Large hydroazaacene diimides: synthesis, tautomerism, halochromism, and redox-switchable NIR optics

被引：59

作者：

Cai, Kang

Yan, Qifan

Zhao, Dahui ^{[1
]}

机构：

[1] Peking Univ, Dept Appl Chem, Beijing Natl Lab Mol Sci, Coll Chem, Beijing 100871, Peoples R China

来源：

CHEMICAL SCIENCE | 2012年 / 3卷 / 11期

基金：

中国国家自然科学基金;

关键词：

THIN-FILM TRANSISTORS; NAPHTHALENE-DIIMIDE; EFFICIENT SYNTHESIS; MORPHOLOGY CONTROL; AMBIPOLAR; NITROGEN; ACENES; SEMICONDUCTORS; PERFORMANCE; DERIVATIVES;

D O I：

10.1039/c2sc21142d

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A series of dihydro- and tetrahydro-tetraazaacene diimides containing 6 or 7 laterally fused six-membered rings were synthesized. Halochromic and redox-switchable vis-NIR optical characteristics were exhibited. Quinonoid tautomers of dihydrotetraazaacene derivatives were obtained and characterized, which exhibited adequate stability and existed in equilibrium with the more commonly observed benzenoid tautomer.

引用

收藏

页码：3175 / 3182

页数：8

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