Issue 15, 1983

The preparation and X-ray crystal structures of 4-methyl-1,3,2-dithiazolium hexafluoroarsenate(V) and 5-methyl-1,3,2,4-dithiadiazolium hexafluoroarsenate(V) and their reduction to stable free radicals

Abstract

Acetonitrile, propyne, and acetylene react essentially quantitatively with S2NAsF6 to give the hexafluoroarsenate salts of 5-methyl-1,3,2,4-dithiadiazolium, 4-methyl-1,3,2-dithiazolium, and 1,3,2-dithiazolium respectively, the structures of the former two salts being determined by X-ray crystallography; the cations have been reduced chemically and electrolytically to form long-lived free redicals identified by their e.s.r. spectra.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 807-808

The preparation and X-ray crystal structures of 4-methyl-1,3,2-dithiazolium hexafluoroarsenate(V) and 5-methyl-1,3,2,4-dithiadiazolium hexafluoroarsenate(V) and their reduction to stable free radicals

G. K. MacLean, J. Passmore, M. J. Schriver, P. S. White, D. Bethell, R. S. Pilkington and L. H. Sutcliffe, J. Chem. Soc., Chem. Commun., 1983, 807 DOI: 10.1039/C39830000807

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