Large hydroazaacene diimides: synthesis, tautomerism, halochromism, and redox-switchable NIR optics
Large hydroazaacene diimides: synthesis, tautomerism, halochromism, and redox-switchable NIR optics
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大型氢氮杂苯二酰亚胺:合成、互变异构、卤色现象和氧化还原可切换的近红外光学器件
DOI:
10.1039/c2sc21142d
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发表时间:
2012-11-01
期刊:
影响因子:
8.4
通讯作者:
Zhao, Dahui
中科院分区:
文献类型:
--
作者:
Cai, Kang;Yan, Qifan;Zhao, Dahui
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.