Artigo Revisado por pares

Pentamethyldisilylmethyl derivatives of the transition metals, LMCH2SiMe2SiMe3 [LM = (η5-C5R5)M(CO)nn−, M = Fe, W, R = H, Me, n = 2, 3; (η5-C9H7)Fe(CO)2−; (η5-C5 H5)2MCl−, M = Ti, Zr, Hf]

1991; Elsevier BV; Volume: 10; Issue: 11 Linguagem: Inglês

10.1016/s0277-5387(00)86094-5

ISSN

1873-3719

Autores

Sneh Sharma, Ramesh N. Kapoor, Francisco Cervantes‐Lee, Keith H. Pannell,

Tópico(s)

Organoboron and organosilicon chemistry

Resumo

Pentamethyldisilylmethyl derivatives of the transition metals have been synthesized, LMCH2SiMe2SiMe3 [LM = (η5-C5R5) M(CO)n−, M = Fe, W, R = H, Me, n = 2, 3; (η5-C9H7)Fe(CO)2−; (η5-C5H5) 2MCl−, M = Ti,Zr,Hf]. The cyclopentadienylcarbonyl complexes are photochemically labile with respect to rearrangement to LM-SiMe2 CH2SiMe3 and are also subject to base-induced migration to the cyclopentadienyl ring to form (η5-Me3SiCH2SiMe2C5H4) derivatives. The titanium, zirconium and hafnium complexes exhibit neither property; the only compound isolated from the photochemical treatment of these complexes being Me3SiSiMe3. Structural analyses of (η5-C5H5)W(CO)3 CH2SiMe2SiMe3 and its phosphine-substituted rearrangement product, (η5-C5H5)W(CO)2 (PPh3)SiMe2CH2SiMe3, are presented.

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