JP2009137941A5 - - Google Patents

Download PDF

Info

Publication number
JP2009137941A5
JP2009137941A5 JP2008281102A JP2008281102A JP2009137941A5 JP 2009137941 A5 JP2009137941 A5 JP 2009137941A5 JP 2008281102 A JP2008281102 A JP 2008281102A JP 2008281102 A JP2008281102 A JP 2008281102A JP 2009137941 A5 JP2009137941 A5 JP 2009137941A5
Authority
JP
Japan
Prior art keywords
alkyl
tri
halogen
arylsilyl
aryl
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.)
Granted
Application number
JP2008281102A
Other languages
English (en)
Japanese (ja)
Other versions
JP5554914B2 (ja
JP2009137941A (ja
Filing date
Publication date
Priority claimed from KR1020070111837A external-priority patent/KR100923571B1/ko
Application filed filed Critical
Publication of JP2009137941A publication Critical patent/JP2009137941A/ja
Publication of JP2009137941A5 publication Critical patent/JP2009137941A5/ja
Application granted granted Critical
Publication of JP5554914B2 publication Critical patent/JP5554914B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

JP2008281102A 2007-11-05 2008-10-31 新規な有機エレクトロルミネセント化合物及びこれを使用する有機エレクトロルミネセントデバイス Expired - Fee Related JP5554914B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR10-2007-0111837 2007-11-05
KR1020070111837A KR100923571B1 (ko) 2007-11-05 2007-11-05 신규한 적색 인광 화합물 및 이를 발광재료로서 채용하고있는 유기발광소자

Publications (3)

Publication Number Publication Date
JP2009137941A JP2009137941A (ja) 2009-06-25
JP2009137941A5 true JP2009137941A5 (enExample) 2014-01-16
JP5554914B2 JP5554914B2 (ja) 2014-07-23

Family

ID=40263301

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008281102A Expired - Fee Related JP5554914B2 (ja) 2007-11-05 2008-10-31 新規な有機エレクトロルミネセント化合物及びこれを使用する有機エレクトロルミネセントデバイス

Country Status (6)

Country Link
US (1) US20090153037A1 (enExample)
EP (1) EP2055710A1 (enExample)
JP (1) JP5554914B2 (enExample)
KR (1) KR100923571B1 (enExample)
CN (1) CN101508705B (enExample)
TW (1) TW200946634A (enExample)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9130177B2 (en) * 2011-01-13 2015-09-08 Universal Display Corporation 5-substituted 2 phenylquinoline complexes materials for light emitting diode
US8269317B2 (en) * 2010-11-11 2012-09-18 Universal Display Corporation Phosphorescent materials
US10008677B2 (en) 2011-01-13 2018-06-26 Universal Display Corporation Materials for organic light emitting diode
CN102942920A (zh) * 2012-11-15 2013-02-27 安徽工业大学 以三氟乙酰苯基取代喹啉为配体的铱配合物磷光材料及其制备方法
CN103450891A (zh) * 2013-09-24 2013-12-18 安徽工业大学 以氟代吡啶羧酸为辅助配体的铱配合物磷光材料及其制备方法
CN105814069A (zh) * 2013-12-12 2016-07-27 三菱化学株式会社 铱配位化合物及其制造方法、含有其的组合物、有机场致发光元件、显示装置和照明装置
US9929357B2 (en) * 2014-07-22 2018-03-27 Universal Display Corporation Organic electroluminescent materials and devices
KR102563713B1 (ko) 2017-04-26 2023-08-07 오티아이 루미오닉스 인크. 표면의 코팅을 패턴화하는 방법 및 패턴화된 코팅을 포함하는 장치
CN108017677A (zh) * 2017-12-12 2018-05-11 上海道亦化工科技有限公司 一种铱配合物及其用途和有机电致发光器件
US11751415B2 (en) 2018-02-02 2023-09-05 Oti Lumionics Inc. Materials for forming a nucleation-inhibiting coating and devices incorporating same
KR20250160226A (ko) 2019-03-07 2025-11-11 오티아이 루미오닉스 인크. 핵생성 억제 코팅물 형성용 재료 및 이를 포함하는 디바이스
JP7555600B2 (ja) 2019-04-18 2024-09-25 オーティーアイ ルミオニクス インコーポレーテッド 核生成抑制コーティングを形成するための材料およびそれを組み込んだデバイス
JP7576337B2 (ja) 2019-05-08 2024-11-01 オーティーアイ ルミオニクス インコーポレーテッド 核生成抑制コーティングを形成するための材料およびそれを組み込んだデバイス

