Issue 9, 1970

Nitroxide radicals. Part VIII. Stability of ortho-alkyl-substituted phenyl t-butyl nitroxides

Abstract

t-Butyl o-tolyl nitroxides disproportionate slowly, giving o-aminobenzaldehydes and hydroxylamines. t-Butyl 2,6-xylyl nitroxides, however, are exceptionally stable. Attempted isolation of the diradical, o-phenylene di-t-butyl-dinitroxide, was unsuccessful because of its rapid decomposition to an aminoquinone imine N-oxide.

Article information

Article type
Paper

J. Chem. Soc. C, 1970, 1277-1280

Nitroxide radicals. Part VIII. Stability of ortho-alkyl-substituted phenyl t-butyl nitroxides

A. R. Forrester and S. P. Hepburn, J. Chem. Soc. C, 1970, 1277 DOI: 10.1039/J39700001277

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements