Electronic interaction between the methyl group and trigonal carbon
JB Lambert, RJ Nienhuis
Index: Lambert, Joseph B.; Nienhuis, Ronald J. Journal of the American Chemical Society, 1980 , vol. 102, # 22 p. 6659 - 6665
Full Text: HTML
Citation Number: 8
Abstract
Abstract: The nature of the interaction between methyl and a trigonal carbon has been examined by the effect of substituents on the methyl rotational barrier. Barriers have been measured for para-substituted toluenes and for cis-and trans-substituted propenes by the motional effects of methyl rotation on dipole-dipole spin-lattice relaxation. The toluene barriers exhibit a fair correlation with u1 and a very poor one with uR. Thus ...
Related Articles:
Formartion of unsaturated sulfides by pyrolytical elimination
[Prochazka,M.; Durdovic,P. Collection of Czechoslovak Chemical Communications, 1977 , vol. 42, p. 2401 - 2407]
Prototropic isomerisation of unsaturated sulfides, sulfoxides and sulfones
[Svata,V. et al. Collection of Czechoslovak Chemical Communications, 1978 , vol. 43, p. 2619 - 2634]
Prototropic isomerisation of unsaturated sulfides, sulfoxides and sulfones
[Svata,V. et al. Collection of Czechoslovak Chemical Communications, 1978 , vol. 43, p. 2619 - 2634]
Isomerization processes in the synthesis of asymmetric allyl chalcogenides
[Deryagina; Korchevin Russian Chemical Bulletin, 1996 , vol. 45, # 1 p. 223 - 225]