Synthesis and crystal structures of thermally stable titanocenes

被引:41
|
作者
Lukesová, L
Horácek, M
Stepnicka, P
Fejfarová, K
Gyepes, R
Císarová, I
Kubista, J
Mach, K
机构
[1] Acad Sci Czech Republ, J Heyrovsky Inst Phys Chem, CR-18223 Prague 8, Czech Republic
[2] Charles Univ Prague, Dept Inorgan Chem, CR-12840 Prague 2, Czech Republic
关键词
titanium; titanocenes; bent titanocenes; silyl substituents; X-ray crystallography;
D O I
10.1016/S0022-328X(02)01726-6
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Reduction of fully substituted titanocene dichlorides [TiCl2(eta(5)-C5Me4R)(2)] (R = SiMe2CH2CH2Ph, 3; SiMe2Ph, 4; and SiMePh2, 5) with magnesium in THF proceeds via the formation of titanocene monochlorides [TiCl(eta(5)-C5Me4R)(2)] 6-8 to afford monomeric titanocenes, [Ti(eta(5)-C5Me4R)(2)], 9-11. Titanocene monochlorides give the expected EPR spectra in toluene solution and glass. The structure of 7 was further corroborated by single-crystal X-ray diffraction. Titanocenes 9-11 are EPR silent down to -196 degreesC but exhibit paramagnetic broadening of the signals in solution NMR spectra. The positions of the NMR signals are temperature-dependent, obeying the Curie Law in the range investigated (0-60 degreesC). As revealed by X-ray crystallography, titanocenes 9 and 11 possess bent metallocene structures with the cyclopentadienyl rings tilted at an angle of 9.8(l) and 14.4(2)degrees, respectively. Titanocenes 9-11 are easily oxidized with PbCl2 to the parent dichloride complexes 3-5. Titanocenes 9 and 10 react with bis(trimethylsilyl)ethyne (btmse) only in large excess of the alkyne to give an equilibrium concentration of the respective [Ti(eta(5)-C5Me4R)(2)(eta(2)-Me3SiC drop CSiMe3)] complexes. On the other hand, titanocene 11 does not observably react with btmse. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
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页码:134 / 144
页数:11
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