
Journal of Organometallic Chemistry p. 357 - 366 (1986)
Update date:2022-07-29
Topics:
Filippou, Alexander Constantin
Fischer, Ernst Otto
Alt, Helmut Guido
The reaction of trans-X(CO)4WCNR2 (X = Br, R = chex (cyclohexyl); X = Cl, R = chex, ipr (isopropyl)) with M+X- (M+ = NEt4+, X- = Br-; M+ = PPN+, X- = Cl-) leads under substitution of one CO ligand to new anionic dihalo(tricarbonyl)carbyne-tungsten complexes of the type M+ mer-<(X)2(CO)3WCNR2>- (M+ = NEt4+, X = Br, R = chex; M+ = PPN+, X = Cl, R = chex, ipr), whose composition and structure were determined by elemental analysis as well as by IR, 1H and 13C NMR spectroscopy.In the anionic carbyne complexes the entered halogen ligand, coordinated in a cis position relative to the carbyne ligand on the metal, can be easily substituted by neutral nucleophiles, as the reaction of PPN+ mer-<(Cl)2(CO)3WCNchex2>- with PPh3 demonstrates yielding the neutral carbyne complex mer-
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