PI-H3C5(ME2SI)(ME2SISIME2)-PI-C5H3 - A NOVEL AND SIMPLE DOUBLE-BRIDGED DICYCLOPENTADIENYL LIGAND - SYNTHESIS AND EXAMPLE OF ITS APPLICATIONIN THE CHEMISTRY OF COMPLEXES
P. Jutzi et al., PI-H3C5(ME2SI)(ME2SISIME2)-PI-C5H3 - A NOVEL AND SIMPLE DOUBLE-BRIDGED DICYCLOPENTADIENYL LIGAND - SYNTHESIS AND EXAMPLE OF ITS APPLICATIONIN THE CHEMISTRY OF COMPLEXES, Journal of organometallic chemistry, 541(1-2), 1997, pp. 9-17
Deprotonation of dicyclopentadienyldimethylsilane with two equivalents
of n-butyllithium and subsequent reaction with 1,2-dichlorotetramethy
ldisilane yields the double-bridged dicyclopentadiene H4C5(SiMe2)(Si2M
e4)C5H4 (1 = H2L). Reaction of 1 with two equivalents of n-butyllithiu
m leads to the dilithio compound Li-2 [H3C5(SiMe2)(Si2Me4)C5H3] (2 = L
i2L) with the bridging dimethylsilyl and tetramethyldisilanyl group in
1,2 position (ortho-position) at each cyclopentadienyl unit 2 is used
as starting material for the exemplary synthesis of the following met
al complexes: Cp '' Cl2ZrLZrCl2Cp '' (3; Cp '' = 1,3-(t-Bu)(2)C5H3), C
p '' Cl2ZrLH (4); Me5C5RuLRuC5Me5 (syn: 5a; anti: 5b); syn-(CO)(2)CoLC
o(CO)(2) (6). All compounds are characterized by spectroscopic and ana
lytical data. X-ray crystal structures are presented for 1 and for 3.
Stereochemical effects in metal complexes with the new unsymmetrically
bridged dicyclopentadienyl ligand L are discussed.