Abstract

The compounds [W(CR)(CO)2(η-C5H5)](R = C6H4Me-4 or Me) and [[graphic omitted]H2}(η-C5H5)2] react in toluene, in the presence of tetrahydrofuran, to afford the bridged vinyl complexes [TiW{µ-C(R)CH2}(µ-CO)(CO)(η-C5H5)3]. The compound with R = C6H4Me-4 may also be prepared by treating [TiW(µ-CC6H4Me-4)(µ-CO)(CO)(µ-C5H5)3] with the titanium reagent. It has been structurally characterised by X-ray diffraction. The Ti–W bond [3.082(2)A] is spanned by a σ:η2-CO ligand [W–C–O 173.4(3)°, Ti–C 2.222(4), Ti–O– 2.285(3)A] and by a σ:η2-C(C6H4Me)CH2 group, σ bonded to titanium and η2 co-ordinated to tungsten [Ti–C 2.290(4), CC 1.441(6), W–C 2.199(5) and 2.268(6)A]. The tungsten atom carries a terminally bound CO ligand and a C5H5 group, and the titanium atom is ligated by two C5H5 groups. Reactions between the dimetal compounds [PtW(µ-CR)(CO)2(PMe3)2(η-C5H5)] and [[graphic omitted]H2}(η-C5H5)2] afford the complexes [PtW{µ-C(R)CH2}(CO)2(PMe3)2(η-C5H5)]. An X-ray diffraction study on the platinum–tungsten species with R = C6H4Me-4 established the structure as one in which the Pt–W bond [2.820(1)A] is bridged by a C(C6H4Me-4)CH2 group, as in the titanium–tungsten compound, being σ bonded to the platinum and η2 co-ordinated to the tungsten. The metal–metal bond is semi-bridged by one CO ligand [W–C–O 166(1)°], while the remaining CO is terminally bound to tungsten, which also carries the C5H5 group. The platinum is ligated by two PMe3 ligands, and is in a distorted square-planar environment defined by the two phosphorus atoms, and the µ-C atoms of the semi-bridging carbonyl and the vinyl group. Spectroscopic properties of the new dimetal compounds are reported, and their mechanisms of formation discussed in the light of 1H and 13C-{1H} n.m.r. studies on reaction mixtures.

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