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RESEARCH PRODUCT

Synthesis of μ-C2S44− Cobalt Complexes by Activation of the 1,3,4,6-tetrathiapentalene-2,5-dione, and Electrochemical Study of [(Cp*Co)2(μ-C2S4)]

Theresa MonzonIsabelle JourdainFabrice GuyonNarcis AvarvariMichael KnorrYves MugnierDominique LucasMarc Fourmigué

subject

ChemistryStereochemistrychemistry.chemical_elementCrystal structureElectrochemistryOxidative additionMedicinal chemistryInorganic ChemistryMetalvisual_artYield (chemistry)visual_art.visual_art_mediumMoleculeCobaltBimetallic strip

description

The bimetallic complex [Cp(*)Co)2(μ-C2S4)] in which the two metal centres are linked by an ethylenetetrathiolate C2S44− unit, was synthesized in high yield by oxidative addition of 1,3,4,6 tetrathiapentalene-2,5-dione to [Cp(*)Co(CO)2]. The X-ray crystal structure of the intermediate product Cp*Co(dmid) (dmid2− = 4,5-disulfanyl-1,3-dithiol-2-onate) is presented. The electrochemical behaviour of the [(Cp*Co)2(μ-C2S4)] complex was studied in detail in the oxidative range. This study has shown that the nature of the product obtained after oxidation depends on the presence of complexing agent in the solution. The mechanism has been elucidated in a CH2Cl2 solution in the presence of P(OMe)3. In addition, chemical oxidation was conducted with several oxidizing agents (Br2, TCNQF4, and AgBF4). The molecular structure of the tetrathiooxalate bridged complex [(Cp*Co{P(OMe)3})2(μ-C2S4)](BF4)2 was established by an X-ray diffraction study. (© Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002)

https://doi.org/10.1002/1099-0682(200208)2002:8<2026::aid-ejic2026>3.0.co;2-0