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH1072581A (ja) 1995-09-25 1998-03-17 Toyo Ink Mfg Co Ltd 有機エレクトロルミネッセンス素子用発光材料およびそれを使用した有機エレクトロルミネッセンス素子
JP3929689B2 (ja) * 2000-03-28 2007-06-13 富士フイルム株式会社 高効率赤色発光素子、イリジウム錯体から成る発光素子材料及び新規イリジウム錯体
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
JP4048521B2 (ja) * 2000-05-02 2008-02-20 富士フイルム株式会社 発光素子
US6835469B2 (en) * 2001-10-17 2004-12-28 The University Of Southern California Phosphorescent compounds and devices comprising the same
JP3933591B2 (ja) * 2002-03-26 2007-06-20 淳二 城戸 有機エレクトロルミネッセント素子
KR100509603B1 (ko) * 2002-12-28 2005-08-22 삼성에스디아이 주식회사 적색 발광 화합물 및 이를 채용한 유기 전계 발광 소자
WO2005003095A1 (ja) * 2003-07-02 2005-01-13 Idemitsu Kosan Co., Ltd. 金属錯体化合物及びそれを用いた有機エレクトロルミネッセンス素子
JP4478555B2 (ja) * 2004-11-30 2010-06-09 キヤノン株式会社 金属錯体、発光素子及び画像表示装置
KR100788262B1 (ko) * 2006-02-27 2007-12-27 (주)그라쎌 적색 발광 화합물 및 이를 발광재료로서 채용하고 있는발광소자
TWI510598B (zh) * 2007-03-08 2015-12-01 Universal Display Corp 磷光材料

Similar Documents

Publication Publication Date Title
JP2009149638A5 (enExample)
Du et al. Os (II) based green to red phosphors: A great prospect for solution‐processed, highly efficient organic light‐emitting diodes
JP2009218571A5 (enExample)
EP2182002B1 (en) Novel compounds for electronic material and organic electronic device using the same
Li et al. Rational design and characterization of heteroleptic phosphorescent complexes for highly efficient deep-red organic light-emitting devices
Volz et al. Molecular construction kit for tuning solubility, stability and luminescence properties: heteroleptic MePyrPHOS-copper iodide-complexes and their application in organic light-emitting diodes
Wei et al. Constructing lanthanide [Nd (III), Er (III) and Yb (III)] complexes using a tridentate N, N, O-ligand for near-infrared organic light-emitting diodes
Ionkin et al. Syntheses, Structural Characterization, and First Electroluminescent Properties of Mono-cyclometalated Platinum (II) Complexes with Greater than Classical π− π Stacking and Pt− Pt Distances
Shigehiro et al. Photo-and electroluminescence from 2-(dibenzo [b, d] furan-4-yl) pyridine-based heteroleptic cyclometalated platinum (II) complexes: excimer formation drastically facilitated by an aromatic diketonate ancillary ligand
Chan et al. Synthesis and characterization of luminescent cyclometalated platinum (II) complexes of 1, 3‐bis‐hetero‐azolylbenzenes with tunable color for applications in organic light‐emitting devices through extension of π conjugation by variation of the heteroatom
JP2012515730A5 (enExample)
JP2017031167A5 (enExample)
JP5554914B2 (ja) 新規な有機エレクトロルミネセント化合物及びこれを使用する有機エレクトロルミネセントデバイス
JP2009523146A5 (enExample)
JP2009191066A (ja) 新規な有機エレクトロルミネセント化合物及びこれを使用する有機エレクトロルミネセント素子
CA2417502A1 (en) Dye-sensitized photoelectric conversion device
JP2013539206A5 (enExample)
JP2009209142A (ja) 新規な有機エレクトロルミネセント化合物及びこれを使用する有機エレクトロルミネセント素子
You et al. A deep red phosphorescent Ir (III) complex for use in polymer light-emitting diodes: role of the arylsilyl substituents
KR100682859B1 (ko) 폴리실세스퀴옥산계 화합물 및 이를 이용한 유기 전계발광 소자
Arsenyan et al. Synthesis and performance in OLEDs of selenium-containing phosphorescent emitters with red emission color deeper than the corresponding NTSC standard
JP2013147449A (ja) 金属錯体及び該金属錯体を含む発光素子
Yan et al. Methoxyl modification in furo [3, 2-c] pyridine-based iridium complexes towards highly efficient green-and orange-emitting electrophosphorescent devices
Hao et al. Dual phosphorescence emission of dinuclear platinum (II) complex incorporating cyclometallating pyrenyl-dipyridine-based ligand and its application in near-infrared solution-processed polymer light-emitting diodes
Zhao et al. Novel bluish green benzimidazole-based iridium (iii) complexes for highly efficient phosphorescent organic light-emitting diodes