On the mechanisms of the reaction of dodecatungstophosphate with alkyl radicals in aqueous solutions

Inna Popivker; Israel Zilbermann; Eric Maimon; Yosef Matana; Haim Cohen; Dan Meyerstein

doi:10.1016/j.ica.2010.06.046

On the mechanisms of the reaction of dodecatungstophosphate with alkyl radicals in aqueous solutions

Inna Popivker, Israel Zilbermann, Eric Maimon, Yosef Matana, Haim Cohen, Dan Meyerstein

Department of Chemical Sciences

Research output: Contribution to journal › Article › peer-review

3 Scopus citations

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-. [PW ₁₁O₃₉]^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.

Original language	English
Pages (from-to)	4202-4206
Number of pages	5
Journal	Inorganica Chimica Acta
Volume	363
Issue number	15
DOIs	https://doi.org/10.1016/j.ica.2010.06.046
State	Published - 10 Dec 2010

Keywords

Alkyl radicals
Polyoxotungstate
Reaction mechanisms

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10.1016/j.ica.2010.06.046

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title = "On the mechanisms of the reaction of dodecatungstophosphate with alkyl radicals in aqueous solutions",

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-. [PW 11O39]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 = "Alkyl radicals, Polyoxotungstate, Reaction mechanisms",

author = "Inna Popivker and Israel Zilbermann and Eric Maimon and Yosef Matana and Haim Cohen and Dan Meyerstein",

note = "Funding Information: This study was supported in part by a grant from the Budgeting and Planning Committee of The Council of Higher Education and the Israel Atomic Energy Commission.",

year = "2010",

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doi = "10.1016/j.ica.2010.06.046",

language = "אנגלית",

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journal = "Inorganica Chimica Acta",

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T1 - On the mechanisms of the reaction of dodecatungstophosphate with alkyl radicals in aqueous solutions

AU - Popivker, Inna

AU - Zilbermann, Israel

AU - Maimon, Eric

AU - Matana, Yosef

AU - Cohen, Haim

AU - Meyerstein, Dan

N1 - Funding Information: This study was supported in part by a grant from the Budgeting and Planning Committee of The Council of Higher Education and the Israel Atomic Energy Commission.

PY - 2010/12/10

Y1 - 2010/12/10

N2 - 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-. [PW 11O39]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.

AB - 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-. [PW 11O39]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.

KW - Alkyl radicals

KW - Polyoxotungstate

KW - Reaction mechanisms

UR - https://www.scopus.com/pages/publications/78649453726

U2 - 10.1016/j.ica.2010.06.046

DO - 10.1016/j.ica.2010.06.046

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AN - SCOPUS:78649453726

SN - 0020-1693

VL - 363

SP - 4202

EP - 4206

JO - Inorganica Chimica Acta

JF - Inorganica Chimica Acta

IS - 15

ER -

On the mechanisms of the reaction of dodecatungstophosphate with alkyl radicals in aqueous solutions

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