| Literature DB >> 15998041 |
Jie Zhang1, Alan M Bond, Douglas R MacFarlane, Stewart A Forsyth, Jennifer M Pringle, Andrew W A Mariotti, Abigail F Glowinski, Anthony G Wedd.
Abstract
The electrochemical reduction of tetrabutylammonium salts of isostructural pairs of polyoxometalates [Bu4N]2[M6O19], [Bu4N]4[alpha-SiM12O40], and [Bu4N]4[alpha-S2M18O62] (M = Mo or W) has been investigated at glassy carbon electrodes in dissolved and surface-confined states in ionic liquids and other media. In the ionic liquid 1-n-butyl-3-methylimidazolium hexafluorophosphate [BMIM][PF(6)], between two and six reversible one-electron-transfer processes were detected. Detailed studies on the process [alpha-S2W18O62](4-/5-) in a range of ionic liquids, water, and conventional organic solvents (containing 0.1 M electrolyte) suggest that the polarity of the medium plays a key role in the determination of the reversible potential. Reduction processes involving very highly charged [alpha-S2W18O62](8-/9-/10-) species are strongly influenced by the purity of the medium.Entities:
Year: 2005 PMID: 15998041 DOI: 10.1021/ic050032t
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165