc2)c2ccc1 FIDXRAGOCYPFJZ-UHFFFAOYSA-N 0.000 description 1
- PAOWERWJVKTKID-UHFFFAOYSA-N c(cc1)cc(cc2)c1cc2-c(cc1)ccc1-c(cc1)c(cccc2)c2c1Oc1c(cccc2)c2ccc1 Chemical compound c(cc1)cc(cc2)c1cc2-c(cc1)ccc1-c(cc1)c(cccc2)c2c1Oc1c(cccc2)c2ccc1 PAOWERWJVKTKID-UHFFFAOYSA-N 0.000 description 1
- FXIKHEAFIQZHDG-UHFFFAOYSA-N c(cc1)cc(cc2)c1cc2-c(ccc1c2)cc1ccc2-c(cc1)c(cccc2)c2c1Oc1c(cccc2)c2ccc1 Chemical compound c(cc1)cc(cc2)c1cc2-c(ccc1c2)cc1ccc2-c(cc1)c(cccc2)c2c1Oc1c(cccc2)c2ccc1 FXIKHEAFIQZHDG-UHFFFAOYSA-N 0.000 description 1
- RBVBLQVTBRIMON-UHFFFAOYSA-N c1ccc(cc(cc2)-c(cc3)cc4c3c(ccc(-c(c3c5cccc3)c(cccc3)c3c5Oc3c(cccc5)c5ccc3)c3)c3[o]4)c2c1 Chemical compound c1ccc(cc(cc2)-c(cc3)cc4c3c(ccc(-c(c3c5cccc3)c(cccc3)c3c5Oc3c(cccc5)c5ccc3)c3)c3[o]4)c2c1 RBVBLQVTBRIMON-UHFFFAOYSA-N 0.000 description 1
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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
- H10K85/615—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
- H10K85/626—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing more than one polycyclic condensed aromatic rings, e.g. bis-anthracene
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- 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
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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 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
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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
- H10K85/633—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
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1007—Non-condensed systems
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1003—Carbocyclic compounds
- C09K2211/1014—Carbocyclic compounds bridged by heteroatoms, e.g. N, P, Si or B
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1029—Heterocyclic compounds characterised by ligands containing one nitrogen atom as the heteroatom
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1088—Heterocyclic compounds characterised by ligands containing oxygen as the only heteroatom
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- C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
- C09K2211/10—Non-macromolecular compounds
- C09K2211/1018—Heterocyclic compounds
- C09K2211/1025—Heterocyclic compounds characterised by ligands
- C09K2211/1092—Heterocyclic compounds characterised by ligands containing sulfur as the only heteroatom
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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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- 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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- H10K50/00—Organic light-emitting devices
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- H10K50/14—Carrier transporting layers
- H10K50/15—Hole transporting layers
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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
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- Y02E10/00—Energy generation through renewable energy sources
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- Y02E10/52—PV systems with concentrators
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- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
- Y02E10/549—Organic PV cells
Definitions
- Ar 1 is a halogen group, C 1 -C 60 alkyl group, C 1 -C 60 alkoxy group, C 1 -C 60 alkylamine group, C 6 -C 60 arylamine group, C 1 -C 60 Alkylthiophene group, C 6 -C 60 aryl thiophene group, C 2 -C 60 alkenyl group, C 2 -C 60 alkynyl group, C 3 -C 60 cycloalkyl group, C 6 -C 60 aryl A group, a C 6 to C 60 aryl group substituted with deuterium, a C 8 to C 60 arylalkenyl group, a substituted or unsubstituted silane group, a substituted or unsubstituted boron group, a substituted or unsubstituted germanium group, and an aryl group, a substituted or unsubstituted substituted
- R ′ and R ′′ in Formulas 2 to 8 are the same as or different from each other, and each independently hydrogen; heavy hydrogen; Halogen, C One ⁇ C 60 Alkyl group, C 2 ⁇ C 60 Alkenyl, C One ⁇ C 60 Alkoxy group, C 6 ⁇ C 60 Aryl group, C 8 ⁇ C 60 Aryl alkenyl group, substituted or unsubstituted arylalkyl group, substituted or unsubstituted C 5 ⁇ C 60 C unsubstituted or substituted with one or more groups selected from the group consisting of a heterocyclic group, a nitrile group and an acetylene group One ⁇ C 50 of Alkyl groups; Halogen, C One ⁇ C 60 Alkyl group, C One ⁇ C 60 Alkoxy group, C 2 ⁇ C 60 Alkenyl, C 2 ⁇ C 60 Alkynyl, C 6 ⁇ C 60 Aryl group, C 8 ⁇ C 60 Aryl alkenyl group, substituted or
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- Materials Engineering (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Optics & Photonics (AREA)
- Organic Chemistry (AREA)
- Electroluminescent Light Sources (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Abstract
La présente invention concerne un composé, un élément électronique organique à l'aide de celui-ci et un dispositif électronique associé.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
