Issue 9, 1992

Iminoxy free radicals derived from diethyl (1-hydroxyimino)phosphonates. An EPR study

Abstract

Iminoxy radicals containing the diethyl phosphonate group have been synthesized and characterized by means of EPR spectroscopy. Structures of the Z and E isomers have been established on the basis of hyperfine splitting due to 14N, 31P, and 1H nuclei. The higher stability of the E isomer over the Z isomer has been established by analysis of anisotropic spectra. The source of a dependence of the 31P hyperfine constant on the solvent polarity is discussed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1992, 1421-1424

Iminoxy free radicals derived from diethyl (1-hydroxyimino)phosphonates. An EPR study

P. J. Chmielewski, A. Jezierski and Z. Siatecki, J. Chem. Soc., Perkin Trans. 2, 1992, 1421 DOI: 10.1039/P29920001421

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