Journal of Organometallic Chemistry p. 137 - 148 (1983)
Update date:2022-08-05
Topics:
Budzelaar, P. H. M.
Alberts-Jansen, H. J.
Mollema, K.
Boersma, J.
Kerk, G. J. M. van der
The stabilities of simple and internally coordinated organozinc-transition metal compounds towards disproportionation have been investigated by the microwave titration technique.Simple alkyl- and aryl-derivatives disproportionate to such an extent as to preclude isolation.Internal coordination was found to stabilize the asymmetric compounds, and several derivatives containing the dimethylaminopropyl group were isolated.The crystal structure of one of them, Me2N(CH2)3ZnW(Cp)(CO)3, was determined by a single-crystal X-ray study.The crystals are orthorhombic, space group P212121, with four molecular units in a cell with parameters a 8.406(1), b 12.179(2) and c 16.642(2) Angstroem.The structure was solved by standard Patterson and Fourier techniques.The refinement, with anisotropic temperature factors for the two heavy atoms, converged at RF = 0.092 (RwF = 0.089) for 1536 observed reflections with I > 2.5?(I).The molecule consists of a central tungsten atom, surrounded in a tetragonal pyramidal fashion by a cyclopentadienyl group in the apical position and three carbon monoxyde molecules and a zinc atom occupying the basal positions.The zinc atom is three-coordinate, being surrounded by the tungsten atom and the chelating dimethylaminopropyl group: there is, however, a short intermolecular contact between zinc and a carbonyl oxygen atom at 2.61(3) Angstroem.
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