WO2009066641A1 - 縮合芳香族誘導体及びそれを用いた有機エレクトロルミネッセンス素子 - Google Patents

縮合芳香族誘導体及びそれを用いた有機エレクトロルミネッセンス素子 Download PDF

Info

Publication number
WO2009066641A1
WO2009066641A1 PCT/JP2008/070882 JP2008070882W WO2009066641A1 WO 2009066641 A1 WO2009066641 A1 WO 2009066641A1 JP 2008070882 W JP2008070882 W JP 2008070882W WO 2009066641 A1 WO2009066641 A1 WO 2009066641A1
Authority
WO
WIPO (PCT)
Prior art keywords
same
fused aromatic
substituted
group
aromatic derivative
Prior art date
Application number
PCT/JP2008/070882
Other languages
English (en)
French (fr)
Inventor
Masahiro Kawamura
Original Assignee
Idemitsu Kosan Co., Ltd.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Idemitsu Kosan Co., Ltd. filed Critical Idemitsu Kosan Co., Ltd.
Priority to JP2009542548A priority Critical patent/JP5399920B2/ja
Priority to EP08851689.3A priority patent/EP2213641B1/en
Priority to US12/743,815 priority patent/US8623520B2/en
Publication of WO2009066641A1 publication Critical patent/WO2009066641A1/ja
Priority to US14/065,096 priority patent/US10153450B2/en

Links

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
    • H10K85/615—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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C15/00—Cyclic hydrocarbons containing only six-membered aromatic rings as cyclic parts
    • C07C15/20—Polycyclic condensed hydrocarbons
    • C07C15/38—Polycyclic condensed hydrocarbons containing four rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
    • C07F7/02—Silicon compounds
    • C07F7/08—Compounds having one or more C—Si linkages
    • C07F7/0803—Compounds with Si-C or Si-Si linkages
    • C07F7/0805—Compounds with Si-C or Si-Si linkages comprising only Si, C or H atoms
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B1/00—Dyes with anthracene nucleus not condensed with any other ring
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B57/00—Other synthetic dyes of known constitution
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B57/00—Other synthetic dyes of known constitution
    • C09B57/001—Pyrene dyes
    • 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
    • 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]
    • H10K50/11—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
    • H10K50/12—OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers comprising dopants
    • 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
    • H10K85/622—Polycyclic condensed aromatic hydrocarbons, e.g. anthracene containing four rings, e.g. pyrene
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00—Systems containing at least three condensed rings
    • C07C2603/02—Ortho- or ortho- and peri-condensed systems
    • C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
    • C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
    • C07C2603/24—Anthracenes; Hydrogenated anthracenes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00—Systems containing at least three condensed rings
    • C07C2603/02—Ortho- or ortho- and peri-condensed systems
    • C07C2603/04—Ortho- or ortho- and peri-condensed systems containing three rings
    • C07C2603/22—Ortho- or ortho- and peri-condensed systems containing three rings containing only six-membered rings
    • C07C2603/26—Phenanthrenes; Hydrogenated phenanthrenes
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2603/00—Systems containing at least three condensed rings
    • C07C2603/02—Ortho- or ortho- and peri-condensed systems
    • C07C2603/40—Ortho- or ortho- and peri-condensed systems containing four condensed rings
    • C07C2603/42—Ortho- or ortho- and peri-condensed systems containing four condensed rings containing only six-membered rings
    • 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
    • C09K2211/00—Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10—Non-macromolecular compounds
    • C09K2211/1003—Carbocyclic compounds
    • C09K2211/1011—Condensed systems
    • 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

