The analysis of the IR, 13C NMR data along with the ab-initio calculations of some α-diethoxyphosphoryl- and α-ethylsulfonyl-carbonyl compounds indicated that the most stable gauche rotamer for both series is stabilized by charge transfer.
Comparative conformational and electronic interaction studies of some alpha-diethoxy-phosphoryl-carbonyl compounds and their alpha-ethylsulfonyl analogues
DISTEFANO, Giuseppe;DAL COLLE, Maurizio
1999
Abstract
The analysis of the IR, 13C NMR data along with the ab-initio calculations of some α-diethoxyphosphoryl- and α-ethylsulfonyl-carbonyl compounds indicated that the most stable gauche rotamer for both series is stabilized by charge transfer.File in questo prodotto:
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