Interaction of half-sandwich alkylmolybdenum(III) complexes with B(C6F5)3.: The X-ray structure of [CpMo(η4-C4H6)(μ-Cl)(μ-CH2)(O)MoCp][CH3B(C6F5)3]

被引:1
作者
Le Grognec, E
Poli, R
Richard, P
Llusar, R
Uriel, S
机构
[1] Univ Bourgogne, Fac Sci Gabriel, Lab Synthese & Electrosynthese Organometall, F-21000 Dijon, France
[2] Univ Jaume 1, Dept Ciencies Expt, Castellon de La Plana 12080, Spain
关键词
half-sandwich; X-ray structure; EPR properties; molybdenum; butadiene ligand;
D O I
10.1016/S0022-328X(01)01196-2
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reactions of the half-sandwich molybdenum(III) complexes CpMo(eta (4)-C4H4R2)(CH3)(2), where Cp=eta (5)-C5H5 and R=H or CH3, with equimolar amounts of B(C6F5)(3) have been investigated in toluene. EPR monitoring shows the formation of an addition product which does not readily react with Lewis bases such as ethylene, pyridine, or PMe3. The analysis of the EPR properties and the X-ray structure of a decomposition product obtained from dichloromethane, [CPMo(eta (4)-C4H6)(mu -Cl)(mu- CH2)(O)MoCp][CH3B(C6F5)(3)], indicate that the borane attack has occurred at the methyl position. (C) 2001 Elsevier Science BN. All rights reserved.
引用
收藏
页码:113 / 120
页数:8
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