Abstract

　下記式（１）で表される縮合芳香族誘導体。 （式（１）において、Ｒａ及びＲｂはそれぞれ水素原子又は置換基を表し、ｐは１～８の整数、ｑは１～１１の整数を表す。ｐ及びｑが２以上の場合、Ｒａ及びＲｂはそれぞれ同一でも異なっていてもよく、さらにＲａは隣接する置換基同士で環を形成してもよい。Ｌ１は単結合又は、置換もしくは無置換の２価の連結基を表す。Ａｒ１は、置換もしくは無置換の核炭素数６～５０のアリール基、又は、置換もしくは無置換の核原子数５～５０のヘテロアリール基を表す。ただし、Ｌ１が単結合であり、かつ、Ｒａの少なくとも１つが水素原子ではない場合、Ａｒ１はトリフェニレニル基ではない。また、Ｌ１及びＡｒ１の置換基、並びにＲａ及びＲｂはアミノ基を含まない。）
PCT/JP2008/070882 2007-11-21 2008-11-17 縮合芳香族誘導体及びそれを用いた有機エレクトロルミネッセンス素子 WO2009066641A1 (ja)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2009542548A JP5399920B2 (ja) 2007-11-21 2008-11-17 縮合芳香族誘導体及びそれを用いた有機エレクトロルミネッセンス素子
EP08851689.3A EP2213641B1 (en) 2007-11-21 2008-11-17 Fused aromatic derivative and organic electroluminescent device using the same
US12/743,815 US8623520B2 (en) 2007-11-21 2008-11-17 Fused aromatic derivative and organic electroluminescence device using the same
US14/065,096 US10153450B2 (en) 2007-11-21 2013-10-28 Fused aromatic derivative and organic electroluminescence device using the same

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2007301837 2007-11-21
JP2007-301837 2007-11-21

Related Child Applications (2)

Application Number Title Priority Date Filing Date
US12/743,815 A-371-Of-International US8623520B2 (en) 2007-11-21 2008-11-17 Fused aromatic derivative and organic electroluminescence device using the same
US14/065,096 Continuation US10153450B2 (en) 2007-11-21 2013-10-28 Fused aromatic derivative and organic electroluminescence device using the same

Publications (1)

Publication Number Publication Date
WO2009066641A1 true WO2009066641A1 (ja) 2009-05-28

Family

ID=40667463

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2008/070882 WO2009066641A1 (ja) 2007-11-21 2008-11-17 縮合芳香族誘導体及びそれを用いた有機エレクトロルミネッセンス素子

Country Status (6)

Country Link
US (2) US8623520B2 (ja)
EP (1) EP2213641B1 (ja)
JP (1) JP5399920B2 (ja)
KR (1) KR101477844B1 (ja)
TW (1) TW200927880A (ja)
WO (1) WO2009066641A1 (ja)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010013676A1 (ja) * 2008-07-28 2010-02-04 出光興産株式会社 有機発光媒体及び有機ｅｌ素子
WO2010013675A1 (ja) * 2008-07-28 2010-02-04 出光興産株式会社 有機発光媒体及び有機ｅｌ素子
JP2011504492A (ja) * 2007-11-22 2011-02-10 グラセル・ディスプレイ・インコーポレーテッド 高効率の青色電界発光化合物およびこれを使用する表示素子
JP2011157359A (ja) * 2010-02-03 2011-08-18 National Tsinghua Univ トリフェニレンベースの芳香族化合物およびそれを用いた有機発光ダイオード
WO2011137157A1 (en) * 2010-04-28 2011-11-03 Universal Display Corporation Triphenylene-benzofuran/benzothiophene/benzoselenophene compounds with substituents joining to form fused rings
CN102241620A (zh) * 2010-05-14 2011-11-16 国立清华大学 含苯并[9，10]菲基的芳香族化合物及利用其的有机发光二极管
WO2012014822A1 (ja) * 2010-07-29 2012-02-02 富士フイルム株式会社 有機電界発光素子及び電荷輸送材料
JP2013510104A (ja) * 2009-11-06 2013-03-21 メルク パテント ゲーエムベーハー 電子素子のための材料

