Nitroxide radicals. Part 20. Formation and reactions of t-butyl p-formylphenyl nitroxide and its derivatives
Alexander R. Forrester, John W. Henderson, S. P. Hepburn
Abstract
Alexander R. Forrester, John W. Henderson, S. P. Hepburn
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.
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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.
Key concepts: Nitroxide mediated radical polymerization, Hydroxylamine, Chemistry, Radical, Aryl, Combinatorial chemistry, Photochemistry, Organic chemistry