Issue 0, 1968
From the journal:

Journal of the Chemical Society C: Organic

Reactions of the free toluene-p-sulphonyl radical. Part I. Diagnostic reactions of free radicals

C. M. M. da Silva Corrêa  and  William A. Waters  

Abstract

The free p·CH3·C6H4·SO2 radical is easily produced by the thermolysis or photolysis of p·Me·C6H4·SO2·l; copper powder assists the removal of iodine and so do radicals R2C(CN)·. Evidence is presented to show that p·Me·C6H4·SO2·l adds homolytically to olefins and that free p·Me·C6H4·SO2· radicals tend to disproportionate according to the equation: 6 Me·C6H4·SO2·→ 2(Me·C6H4·SO2)2O + Me·C6H4·S·SO2·C6H4·Me p·Me·C6H4·SO2· radicals add to the oxygen atoms of quinones giving the ditoluene-p-sulphonate esters of quinols. Arylsulphinyl radicals do not appear to have a similar reactivity; they merely dimerise to thiolsulphonate esters Ar·S·SO2·Ar.

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Article information

DOI
https://doi.org/10.1039/J39680001874
Article type
Paper

J. Chem. Soc. C, 1968, 1874-1879

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Reactions of the free toluene-p-sulphonyl radical. Part I. Diagnostic reactions of free radicals

C. M. M. da Silva Corrêa and W. A. Waters, J. Chem. Soc. C, 1968, 1874 DOI: 10.1039/J39680001874

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