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KR1020110040649A KR101123047B1 (ko) | 2011-04-29 | 2011-04-29 | 화합물 및 이를 이용한 유기전기소자, 그 전자장치 |
KR10-2011-0040649 | 2011-04-29 |
Publications (2)
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WO2012148127A2 true WO2012148127A2 (fr) | 2012-11-01 |
WO2012148127A3 WO2012148127A3 (fr) | 2013-01-10 |
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PCT/KR2012/002990 WO2012148127A2 (fr) | 2011-04-29 | 2012-04-19 | Composé, élément électronique organique l'utilisant et dispositif électronique associé |
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WO (1) | WO2012148127A2 (fr) |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013118846A1 (fr) * | 2012-02-10 | 2013-08-15 | 出光興産株式会社 | Dérivé d'amine aromatique, élément électroluminescent organique et dispositif électronique |
CN105384613A (zh) * | 2015-12-22 | 2016-03-09 | 吉林奥来德光电材料股份有限公司 | 一种新的有机电致发光材料及其制备方法和应用 |
JP2016103639A (ja) * | 2014-10-28 | 2016-06-02 | 三星ディスプレイ株式會社Samsung Display Co.,Ltd. | 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 |
CN107445886A (zh) * | 2017-05-24 | 2017-12-08 | 北京八亿时空液晶科技股份有限公司 | 一种高纯度3‑溴‑9‑苯基咔唑的制备方法 |
JP2019127487A (ja) * | 2018-01-26 | 2019-08-01 | 三星ディスプレイ株式會社Samsung Display Co.,Ltd. | 有機電界発光素子及び有機電界発光素子用モノアミン化合物 |
JP2019135228A (ja) * | 2018-01-26 | 2019-08-15 | 三星ディスプレイ株式會社Samsung Display Co.,Ltd. | 有機電界発光素子及び有機電界発光素子用モノアミン化合物 |
US11849632B2 (en) | 2019-03-20 | 2023-12-19 | Samsung Display Co., Ltd. | Amine-based compound and organic light-emitting device including the same |
US11871656B2 (en) | 2018-01-26 | 2024-01-09 | Samsung Display Co., Ltd. | Organic electroluminescence device and monoamine compound for organic electroluminescence device |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US9312500B2 (en) | 2012-08-31 | 2016-04-12 | Idemitsu Kosan Co., Ltd. | Organic electroluminescence device |
KR102140677B1 (ko) * | 2018-06-08 | 2020-08-03 | 주식회사 트리엘 | 신규한 유기발광소자용 화합물 및 이를 포함하는 유기막 재료용 코팅액 조성물 |
JP7456076B2 (ja) * | 2019-09-30 | 2024-03-27 | 国立大学法人群馬大学 | 化合物、化合物の製造方法、及び有機発光素子 |
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2011
- 2011-04-29 KR KR1020110040649A patent/KR101123047B1/ko active IP Right Grant
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2012
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JP2006056840A (ja) * | 2004-08-23 | 2006-03-02 | Mitsui Chemicals Inc | アントラセン化合物、および該アントラセン化合物を含有する有機電界発光素子 |
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KR20100039369A (ko) * | 2007-07-07 | 2010-04-15 | 이데미쓰 고산 가부시키가이샤 | 유기 일렉트로 루미네선스 소자 및 유기 일렉트로 루미네선스 소자용 재료 |
KR20090107208A (ko) * | 2008-04-08 | 2009-10-13 | 동우 화인켐 주식회사 | 나프탈렌 유도체, 이를 이용하는 유기전기발광소자용유기박막재료 및 이를 이용한 유기전기발광소자 |
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Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2013118846A1 (fr) * | 2012-02-10 | 2013-08-15 | 出光興産株式会社 | Dérivé d'amine aromatique, élément électroluminescent organique et dispositif électronique |
US9871203B2 (en) | 2012-02-10 | 2018-01-16 | Idemitsu Kosan Co., Ltd. | Aromatic amine derivative, organic electroluminescent element and electronic device |
US20160197283A1 (en) * | 2014-10-28 | 2016-07-07 | Samsung Display Co., Ltd. | Material for organic electroluminescent device and organic electroluminescent device including the same |
JP2016103639A (ja) * | 2014-10-28 | 2016-06-02 | 三星ディスプレイ株式會社Samsung Display Co.,Ltd. | 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 |
US9590186B2 (en) | 2014-10-28 | 2017-03-07 | Samsung Display Co., Ltd. | Material for organic electroluminescent device and organic electroluminescent device including the same |
US11050025B2 (en) | 2014-10-28 | 2021-06-29 | Samsung Display Co., Ltd. | Material for organic electroluminescent device and organic electroluminescent device including the same |
CN105384613A (zh) * | 2015-12-22 | 2016-03-09 | 吉林奥来德光电材料股份有限公司 | 一种新的有机电致发光材料及其制备方法和应用 |
CN107445886A (zh) * | 2017-05-24 | 2017-12-08 | 北京八亿时空液晶科技股份有限公司 | 一种高纯度3‑溴‑9‑苯基咔唑的制备方法 |
CN107445886B (zh) * | 2017-05-24 | 2020-02-21 | 北京八亿时空液晶科技股份有限公司 | 一种高纯度3-溴-9-苯基咔唑的制备方法 |
JP2019127487A (ja) * | 2018-01-26 | 2019-08-01 | 三星ディスプレイ株式會社Samsung Display Co.,Ltd. | 有機電界発光素子及び有機電界発光素子用モノアミン化合物 |
JP2019135228A (ja) * | 2018-01-26 | 2019-08-15 | 三星ディスプレイ株式會社Samsung Display Co.,Ltd. | 有機電界発光素子及び有機電界発光素子用モノアミン化合物 |
US11805697B2 (en) | 2018-01-26 | 2023-10-31 | Samsung Display Co., Ltd. | Organic electroluminescence device and monoamine compound for organic electroluminescence device |
US11871656B2 (en) | 2018-01-26 | 2024-01-09 | Samsung Display Co., Ltd. | Organic electroluminescence device and monoamine compound for organic electroluminescence device |
JP7465062B2 (ja) | 2018-01-26 | 2024-04-10 | 三星ディスプレイ株式會社 | 有機電界発光素子及び有機電界発光素子用モノアミン化合物 |
US11849632B2 (en) | 2019-03-20 | 2023-12-19 | Samsung Display Co., Ltd. | Amine-based compound and organic light-emitting device including the same |
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KR101123047B1 (ko) | 2012-03-16 |
WO2012148127A3 (fr) | 2013-01-10 |
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