中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
A facile synthesis of 2,3,6,7-tetrabromonaphthalene diimides toward new pi-extended naphthalene diimides

文献类型:期刊论文

作者Hu, Yunbin1; Wang, Zhongli1; Yang, Xiaodi3; Zhao, Zheng1; Han, Wenjie1; Yuan, Wei1; Li, Hongxiang1; Gao, Xike1; Zhu, Daoben1,2
刊名TETRAHEDRON LETTERS
出版日期2013-05-01
卷号54期号:18页码:2271-2273
关键词Synthetic Method Organic Semiconductor Naphthalene Diimide Anion-pi Interaction
ISSN号0040-4039
DOI10.1016/j.tetlet.2013.02.075
英文摘要A 2,3,6,7-tetrabromonaphthalene diimide (2) was readily synthesized in high yield from 2,3,6,7-tetrabromonaphthalene dianhydride by an improved dehydrohalogenation-based imidization reaction. The further nucleophilic aromatic substitution (SNAr) reaction of 2 with potassium cyanocarbonimidodithioate afforded a new pi-extended naphthalene diimide (1), which exhibits n-type behavior in organic transistors and interesting response to F- among halide anions in solutions. (C) 2013 Elsevier Ltd. All rights reserved.
语种英语
WOS记录号WOS:000317640800016
出版者PERGAMON-ELSEVIER SCIENCE LTD
源URL[http://ir.iccas.ac.cn/handle/121111/47019]  
专题中国科学院化学研究所
通讯作者Gao, Xike
作者单位1.Chinese Acad Sci, Mat Sci Lab, Shanghai Inst Organ Chem, Shanghai 200032, Peoples R China
2.Chinese Acad Sci, Beijing Natl Lab Mol Sci, Key Lab Organ Solids, Beijing 100190, Peoples R China
3.Fudan Univ, Adv Mat Lab, Shanghai 200433, Peoples R China
推荐引用方式
GB/T 7714
Hu, Yunbin,Wang, Zhongli,Yang, Xiaodi,et al. A facile synthesis of 2,3,6,7-tetrabromonaphthalene diimides toward new pi-extended naphthalene diimides[J]. TETRAHEDRON LETTERS,2013,54(18):2271-2273.
APA Hu, Yunbin.,Wang, Zhongli.,Yang, Xiaodi.,Zhao, Zheng.,Han, Wenjie.,...&Zhu, Daoben.(2013).A facile synthesis of 2,3,6,7-tetrabromonaphthalene diimides toward new pi-extended naphthalene diimides.TETRAHEDRON LETTERS,54(18),2271-2273.
MLA Hu, Yunbin,et al."A facile synthesis of 2,3,6,7-tetrabromonaphthalene diimides toward new pi-extended naphthalene diimides".TETRAHEDRON LETTERS 54.18(2013):2271-2273.

入库方式: OAI收割

来源:化学研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。