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8623520B2 (en) * 2007-11-21 2014-01-07 Idemitsu Kosan Co., Ltd. Fused aromatic derivative and organic electroluminescence device using the same
CN101910147B (zh) 2007-12-28 2014-02-19 出光兴产株式会社 芳胺衍生物及使用该芳胺衍生物的有机电致发光元件
EP2271938B1 (en) * 2008-04-11 2014-02-26 Board of Regents of the University of Texas System Method and apparatus for nanoparticle electrogenerated chemiluminescence amplification
AU2009244904B2 (en) 2008-05-08 2014-04-17 Board Of Regents Of The University Of Texas System Luminescent nanostructured materials for use in electrogenerated chemiluminescence
EP2423206B1 (en) 2009-04-24 2014-01-08 Idemitsu Kosan Co., Ltd. Aromatic amine derivative, and organic electroluminescent element comprising same
KR101358494B1 (ko) 2009-12-16 2014-02-05 이데미쓰 고산 가부시키가이샤 방향족 아민 유도체 및 그것을 이용한 유기 전계 발광 소자
US8288015B2 (en) * 2010-04-18 2012-10-16 National Tsing Hua University Triphenylene based aromatic compounds and OLEDs utilizing the same
JP5973762B2 (ja) * 2011-03-31 2016-08-23 ユー・ディー・シー アイルランド リミテッド 電荷輸送材料、有機電界発光素子及び該素子を用いたことを特徴とする発光装置、表示装置または照明装置
KR101535824B1 (ko) * 2011-12-16 2015-07-13 엘지디스플레이 주식회사 유기 발광 소자
KR101433822B1 (ko) 2013-06-17 2014-08-27 삼성디스플레이 주식회사 유기 발광 장치
WO2015139808A1 (de) * 2014-03-18 2015-09-24 Merck Patent Gmbh Organische elektrolumineszenzvorrichtung
EP3196187A4 (en) 2014-09-19 2018-04-18 Idemitsu Kosan Co., Ltd Novel compound
KR20230117645A (ko) 2017-04-26 2023-08-08 오티아이 루미오닉스 인크. 표면의 코팅을 패턴화하는 방법 및 패턴화된 코팅을포함하는 장치
US11751415B2 (en) 2018-02-02 2023-09-05 Oti Lumionics Inc. Materials for forming a nucleation-inhibiting coating and devices incorporating same
CN113785411B (zh) 2019-03-07 2023-04-11 Oti照明公司 用于形成成核抑制涂层的材料和结合所述成核抑制涂层的装置

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003109765A (ja) * 2001-09-28 2003-04-11 Canon Inc 有機発光素子
JP2004059535A (ja) 2002-07-31 2004-02-26 Idemitsu Kosan Co Ltd アントラセン誘導体、有機エレクトロルミネッセンス素子用発光材料及び有機エレクトロルミネッセンス素子
JP2004139957A (ja) 2002-10-16 2004-05-13 National Tsinghua Univ 有機発光ダイオード
JP2006151844A (ja) 2004-11-26 2006-06-15 Canon Inc アミノアントリル誘導基置換化合物および有機発光素子
WO2008094399A1 (en) * 2007-01-30 2008-08-07 Eastman Kodak Company Oleds having high efficiency and excellent lifetime

