7314-08-1Relevant articles and documents
Remote Substituent Effects on Methyl Torsional Barriers: trans-p-Amino-p'-methylstilbene
Yan, Shuxin,Spangler, Lee H.
, p. 3047 - 3052 (1995)
The expansion-cooled fluorescence excitation spectrum of trans-p-amino-p'-methylstilbene is presented.It displays several prominent low-frequency modes, including a progression in the methyl torsion.Fits of the torsional progression yield an S1 barrier of
Substituent effects on the 13C NMR chemical shifts of the imine carbon in N-(4-X-benzylidene)-4-(4-Y-styryl) anilines
Fang, Zhengjun,Cao, Chenzhong,Chen, Guanfan
, p. 1343 - 1350 (2013/08/24)
Long-range electronic substituent effects were targeted using the substituent dependence of δC(C=N), and specific cross-interactions were explored extendedly. A wide set of N-(4-X-benzylidene)- 4-(4-Y-styryl) anilines, p-X-C6H4
Spectroscopic characterization by laser flash photolysis of electrophilic intermediates derived from 4-aminostilbenes. Stilbene "nitrenium" ions and quinone methide imines
Bose, Rohit,Ahmad, Abid R.,Dicks, Andrew P.,Novak, Michael,Kayser, Kelly J.,McClelland, Robert A.
, p. 1591 - 1599 (2007/10/03)
This paper reports the observation in water-acetonitrile solutions of two electrophiles derived from 4-amino- and 4-acetylaminostilbene carcinogens - the 'nitrenium' ion ArCH=CHC6H4-N+R and the quinone methide imine ArCHOH
