Origin of the N-methyl and N-phenyl substituent effects on the fluorescence vibronic structures of trans-4-aminostilbene and its derivatives in hexane

Please use this identifier to cite or link to this item: http://ir.lib.ncu.edu.tw/handle/987654321/34550

Title:	Origin of the N-methyl and N-phenyl substituent effects on the fluorescence vibronic structures of trans-4-aminostilbene and its derivatives in hexane
Authors:	Yang,JS;Wang,CM;Hwang,CY;Liau,KL;Chiou,SY
Contributors:	化學研究所
Keywords:	CHARGE-TRANSFER STATE;EXCITED-STATE;MOLECULAR-STRUCTURE;PHOTOISOMERIZATION;SPECTROSCOPY;STILBENES;SPECTRA;BOND;4-(N;N-DIMETHYLAMINO)BENZONITRILE;DELOCALIZATION
Date:	2003
Issue Date:	2010-07-07 12:07:13 (UTC+8)
Publisher:	中央大學
Abstract:	The origin of the N- substituent effect on the room temperature fluorescence vibronic structures of trans- 4- aminostilbene ( 1), its disubstituted derivatives ( 2 and 3), and the fused- ring analogs ( 4) in hexane has been investigated. The fluorescence
Relation:	PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES
Appears in Collections:	[Graduate Institute of Chemistry] journal & Dissertation

Files in This Item:

File	Description	Size	Format
index.html		0Kb	HTML	489	View/Open

社群 sharing