Issue 0, 1981

Nitroxide radicals. Part 20. Formation and reactions of t-butyl p-formylphenyl nitroxide and its derivatives

Abstract

Preparation of the parent hydroxylamine of the title nitroxide and its conversion into several hydroxylamine derivatives and the corresponding nitroxides has been achieved with a view to using functionalised aryl nitroxides as spin labels. The aN values of the derived aryl nitroxides vary with the nature of their para-substituents, thus providing a potential method for identifying the site of attachment of aryl nitroxide spin labels.

Reactions of a nitrone-nitroxide, derived from the title radical, with cyanoisopropyl, phenyl, benzoyloxyl, and t-butoxyl radicals were investigated. In no case was a bisnitroxide formed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1981, 1165-1172

Nitroxide radicals. Part 20. Formation and reactions of t-butyl p-formylphenyl nitroxide and its derivatives

A. R. Forrester, J. Henderson and S. P. Hepburn, J. Chem. Soc., Perkin Trans. 1, 1981, 1165 DOI: 10.1039/P19810001165

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