Title of article
A facile synthesis of 2,3,6,7-tetrabromonaphthalene diimides toward new π-extended naphthalene diimides
Author/Authors
Hu، نويسنده , , Yunbin and Wang، نويسنده , , Zhongli and Yang، نويسنده , , Xiaodi and Zhao، نويسنده , , Zheng and Han، نويسنده , , Wenjie and Yuan، نويسنده , , Wei and Li، نويسنده , , Hongxiang and Gao، نويسنده , , Xike and Zhu، نويسنده , , Daoben، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2013
Pages
3
From page
2271
To page
2273
Abstract
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 π-extended naphthalene diimide (1), which exhibits n-type behavior in organic transistors and interesting response to F− among halide anions in solutions.
Keywords
synthetic method , organic semiconductor , Naphthalene diimide , Anion–? interaction
Journal title
Tetrahedron Letters
Serial Year
2013
Journal title
Tetrahedron Letters
Record number
1884314
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