Issue 15, 1972

Electron spin resonance spectra of radicals derived from arylhydroquinones

Abstract

The e.s.r. spectra of radicals formed in the autoxidation of arylhydroquinones show hyperfine splitting from protons attached to the aryl group, showing that the odd electron is delocalised over both rings. Substituents on the phenyl group influence the various proton coupling constants in a way which is related to their electron-donating or electron-withdrawing properties.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1972, 2264-2267

Electron spin resonance spectra of radicals derived from arylhydroquinones

P. Ashworth and W. T. Dixon, J. Chem. Soc., Perkin Trans. 2, 1972, 2264 DOI: 10.1039/P29720002264

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