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Turkish Journal of Chemistry, vol.23, no.1, pp.9-14, 1999 (SCI-Expanded)
Tetracarbonylbis(diphenylphosphino)alkanemetal(0) complexes of the general formula M(CO)4[(C6 H5)2P (CH2)n P(C6H5)2] (M: Cr, Mo, W; n: 1, 2, 3) were synthesized from the reaction of M(CO)4(η2:2 -1,5-cyclooctadiene) with the appropriate ligand and characterized by means of IR and NMR (13 C and 31P) spectroscopy. Spectroscopic data shows that two phosphorus atoms in the complexes are identical and occupy two cis-coordiantion sites in a pseudo-octahedral coordination sphere of the metal. The comparative study of the coordination shift and the 31P-13C coupling constant reveals that two carbonyl groups trans to one of two phosphorus atoms in the diphosphine ligand are shifted toward the lower magnetic field more than those which are cis to both phosphorus atoms. This is ascribed to the fact that two multiface ligands such as carbonyl or phosphine compete for the use of metal dπ-orbitals more strongly when they are trans to each other.