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Aqueous Phase One-Electron Reduction of Sulfonium, Selenonium and Telluronium Salts
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Kemiska institutionen. Institutionen för biokemi och organisk kemi, Organisk kemi I. Organisk kemi.
2005 (engelsk)Inngår i: Eur. J. Org. Chem., s. 701-705Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Triorganylsulfonium, -selenonium and -telluronium salts were reduced by carbon dioxide radical anions/solvated electrons produced in aqueous solution by radiolysis. The radical expulsion accompanying reduction occurred with the expected leaving group propensities (benzyl > secondary alkyl> primary alkyl> methy> phenyl), although greater than expected loss of the phenyl group was often observed. Diorganyl chalcogenides formed in the reductions were conveniently isolated by extraction with an organic solvent. Product yields based on the amount of reducing radicals obtained from the y-source were often higher than stoichiometric (up to 1800%) in the reduction of selenonium an dtelluronium compounds; it is likely that this result can be accounted for in terms of a chain reaction with carbon-centred radicals/formate serving as the chain transfer agent. The product distribution was essentially independent of the reducing species for diphenyl alkyl telluronium salts, whereas significant variations were seen for some of the corresponding selenonium salts. This would suggest the intermediacy of telluranyl radicals in the one-electron reduction of telluronium salts. However, pulse radiolysis experiments indicated that the lifetimes of such a species (the triphenyltelluranyl radical) would have to be less than 1 us.

sted, utgiver, år, opplag, sider
2005. s. 701-705
Emneord [en]
Radicals, One-electron reduction, Sulfonium salts, Selenonium salts, Telluronium salts
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Identifikatorer
URN: urn:nbn:se:uu:diva-69996DOI: doi:10.1002/ejoc.200400604OAI: oai:DiVA.org:uu-69996DiVA, id: diva2:97907
Tilgjengelig fra: 2005-04-13 Laget: 2005-04-13 Sist oppdatert: 2011-01-12

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