TW200540249A - 2,4,5-triaryl substituted imidazole compound and 1,2,4,5-tetraaryl substituted imidazole compound - Google Patents

2,4,5-triaryl substituted imidazole compound and 1,2,4,5-tetraaryl substituted imidazole compound Download PDF

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Publication number
TW200540249A
TW200540249A TW094106830A TW94106830A TW200540249A TW 200540249 A TW200540249 A TW 200540249A TW 094106830 A TW094106830 A TW 094106830A TW 94106830 A TW94106830 A TW 94106830A TW 200540249 A TW200540249 A TW 200540249A
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TW
Taiwan
Prior art keywords
group
phenyl
atom
biphenyl
optionally substituted
Prior art date
Application number
TW094106830A
Other languages
English (en)
Chinese (zh)
Inventor
Shuntaro Mataka
Taizo Hatta
Original Assignee
Nissan Chemical Ind Ltd
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Filing date
Publication date
Application filed by Nissan Chemical Ind Ltd filed Critical Nissan Chemical Ind Ltd
Publication of TW200540249A publication Critical patent/TW200540249A/zh

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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K11/00Luminescent, e.g. electroluminescent, chemiluminescent materials
    • C09K11/06Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05BELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B33/00Electroluminescent light sources
    • H05B33/12Light sources with substantially two-dimensional radiating surfaces
    • H05B33/14Light 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
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60Organic compounds having low molecular weight
    • H10K85/649Aromatic compounds comprising a hetero atom
    • H10K85/654Aromatic compounds comprising a hetero atom comprising only nitrogen as heteroatom
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K2211/00Chemical nature of organic luminescent or tenebrescent compounds
    • C09K2211/10Non-macromolecular compounds
    • C09K2211/1018Heterocyclic compounds
    • C09K2211/1025Heterocyclic compounds characterised by ligands
    • C09K2211/1044Heterocyclic compounds characterised by ligands containing two nitrogen atoms as heteroatoms
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K50/00Organic light-emitting devices
    • H10K50/10OLEDs or polymer light-emitting diodes [PLED]
    • H10K50/11OLEDs or polymer light-emitting diodes [PLED] characterised by the electroluminescent [EL] layers
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60Organic compounds having low molecular weight
    • H10K85/615Polycyclic condensed aromatic hydrocarbons, e.g. anthracene
    • HELECTRICITY
    • H10SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
    • H10KORGANIC ELECTRIC SOLID-STATE DEVICES
    • H10K85/00Organic materials used in the body or electrodes of devices covered by this subclass
    • H10K85/60Organic compounds having low molecular weight
    • H10K85/631Amine compounds having at least two aryl rest on at least one amine-nitrogen atom, e.g. triphenylamine
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E10/00Energy generation through renewable energy sources
    • Y02E10/50Photovoltaic [PV] energy
    • Y02E10/549Organic PV cells

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Organic Chemistry (AREA)
  • Electroluminescent Light Sources (AREA)
  • Hybrid Cells (AREA)
  • Plural Heterocyclic Compounds (AREA)
TW094106830A 2004-03-09 2005-03-07 2,4,5-triaryl substituted imidazole compound and 1,2,4,5-tetraaryl substituted imidazole compound TW200540249A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2004065342 2004-03-09

Publications (1)

Publication Number Publication Date
TW200540249A true TW200540249A (en) 2005-12-16

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Family Applications (1)

Application Number Title Priority Date Filing Date
TW094106830A TW200540249A (en) 2004-03-09 2005-03-07 2,4,5-triaryl substituted imidazole compound and 1,2,4,5-tetraaryl substituted imidazole compound

Country Status (3)

Country Link
JP (1) JPWO2005085208A1 (ja)
TW (1) TW200540249A (ja)
WO (1) WO2005085208A1 (ja)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2007111263A1 (ja) * 2006-03-27 2009-08-13 出光興産株式会社 含窒素複素環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
US20080090834A1 (en) * 2006-07-06 2008-04-17 Pfizer Inc Selective azole pde10a inhibitor compounds
CN101280196B (zh) * 2008-06-03 2011-01-26 西安近代化学研究所 四环液晶化合物
WO2014157371A1 (ja) * 2013-03-28 2014-10-02 日本合成化学工業株式会社 新規イミダゾール化合物、電子デバイス用材料、発光素子、電子デバイス及びその製造方法
CN104962277B (zh) * 2015-05-04 2017-05-24 四川大学 有机单分子白光材料双三苯胺取代邻羟基苯基唑类衍生物的制备及应用
CN106008467B (zh) * 2016-05-27 2019-01-22 上海道亦化工科技有限公司 一种基于咪唑的化合物及其有机电致发光器件
CN106607091B (zh) * 2016-10-10 2019-03-19 湘潭大学 微孔聚合物-纳米金属粒子催化剂及其制备方法和应用
CN112194630A (zh) * 2020-10-30 2021-01-08 南京林业大学 一种以咪唑衍生物为核的有机空穴传输材料的制备及应用
KR102638780B1 (ko) * 2021-10-29 2024-02-20 고려대학교 세종산학협력단 유기발광소자용 화합물, 그 제조방법 및 이를 구비하는 유기발광소자
US12006295B1 (en) 2023-11-08 2024-06-11 King Faisal University 4,5-bis(4-bromophenyl)-2-(4-bromophenyl)-1-hexyl-1H-imidazole as an antimicrobial compound

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3084079B2 (ja) * 1991-03-06 2000-09-04 マナック株式会社 ロフィン誘導体
JPH05117241A (ja) * 1991-09-13 1993-05-14 Ichikawa Tetsuya 4−ヒドロペルオキシ−2−(n,n−ジ置換アミノフエニル)−4,5−ジフエニル−4h−イソイミダゾール
JP4221129B2 (ja) * 1999-02-15 2009-02-12 富士フイルム株式会社 含窒素ヘテロ環化合物、有機発光素子材料、有機発光素子
JP3925265B2 (ja) * 2002-03-25 2007-06-06 コニカミノルタホールディングス株式会社 有機エレクトロルミネッセンス素子及びそれを用いた表示装置

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JPWO2005085208A1 (ja) 2007-12-13
WO2005085208A1 (ja) 2005-09-15

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