Chromium, molybdenum and tungsten carbonyl derivatives of distibinomethane ligands[hair space]

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Angela M. Hill, Nicholas J. Holmes, Anthony R. J. Genge, William Levason, Michael Webster and Synke Rutschow


Abstract

Substituted Group 6 carbonyl complexes of the distibinomethane ligands Ph2SbCH2SbPh2 (dpsm) and Me2SbCH2SbMe2 (dmsm) of types [M(CO)51-dpsm)] (M = Cr, Mo or W), [(OC)5M(µ-dpsm)M(CO)5] (M ≠ Mo), [(OC)5M(µ-dmsm)M(CO)5], [(OC)4M(µ-dpsm)2M(CO)4], [(OC)4M(µ-dmsm)2M(CO)4] and fac-[M(CO)31-dpsm)3] have been isolated and characterised by chemical analysis, IR, NMR (1H, 13C-{1H}, 95Mo) spectroscopy and FAB mass spectrometry. The crystal structures of [W(CO)5(dpsm)], [{W(CO)5}2(dpsm)], [{W(CO)4(dpsm)}2] and [{W(CO)4(dmsm)}2] have been determined. Complexes of η1-dmsm have been observed but are too unstable to isolate in a pure state. Both the ligands function as monodentate or bridging bidentates in the complexes characterised, but no examples with chelated distibinomethanes have been prepared. Comparisons are drawn with complexes of related diphosphine ligands.


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