Issue 9, 1981

Flash photolysis study of phenyl-substituted phenols, quinones, and corresponding free radicals. Part 3. Intermediates in the photolysis of phenyl-substituted phenols

Abstract

Aryloxyl radicals are formed on photoexcitation of phenyl-substituted phenols in a biphotonic process involving the triplet excited state. These aryloxyl radicals are also formed on photolysis of the corresponding phenolate ions in the presence of oxygen involving the singlet excited state.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1981, 1237-1239

Flash photolysis study of phenyl-substituted phenols, quinones, and corresponding free radicals. Part 3. Intermediates in the photolysis of phenyl-substituted phenols

Petr. P. Levin, I. V. Khudyakov, V. A. Kuz'min, H. J. Hageman and C. R. H. I. de Jonge, J. Chem. Soc., Perkin Trans. 2, 1981, 1237 DOI: 10.1039/P29810001237

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