Hydro- and chloro-substituted silyl- and silyl-η1 -amido-η5- tetramethylcyclopentadienyl titanium complexes

Chlorosilyl-cyclopentadienyl titanium precursors [Ti(η5-C5Me4SiMeXCl)Cl3] (X=H 2, Cl 3) were prepared by reaction of TiCl4 with the trimethylsilyl derivatives of the corresponding cyclopentadienes. Methylation of these compounds with MgClMe under appropriate conditions afforded the methyl complexes...

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Detalles Bibliográficos
Autores: Vázquez García, Ana Belén, Royo Gracia, Pascual, Herdtweck, Eberhardt
Tipo de recurso: artículo
Fecha de publicación:2003
País:España
Institución:Universidad de Alcalá (UAH)
Repositorio:e_Buah Biblioteca Digital Universidad de Alcalá
Idioma:inglés
OAI Identifier:oai:ebuah.uah.es:10017/4187
Acceso en línea:http://hdl.handle.net/10017/4187
https://dx.doi.org/10.1016/S0022-328X(03)00559-X
Access Level:acceso abierto
Palabra clave:Titanium
Tetramethyl cyclopentadienyl
Linked amido-cyclopentadienyl
Chlorosilyl-cyclopentadienyl
Methyl complexes
Ciencia
Química inorgánica
Science
Chemistry, inorganic
Descripción
Sumario:Chlorosilyl-cyclopentadienyl titanium precursors [Ti(η5-C5Me4SiMeXCl)Cl3] (X=H 2, Cl 3) were prepared by reaction of TiCl4 with the trimethylsilyl derivatives of the corresponding cyclopentadienes. Methylation of these compounds with MgClMe under appropriate conditions afforded the methyl complexes [Ti(η5-C5Me4SiMe2R)XMe2] (R=H, X=Cl 5, Me 6; R=X=Me 7). Reactions of 2 and 3 with two equivalents of LiNHtBu afforded the ansa-silyl-η-amido compounds [Ti{η5-C5Me4SiMeX(η1-NtBu)}Cl2] (X=H 8, Cl 9). Methylation of 8 gave [Ti{η5-C5Me4SiMeH(η1-NtBu)}Me2] 10. Complex 9 was also obtained by reaction of 8 with BCl3, whereas the same reaction using alternative chlorinating agents (TiCl4, HCl) resulted in deamidation to give 2, which was also converted into 3 by reaction with BCl3. All of the new compounds were characterized by NMR spectroscopy and the molecular structures of 2 and 4 were determined by X-ray diffraction methods.