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6150042A (en) 1996-12-09 2000-11-21 Toyo Ink Manufacturing Co., Ltd. Material for organoelectro-luminescence device and use thereof
CN1208422C (zh) * 1999-09-21 2005-06-29 出光兴产株式会社 有机电致发光装置和有机发光介质
JP2004002351A (ja) * 2002-03-27 2004-01-08 Tdk Corp 有機ｅｌ素子
JP4170655B2 (ja) * 2002-04-17 2008-10-22 出光興産株式会社 新規芳香族化合物及びそれを利用した有機エレクトロルミネッセンス素子
TWI314947B (en) * 2002-04-24 2009-09-21 Eastman Kodak Compan Organic light emitting diode devices with improved operational stability
ATE555182T1 (de) 2002-08-23 2012-05-15 Idemitsu Kosan Co Organische elektrolumineszenz vorrichtung und anthracenderivat
JP4035482B2 (ja) * 2003-06-27 2008-01-23 キヤノン株式会社 置換アントリル誘導体およびそれを使用した有機発光素子
JP4070676B2 (ja) 2003-07-25 2008-04-02 三井化学株式会社 非対称置換アントラセン化合物、および該非対称置換アントラセン化合物を含有する有機電界発光素子
WO2006003842A1 (ja) 2004-07-02 2006-01-12 Chisso Corporation 発光材料およびこれを用いた有機電界発光素子
US20060204783A1 (en) * 2005-03-10 2006-09-14 Conley Scott R Organic electroluminescent device
US20060286405A1 (en) * 2005-06-17 2006-12-21 Eastman Kodak Company Organic element for low voltage electroluminescent devices
JP4726584B2 (ja) * 2005-09-15 2011-07-20 三井化学株式会社 芳香族化合物、該芳香族化合物を含有する有機電界発光素子
US9666826B2 (en) * 2005-11-30 2017-05-30 Global Oled Technology Llc Electroluminescent device including an anthracene derivative
JP4979247B2 (ja) * 2006-03-08 2012-07-18 三井化学株式会社 アントラセン化合物および該化合物を含有する有機電界発光素子
KR100833218B1 (ko) 2006-04-14 2008-05-28 주식회사 이엘엠 트리페닐렌 유도체 및 이를 이용한 유기 발광 다이오드
KR100857025B1 (ko) * 2006-05-22 2008-09-05 (주)그라쎌 고성능의 청색 발광 화합물 및 이를 함유하는 표시소자
US8623520B2 (en) * 2007-11-21 2014-01-07 Idemitsu Kosan Co., Ltd. Fused aromatic derivative and organic electroluminescence device using the same
WO2009066809A1 (en) * 2007-11-22 2009-05-28 Gracel Display Inc. Blue electroluminescent compounds with high efficiency and display device using the same
JP2009209127A (ja) * 2008-02-08 2009-09-17 Toyo Ink Mfg Co Ltd カルバゾリル基を有する化合物およびその用途
KR100910150B1 (ko) 2008-04-02 2009-08-03 (주)그라쎌 신규한 유기 발광 화합물 및 이를 발광재료로서 채용하고있는 유기 발광 소자

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003109765A (ja) * 2001-09-28 2003-04-11 Canon Inc 有機発光素子
JP2004059535A (ja) 2002-07-31 2004-02-26 Idemitsu Kosan Co Ltd アントラセン誘導体、有機エレクトロルミネッセンス素子用発光材料及び有機エレクトロルミネッセンス素子
JP2004139957A (ja) 2002-10-16 2004-05-13 National Tsinghua Univ 有機発光ダイオード
JP2006151844A (ja) 2004-11-26 2006-06-15 Canon Inc アミノアントリル誘導基置換化合物および有機発光素子
WO2008094399A1 (en) * 2007-01-30 2008-08-07 Eastman Kodak Company Oleds having high efficiency and excellent lifetime

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP2213641A4

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011504492A (ja) * 2007-11-22 2011-02-10 グラセル・ディスプレイ・インコーポレーテッド 高効率の青色電界発光化合物およびこれを使用する表示素子
WO2010013676A1 (ja) * 2008-07-28 2010-02-04 出光興産株式会社 有機発光媒体及び有機ｅｌ素子
WO2010013675A1 (ja) * 2008-07-28 2010-02-04 出光興産株式会社 有機発光媒体及び有機ｅｌ素子
JPWO2010013676A1 (ja) * 2008-07-28 2012-01-12 出光興産株式会社 有機発光媒体及び有機ｅｌ素子
JP2013510104A (ja) * 2009-11-06 2013-03-21 メルク パテント ゲーエムベーハー 電子素子のための材料
JP2011157359A (ja) * 2010-02-03 2011-08-18 National Tsinghua Univ トリフェニレンベースの芳香族化合物およびそれを用いた有機発光ダイオード
TWI397516B (zh) * 2010-02-03 2013-06-01 Nat Univ Tsing Hua 含聯三伸苯基之芳香族化合物及有機發光二極體
WO2011137157A1 (en) * 2010-04-28 2011-11-03 Universal Display Corporation Triphenylene-benzofuran/benzothiophene/benzoselenophene compounds with substituents joining to form fused rings
JP2013525446A (ja) * 2010-04-28 2013-06-20 ユニバーサル ディスプレイ コーポレイション 融合環を形成するために関与する置換基を持つ、トリフェニレン−ベンゾフラン／ベンゾチオフェン／ベンゾセレノフェン化合物
CN102241620A (zh) * 2010-05-14 2011-11-16 国立清华大学 含苯并[9，10]菲基的芳香族化合物及利用其的有机发光二极管
WO2012014822A1 (ja) * 2010-07-29 2012-02-02 富士フイルム株式会社 有機電界発光素子及び電荷輸送材料
JP2012089810A (ja) * 2010-07-29 2012-05-10 Fujifilm Corp 有機電界発光素子及び電荷輸送材料

