Dinoi C.Prikhodchenko P.Demirhan F.Gun J.Lev O.Daran J.-C.Poli R.2024-07-222024-07-2220070022328Xhttp://akademikarsiv.cbu.edu.tr:4000/handle/123456789/19277Reaction of Cp2*Mo2O5 with HSCH2CH2COOH in acidic (by CF3COOH) 50:50 MeOH-H2O solvent at room temperature yields compound Cp2*Mo2(μ-O)(μ-SCH2CH2CO2)2, a dinuclear diamagnetic MoIV compound with a two-leg-sharing bis(four-legged piano stool) structure and a Mo-Mo distance of 2.6833(6) Å. A reaction monitoring by ESI MS shows the formation of an intermediate 18 mass units heavier, interpreted as a dihydroxo analogue. Electrochemistry shows a reversible, pH independent oxidation process and an irreversible, pH-dependent reduction process. Contrary to a recently published analogous reaction with the closely related HSCH2COOH substrate, this process does not lead to C-S bond cleavage. © 2007 Elsevier B.V. All rights reserved.EnglishAll Open Access; Green Open AccessElectrochemistryInorganic acidsLigandsOrganometallicspH effectsReductionSolutionsAlkylsulfido ligandsAqueous organometallic chemistryCarboxylato ligandsMercaptopropionic acidPentamethylcyclopentadienyl ligandsMolybdenum compoundsShort survey10.1016/j.jorganchem.2007.02.046