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芳基取代蒽衍生物的合成及发光性能研究

吕宏飞 张惠 杨杰 吴绵园 李猛 徐虹 白雪峰

液晶与显示2016,Vol.31Issue(12):1105-1111,7.
液晶与显示2016,Vol.31Issue(12):1105-1111,7.DOI:10.3788/YJYXS20163112.1105

芳基取代蒽衍生物的合成及发光性能研究

Synthesis and properties of anthracene derivatives using as electroluminescent materials in OLEDs

吕宏飞 1张惠 1杨杰 1吴绵园 1李猛 1徐虹 1白雪峰1

作者信息

  • 1. 黑龙江省科学院 石油化学研究院,黑龙江 哈尔滨 150040
  • 折叠

摘要

Abstract

9-(4-(naphthalen-1-yl )phenyl )-10-(naphthalen-2-yl )anthracene (NAPA-1 ) and 9-(naphthalen-2-yl)-10-(4-(naphthalen-2-yl)phenyl)anthracene(NAPA-2)are synthesized starting from 9-bromo-10-(naphthalen-2-yl)anthracene,4-(naphthalene-1-yl)phenylboronic acid and 4-(naphthalen-2-yl)phenylboronic acid by Suzuki coupling reaction.Structures of the target compounds are character-ized by IR,NMR.Results of TG and DSC analysis show the compounds have good thermal stability. The PL spectra of NAPA-1 and NAPA-2 in solution were found to exhibit excellent blue emission with the peak maxima at λmax = 424 nm,428 nm respectively.NAPA-1 and NAPA-2 have excellent light emitting performance and could be used as materials for organic light emitting diodes (OLEDs).

关键词

有机电致发光/芳基蒽/铃木偶联/蓝光材料

Key words

organic electroluminescent/arylanthracene/Suzuki coupling/Blue light-emitting materi-als

分类

信息技术与安全科学

引用本文复制引用

吕宏飞,张惠,杨杰,吴绵园,李猛,徐虹,白雪峰..芳基取代蒽衍生物的合成及发光性能研究[J].液晶与显示,2016,31(12):1105-1111,7.

基金项目

黑龙江省哈尔滨市科技攻关项目(No.2011AA4AG066) Supported by Harbin Programs for Science and Technology Development(No.2011AA4AG066) (No.2011AA4AG066)

液晶与显示

OA北大核心CSCDCSTPCD

1007-2780

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