Also Published As

Publication number Publication date
EP2213641A1 (en) 2010-08-04
KR20100090269A (ko) 2010-08-13
US10153450B2 (en) 2018-12-11
JP5399920B2 (ja) 2014-01-29
US20100295030A1 (en) 2010-11-25
JPWO2009066641A1 (ja) 2011-04-07
KR101477844B1 (ko) 2014-12-30
EP2213641B1 (en) 2018-05-16
US8623520B2 (en) 2014-01-07
TW200927880A (en) 2009-07-01
US20140061628A1 (en) 2014-03-06
EP2213641A4 (en) 2011-01-26

Similar Documents

Publication Publication Date Title
WO2009066641A1 (ja) 縮合芳香族誘導体及びそれを用いた有機エレクトロルミネッセンス素子
WO2009063846A1 (ja) ベンゾクリセン誘導体及びそれを用いた有機エレクトロルミネッセンス素子
WO2009069566A1 (ja) ベンゾフェナントレン誘導体及びそれを用いた有機エレクトロルミネッセンス素子
WO2009063833A1 (ja) ベンゾクリセン誘導体及びそれを用いた有機エレクトロルミネッセンス素子
WO2009069523A1 (ja) アミン系高分子化合物及びそれを用いた発光素子
WO2009054253A1 (ja) 有機エレクトロルミネッセンス素子、表示装置及び照明装置
EP1968131A4 (en) ORGANIC ELECTROLUMINESCENT DEVICE AND MATERIAL THEREFOR
EP2845587A3 (en) Melanin production inhibitor
WO2008123540A3 (en) Organic electroluminescent device
WO2009069736A1 (ja) 含窒素化合物
WO2008129912A1 (ja) フェニル基置換１，３，５－トリアジン化合物、その製造方法、およびこれを構成成分とする有機電界発光素子
RS54146B1 (en) CIKLOPENTILAKRILAMIDA DERIVATIVES
TW200726749A (en) Diaminoarylene compound having carbazolyl group and use thereof
TW200722422A (en) Heterocyclic compound and organic electroluminescent device using the same
DE60212668D1 (de) Halbleiter auf basis von substituiertem pentacen
TW201129673A (en) Aromatic amine derivative and organic electroluminescent element using same
WO2008146665A1 (ja) 有機エレクトロルミネッセンス素子用材料及び有機エレクトロルミネッセンス素子並びに有機エレクトロルミネッセンス表示装置
WO2008114817A1 (ja) 新規なアデニン化合物
WO2009066600A1 (ja) モノベンゾクリセン誘導体、及びそれを含む有機エレクトロルミネッセンス素子用材料、並びにそれを用いた有機エレクトロルミネッセンス素子
TW200704668A (en) Aromatic polymer
TW200736230A (en) Organic compound, charge transporting material, charge transporting material composition and organic electroluminescent element
MX2010003156A (es) Derivados de aril amida substituida con tetrazol y usos de los mismos.
TW200739260A (en) Diketoxime ester compound and use thererof
WO2008126890A1 (ja) ヒドラジド化合物およびそれを含有する有害節足動物防除剤
TN2010000061A1 (en) Tricyclic bridged cyclopentanedione derivatives as herbicides

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 08851689

Country of ref document: EP

Kind code of ref document: A1

WWE Wipo information: entry into national phase

Ref document number: 2009542548

Country of ref document: JP

WWE Wipo information: entry into national phase

Ref document number: 2008851689

Country of ref document: EP

ENP Entry into the national phase

Ref document number: 20107011034

Country of ref document: KR

Kind code of ref document: A

NENP Non-entry into the national phase

Ref country code: DE

WWE Wipo information: entry into national phase

Ref document number: 12743815

Country of ref document: US