16552-39-9Relevant articles and documents
Electronic and steric effects in the SNAr substitution reactions of substituted anilines with 2,4-dinitrophenyl 2,4,6-trinitrophenyl ether in acetonitrile
Crampton, Michael R.,Emokpae, Thomas A.,Isanbo, Chukwuemeka
, p. 75 - 80 (2007/10/03)
Rate measurements are reported for the reactions of 12 ring-substituted anilines with 2,4-dinitrophenyl 2,4,6-trinitrophenyl ether (1) in acetonitrile. Formation of the products, the correspondingly substituted 2,4,6- trinitrodiphenylamines, occurs without the observation of intermediates in detectable amounts by both base-catalysed and uncatalysed pathways and Hammett ρ value were determined for these processes. The results show that although substituents at the 3- or 4-positions of the anilines have only small steric effects, alkyl substituents at the 2-position may result in considerable reductions in reactivity. These effects are more pronounced for the base-catalysed pathway and in 2,6-dimethylaniline the uncatalysed pathway takes all the reaction flux. In the case of the 2-fluoro substituent the electronic effect, strong inductive electron withdrawal, is dominant over steric effects. Copyright
PHOTOELECTRON SPECTRA AND ELECTRONIC STRUCTURE OF para-SUBSTITUTED N-PICRYLANILINES
Redchenko, V. V.,Semenov, S. G.,Mikhalev, O. V.,Il'ina, I. G.
, p. 2315 - 2322 (2007/10/02)
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