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Résonance Magnétique Nucléaire de 17O. Aldéhydes et cétones aliphatiques: additivité des effets de substitution et corrélation avec la 13C-RMN
Authors:Claude Delseth  Jean-Pierre Kintzinger
Abstract:17O-NMR. Aliphatic aldehydes and ketones, additivity of substituent effects and correlation with 13C-NMR. The 17O-chemical shifts of 9 aldehydes, 22 aliphatic and 4 alicyclic ketones, in the natural abundance FT.-NMR. spectra followed a good correlation with the 13C-chemical shifts of the terminal C-atoms of corresponding methylene compounds. An additivity relation involving 6 parameters represents the 17O-shifts of 28 of the measured products with a standard deviation of 2.5 ppm. The additivity parameters are discussed with respect to the modifications of the polarity of the carbonyl group induced by the hyperconjugative interaction of π and π* orbitals with the πCH 3 orbitals of the alkyl substituent groups.
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