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

doi:10.1039/c2sc21142d

CORC > 北京大学 > 化学与分子工程学院

	Large hydroazaacene diimides: synthesis, tautomerism, halochromism, and redox-switchable NIR optics
	Cai, Kang ; Yan, Qifan ; Zhao, Dahui
刊名	chemical science
	2012
关键词	THIN-FILM TRANSISTORS FIELD-EFFECT TRANSISTORS NAPHTHALENE-DIIMIDE MORPHOLOGY CONTROL ORGANIC TRANSISTORS EFFICIENT SYNTHESIS CHARGE-TRANSPORT SEMICONDUCTORS AMBIPOLAR NITROGEN
DOI	10.1039/c2sc21142d
英文摘要	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.; http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000311068100007&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=8e1609b174ce4e31116a60747a720701 ; Chemistry, Multidisciplinary; SCI(E); EI; 23; ARTICLE; 11; 3175-3182; 3
语种	英语
内容类型	期刊论文
源URL	[http://ir.pku.edu.cn/handle/20.500.11897/392746]
专题	化学与分子工程学院
推荐引用方式 GB/T 7714	Cai, Kang,Yan, Qifan,Zhao, Dahui. Large hydroazaacene diimides: synthesis, tautomerism, halochromism, and redox-switchable NIR optics[J]. chemical science,2012.
APA	Cai, Kang,Yan, Qifan,&Zhao, Dahui.(2012).Large hydroazaacene diimides: synthesis, tautomerism, halochromism, and redox-switchable NIR optics.chemical science.
MLA	Cai, Kang,et al."Large hydroazaacene diimides: synthesis, tautomerism, halochromism, and redox-switchable NIR optics".chemical science (2012).