CN1876664A - 有机金属络合物以及使用其的有机电致发光器件 - Google Patents
有机金属络合物以及使用其的有机电致发光器件 Download PDFInfo
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- CN1876664A CN1876664A CNA200610071109XA CN200610071109A CN1876664A CN 1876664 A CN1876664 A CN 1876664A CN A200610071109X A CNA200610071109X A CN A200610071109XA CN 200610071109 A CN200610071109 A CN 200610071109A CN 1876664 A CN1876664 A CN 1876664A
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- Prior art keywords
- replace
- unsubstituted
- organometallic complex
- replacement
- atom
- Prior art date
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- -1 heterocyclic radical Chemical class 0.000 claims description 14
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 14
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- 229910052697 platinum Inorganic materials 0.000 claims description 8
- 125000004122 cyclic group Chemical group 0.000 claims description 7
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/16—Bone cutting, breaking or removal means other than saws, e.g. Osteoclasts; Drills or chisels for bones; Trepans
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/32—Surgical cutting instruments
- A61B17/320068—Surgical cutting instruments using mechanical vibrations, e.g. ultrasonic
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- 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
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- H—ELECTRICITY
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Abstract
Description
Claims (13)
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KR10182/05 | 2005-02-03 | ||
KR1020050010182A KR101234226B1 (ko) | 2005-02-03 | 2005-02-03 | 유기 금속 착물 및 이를 이용한 유기 전계 발광 소자 |
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US (1) | US7678473B2 (zh) |
JP (1) | JP5186085B2 (zh) |
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101186624B (zh) * | 2007-08-16 | 2012-09-05 | 清华大学 | 一种铱金属配合物及其应用 |
CN102844402A (zh) * | 2010-01-25 | 2012-12-26 | 欧司朗股份有限公司 | 磷光性的金属络合化合物、用于制造其的方法和发光器件 |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100809906B1 (ko) * | 2006-12-28 | 2008-03-06 | 주식회사 잉크테크 | 신규한 트리 아릴 아민계 화합물이 도입된 이리듐 인광덴드리머 화합물, 이의 제조 방법 및 이를 발광재료로채용하고 있는 유기전계발광소자 |
WO2008117633A1 (en) * | 2007-03-23 | 2008-10-02 | Semiconductor Energy Laboratory Co., Ltd. | Composition, method for fabricating light-emitting element, light-emitting element, light-emitting device, and electronic device |
WO2011024737A1 (ja) | 2009-08-27 | 2011-03-03 | 独立行政法人産業技術総合研究所 | イリジウム錯体ならびに該化合物からなる発光材料 |
WO2011024761A1 (ja) | 2009-08-27 | 2011-03-03 | 住友化学株式会社 | 金属錯体組成物及び錯体高分子 |
CN103907217B (zh) | 2011-09-12 | 2016-10-12 | 新日铁住金化学株式会社 | 有机电致发光元件 |
KR20140076572A (ko) | 2011-09-12 | 2014-06-20 | 신닛테츠 수미킨 가가쿠 가부시키가이샤 | 함규소 4원환구조를 가지는 유기전계발광 소자용 재료 및 유기전계발광 소자 |
CN103797602B (zh) | 2011-09-12 | 2016-03-23 | 新日铁住金化学株式会社 | 有机电致发光元件 |
JP6006732B2 (ja) | 2011-12-12 | 2016-10-12 | 新日鉄住金化学株式会社 | 有機電界発光素子用材料及びそれを用いた有機電界発光素子 |
US9985219B2 (en) | 2012-03-12 | 2018-05-29 | Nippon Steel & Sumikin Chemical Co., Ltd. | Organic electroluminescent element |
WO2014002629A1 (ja) | 2012-06-28 | 2014-01-03 | 新日鉄住金化学株式会社 | 有機電界発光素子用材料及び有機電界発光素子 |
CN104471734B (zh) | 2012-07-19 | 2016-11-09 | 新日铁住金化学株式会社 | 有机电场发光元件 |
TWI599570B (zh) | 2012-09-28 | 2017-09-21 | 新日鐵住金化學股份有限公司 | Compounds for organic electroluminescent devices and organic electroluminescent devices |
KR101802855B1 (ko) | 2015-11-30 | 2017-11-30 | 엘지디스플레이 주식회사 | 용액 공정이 가능한 저분자 발광 화합물, 발광 화합물을 포함하는 발광다이오드 및 표시장치 |
CN110264516A (zh) * | 2019-05-27 | 2019-09-20 | 山东科技大学 | 一种光线枪激光笔指向位置确定系统 |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20020121638A1 (en) | 2000-06-30 | 2002-09-05 | Vladimir Grushin | Electroluminescent iridium compounds with fluorinated phenylpyridines, phenylpyrimidines, and phenylquinolines and devices made with such compounds |
US6939624B2 (en) | 2000-08-11 | 2005-09-06 | Universal Display Corporation | Organometallic compounds and emission-shifting organic electrophosphorescence |
JP5241053B2 (ja) | 2000-08-11 | 2013-07-17 | ザ、トラスティーズ オブ プリンストン ユニバーシティ | 有機金属化合物及び放射移行有機電気燐光体 |
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 |
JP4154138B2 (ja) | 2000-09-26 | 2008-09-24 | キヤノン株式会社 | 発光素子、表示装置及び金属配位化合物 |
DE10109027A1 (de) * | 2001-02-24 | 2002-09-05 | Covion Organic Semiconductors | Rhodium- und Iridium-Komplexe |
KR100509603B1 (ko) * | 2002-12-28 | 2005-08-22 | 삼성에스디아이 주식회사 | 적색 발광 화합물 및 이를 채용한 유기 전계 발광 소자 |
JP4198654B2 (ja) * | 2003-08-07 | 2008-12-17 | 三星エスディアイ株式会社 | イリジウム化合物及びそれを採用した有機電界発光素子 |
KR101015882B1 (ko) * | 2004-10-11 | 2011-02-23 | 삼성모바일디스플레이주식회사 | 시클로메탈화 전이금속 착물 및 이를 이용한 유기 전계발광 소자 |
TWI282250B (en) * | 2005-04-21 | 2007-06-01 | Au Optronics Corp | Light emission material and organic electroluminescent device using the same |
-
2005
- 2005-02-03 KR KR1020050010182A patent/KR101234226B1/ko active IP Right Grant
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2006
- 2006-02-03 US US11/346,585 patent/US7678473B2/en active Active
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101186624B (zh) * | 2007-08-16 | 2012-09-05 | 清华大学 | 一种铱金属配合物及其应用 |
CN102844402A (zh) * | 2010-01-25 | 2012-12-26 | 欧司朗股份有限公司 | 磷光性的金属络合化合物、用于制造其的方法和发光器件 |
CN102844402B (zh) * | 2010-01-25 | 2016-06-22 | 欧司朗股份有限公司 | 磷光性的金属络合化合物、用于制造其的方法和发光器件 |
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KR101234226B1 (ko) | 2013-02-18 |
JP5186085B2 (ja) | 2013-04-17 |
JP2006213720A (ja) | 2006-08-17 |
KR20060089100A (ko) | 2006-08-08 |
CN1876664B (zh) | 2011-03-30 |
US7678473B2 (en) | 2010-03-16 |
US20060172150A1 (en) | 2006-08-03 |
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