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Chemistry ; 12(4): 1266-73, 2006 Jan 23.
Artigo em Inglês | MEDLINE | ID: mdl-16281318

RESUMO

Reaction of [(eta5-C5H4Li)(eta7-C7H6Li)Cr]tmeda with a variety of dialkyl(dichloro)silanes in aliphatic solvents afforded the corresponding [1]silatrochrocenophanes. Structural characterization by X-ray diffraction analysis of the [1]silatrochrocenophanes bearing Me2Si, (iPr)2Si, and silacyclobutane bridges revealed tilt angles alpha of 15.56(12) degrees , 15.8(1) degrees , and 16.33(17) degrees , respectively. Analogously, a [2]silatrochrocenophane (6) was prepared in excellent yield by reaction of [(eta5-C5H4Li)(eta7-C7H6Li)Cr]tmeda with 1,2-dichloro-1,1,2,2-tetramethyldisilane. This complex also was characterized structurally and exhibited a tilt angle alpha of 2.60(15) degrees. The [1]silatrochrocenophane bearing the Me2Si bridge underwent facile and regioselective carbon-silicon bond cleavage with [Pt(PEt3)4] to give a very high yield of an oxidative addition product. The ring-opening polymerization of these novel [1]silatrochrocenophanes afforded ring-opened chromium-based polymers.

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