Issue 7, 1977

Long-range couplings in 2-alkoxycarbonylphenyl nitroxide radicals

Abstract

Solutions of 2-alkoxycarbonylphenylhydroxylamines in carbon tetrachloride contain long-lived 2-alkoxycarbonylphenyl nitroxide radicals which show long-range hyperfine splitting constants due to coupling with protons in the alkyl residue of the ester group, in their e.s.r. spectra. Selective line broadening in the 1H n.m.r. spectra of the hydroxylamines due to exchange with the radical is observed.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1977, 904-907

Long-range couplings in 2-alkoxycarbonylphenyl nitroxide radicals

B. G. Cox, R. J. Gillespie, R. S. Hay, A. E. A. Porter and J. S. Roberts, J. Chem. Soc., Perkin Trans. 2, 1977, 904 DOI: 10.1039/P29770000904

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