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.
1999
Olivato, Pr; Ruiz, R; ZUKERMAN SCHPECTOR, J; Distefano, Giuseppe; DAL COLLE, Maurizio
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11392/1201073
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