
Journal of Organometallic Chemistry p. 321 - 332 (1989)
Update date:2022-08-10
Topics:
Tainturier, Gerard
Fahim, Mohammed
Trouve-Bellan, Gwenaaelle
Gautheron, Bernard
Dissymmetrical four-membered bimetallocenacycles (t-BuC5H4)2M(μ-S)2M'-(RC5H4)2 (M, M' = Zr, Hf; R = H, t-Bu) have been prepared and found to give redistribution products in solution at 190 deg C; identification of these products shows that the reaction involves exclusive cleavage of a metal-sulfur bond.Elemental sulfur and selenium react with chalcogen-containing complexes.The reaction is shown to involve the introduction of chalcogenic species in place of the ?-ligands of the complex to give either four-membered bimetallic complexes or catenated pentachalcogen metallocenic compounds.Some examples of insertion of sulfur and tellurium into the zirconium-methyl bond are also described.
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