Source:http://linkedlifedata.com/resource/pubmed/id/17928919
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
40
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pubmed:dateCreated |
2007-10-11
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pubmed:abstractText |
The electrochemistry of the Dawson-like sulfite polyoxometalate anion alpha-[Mo18O54(SO3)2]6-, derived from the TEAH6{alpha-[Mo18O54(SO3)2]} salt (TEAH+ is the triethanolammonium cation; pKa=7.8), has been investigated in aqueous media using cyclic and rotated disk voltammetry at glassy carbon electrodes and bulk electrolysis, with a focus on the pH-dependence for oxidation to alpha-[Mo18O54(SO3)2]4-. In buffered media at pH>or=4, the cyclic voltammetric response for alpha-[Mo18O54(SO3)2]6- reveals two partially resolved one-electron oxidation processes corresponding to the sequential generation of alpha-[Mo18O54(SO3)2]5- and alpha-[Mo18O54(SO3)2]4-. At lower pH, using electrolytes containing sulfuric acid, the two waves coalesce but the individual apparent E0' reversible formal potential values for the two processes can be extracted down to pH 2 by assuming that reversible protonation accompanies fast electron transfer. The results for 2<or=pH<or=8 are well described by the double-square scheme mechanism: [FORMULAS: SEE TEXT] where A, B and C correspond to species alpha-[Mo18O54(SO3)2]4-, alpha-[Mo18O54(SO3)2]5- and alpha-[Mo18O54(SO3)2]6- respectively. The following thermodynamic values could be deduced: E=-0.009 V vs. Fc+/Fc; E=-0.125 V vs. Fc+/Fc and KC=1.5x10(-5) M; values for KA, KB, E and E could not be determined. Protonated alpha-[HMo18O54(SO3)2]5-, deduced to be the major species present at pH<4, is highly stable in aqueous media. In contrast, alpha-[Mo18O54(SO3)2]6-, which is dominant at higher pH values, slowly decomposes. Data considered in the context of acid-base properties of both the TEAH+ cation and alpha-[HMo18O54(SO3)2]5- anion imply that the TEAH+ cation is important in the isolation of (TEAH)6{alpha-[Mo18O54(SO3)2]}. Cyclic and rotating disk electrode voltammetries demonstrate that at least 8 electrons also can be easily added to the [Mo18O54(SO3)2]4- framework in acidic media. The existence of the electron transfer series alpha-[Mo18O54(SO3)2]4-/5-/6-/7-/8- was confirmed by cyclic voltammetric studies of water insoluble [Pn4N]4{alpha-[Mo18O54(SO3)2]} adhered to a glassy carbon electrode in contact with an aqueous 0.1 M Et4NCl electrolyte.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Anions,
http://linkedlifedata.com/resource/pubmed/chemical/Ethanolamines,
http://linkedlifedata.com/resource/pubmed/chemical/Molybdenum,
http://linkedlifedata.com/resource/pubmed/chemical/Sulfites,
http://linkedlifedata.com/resource/pubmed/chemical/Tungsten Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/polyoxometalate I,
http://linkedlifedata.com/resource/pubmed/chemical/triethanolamine
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1477-9226
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
28
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
4599-607
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pubmed:meshHeading |
pubmed-meshheading:17928919-Anions,
pubmed-meshheading:17928919-Electrochemistry,
pubmed-meshheading:17928919-Electrons,
pubmed-meshheading:17928919-Ethanolamines,
pubmed-meshheading:17928919-Hydrogen-Ion Concentration,
pubmed-meshheading:17928919-Molybdenum,
pubmed-meshheading:17928919-Oxidation-Reduction,
pubmed-meshheading:17928919-Sulfites,
pubmed-meshheading:17928919-Tungsten Compounds
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pubmed:year |
2007
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pubmed:articleTitle |
pH-dependence of the aqueous electrochemistry of the two-electron reduced alpha-[Mo18O54(SO3)] sulfite Dawson-like polyoxometalate anion derived from its triethanolammonium salt.
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pubmed:affiliation |
School of Chemistry, Monash University, Clayton, Victoria 3800, Australia.
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pubmed:publicationType |
Journal Article
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