1981Journal of the Chemical Society Perkin Transactions 1Requires access

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

Open publisher page 10 citations

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.

About this research paper

What this paper is about

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.

Why it matters

OpenAlex reports 10 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available 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.

Key concepts: Nitroxide mediated radical polymerization, Hydroxylamine, Chemistry, Radical, Aryl, Combinatorial chemistry, Photochemistry, Organic chemistry

Related papers

Back to paper searchBrowse research topicsOriginal source
Nitroxide radicals. Part 20. Formation and reactions of t-butyl p-formylphenyl nitroxide and its derivatives — Research Paper | ScholarLens