Aqueous reduction of [Cp*2W2O5]: Characterization of the triangular clusters [Cp*3W 3O4(OH)2]2+ and [Cp* 3W3O6]+ - Comparison with molybdenum

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dc.contributor.authorDinoi C.
dc.contributor.authorSözen P.
dc.contributor.authorTaban G.
dc.contributor.authorDemir D.
dc.contributor.authorDemirhan F.
dc.contributor.authorPrikhodchenko P.
dc.contributor.authorGun J.
dc.contributor.authorLev O.
dc.contributor.authorDaran J.-C.
dc.contributor.authorPoli R.
dc.date.accessioned2025-04-10T11:16:51Z
dc.date.available2025-04-10T11:16:51Z
dc.date.issued2007
dc.description.abstractZinc reduction of Cp*2W2O5 in an acidified water-methanol medium affords the green 3-electron trinuclear cluster [Cp*3W3O4(OH)2]2+, isolated and crystallographically characterized as the triflate salt, 1. Upon exposure to air, this complex is oxidized to a related 2-electron cluster, [Cp*3W3O6]+, which was crystallized and characterized in three different salts, 2-4. The 3-electron cluster exhibits a near-tetragonal frozen-glass EPR spectrum, and it shows evidence of coupling of the unpaired electron to only one of the three W atoms. The two-electron cluster is diamagnetic. An electrospray ionization MS n study revealed a stepwise expulsion of neutral [Cp*WO 2] units as the main fragmentation process. DFT calculations unveiled the intimate details of the electronic structures of these complexes and fully rationalized the structural and spectroscopic properties. © Wiley-VCH Verlag GmbH & Co. KGaA, 2007.
dc.identifier.DOI-ID10.1002/ejic.200700419
dc.identifier.urihttp://hdl.handle.net/20.500.14701/52149
dc.publisherWiley-VCH Verlag
dc.titleAqueous reduction of [Cp*2W2O5]: Characterization of the triangular clusters [Cp*3W 3O4(OH)2]2+ and [Cp* 3W3O6]+ - Comparison with molybdenum
dc.typeArticle

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