Reduction of [Mo2O5] by mercaptopropionic acid in an aqueous medium. Isolation and characterization of a dinuclear oxo- and 3-sulfido-proprionato(2-)-bridged molybdenum(IV) compound
Autor: | Ovadia Lev, Jean-Claude Daran, Jenny Gun, Petr V. Prikhodchenko, Chiara Dinoi, Rinaldo Poli, Funda Demirhan |
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Rok vydání: | 2007 |
Předmět: |
Aqueous medium
010405 organic chemistry Electrospray ionization Organic Chemistry Inorganic chemistry chemistry.chemical_element Substrate (chemistry) 010402 general chemistry Electrochemistry 01 natural sciences Biochemistry Medicinal chemistry 0104 chemical sciences 3. Good health Inorganic Chemistry Solvent chemistry Molybdenum Materials Chemistry Physical and Theoretical Chemistry Mercaptopropionic acid Bond cleavage |
Zdroj: | Journal of Organometallic Chemistry. 692:2599-2605 |
ISSN: | 0022-328X |
DOI: | 10.1016/j.jorganchem.2007.02.046 |
Popis: | Reaction of Cp*2Mo2O5 with HSCH2CH2COOH in acidic (by CF3COOH) 50:50 MeOH-H2O solvent at room temperature yields compound Cp*2Mo2(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) A. 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. |
Databáze: | OpenAIRE |
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