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On the mechanisms of the reaction of dodecatungstophosphate with alkyl radicals in aqueous solutions
Authors:Inna Popivker  Israel Zilbermann  Eric Maimon  Yosef Matana  Dan Meyerstein
Affiliation:a Chemistry Department, Ben-Gurion University of the Negev, P.O. Box 653, Beer-Sheva 84105, Israel
b Chemistry Department, Nuclear Research Centre-Negev, P.O. Box 9001, Beer-Sheva 84105, Israel
c Biological Chemistry Department, Ariel University Center of Samaria, Ariel, Israel
Abstract:The reduced lacunary polyoxotungstate, [PW11O39]8−, reacts with the .CH2CH(OH)CH3 and .CH2C(CH3)2OH radicals via a mechanism involving β-hydroxide elimination to yield propene and 2-methyl propene respectively, and [PW11O39]7−. [PW11O39]8− is also oxidized by methyl radicals in a reaction which yields methane as the major product. It is proposed that the reactions proceed via the formation of short lived transients with W-C σ bonds.
Keywords:Polyoxotungstate   Alkyl radicals   Reaction mechanisms
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