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Synthesis, structure and spectroscopic characterization of sodium tetrabutylammonium tris(thiobenzilato)-molybdate(IV)

AutorCervilla, Antonio; Gómez-Romero, P.
Fecha de publicación1992
EditorAmerican Chemical Society
CitaciónJournal of the Chemical Society, Dalton Transactions (6): 1005-1008 (1992)
ResumenThe synthesis, structure and spectroscopic properties of the mixed salt [NBun4]Na[Mo{O2CC(S)Ph2}3]·H2O·MeOH are reported. It crystallizes in the space group Pbca, with a= 19.369(6), b= 25.175(6), c= 24.273(6)Å, and Z= 8. The molybdenum atom is six-co-ordinated and bonded to both the thiolate sulfur and carboxylate oxygen atoms of each of the three co-ordinated thiobenzilate ligands. The average Mo–S and Mo–O distances are 2.291(4) and 2.076(9)Å, respectively, the former being the shortest observed for any tris(chelate)molybdenum complex. Contrary to the result predicted from previous molecular orbital calculations, the co-ordination polyhedron around the molybdenum atom is essentially trigonal prismatic. The two triangular faces, formed by three sulfur and three oxygen atoms from the thiolate and carboxylate groups, respectively, are nearly parallel and twisted by ca. 4.7° with respect to a regular prism. Sodium cations are intercalated between Mo(S3O3) units and are also subject to a trigonal-prismatic co-ordination by three carboxylate oxygen atoms, two water and one methanol molecule. Cyclic voltammetry indicates that [Mo{O2CC(S)Ph2}3]2– undergoes a reversible one-electron oxidation to [Mo{O2CC(S)Ph2}3]– at –0.26 V (ESR parameters 〈g〉= 1.968, 〈A〉= 36 × 10–4 cm–1). The latter species can also be generated in solution by chemical oxidation.
Identificadoresdoi: 10.1039/DT9920001005
issn: 1472-7773
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