Synthesis and crystal structure of new early-lanthanide organometallic clusters

被引:11
作者
Barnea, Eyal
Averbuj, Claudia
Kapon, Moshe
Botoshansky, Mark
Eisen, Moris S. [1 ]
机构
[1] Technion Israel Inst Technol, Schulich Fac Chem, IL-32000 Haifa, Israel
[2] Technion Israel Inst Technol, Inst Catalysis Sci & Technol, IL-32000 Haifa, Israel
关键词
organolanthanide halide clusters; lithium; bridging ligands;
D O I
10.1002/ejic.200601167
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Reaction of CP*2NdCl center dot LiCl.2thf (1) with excess catecholborane affords the hexameric cluster (Cp*NdCl2)(6)(LiCl)(3)(thf)(3) (2) bearing three types of bridging chloride ions. Heating the reaction mixture affords the tetrameric cluster [(Cp*NdCl2)(4)(mu(4)-Cl)](2)[LiO2][LiO2*Li2O*O-2] (3), which has the first crystal structure with the LiO2+ motif. Reaction of complex 1 or the analogous Sm complex, 4, with pinacolborane affords clusters 5a (Nd) or 5b (Sm), respectively, it second type of hexameric cluster built from two CpNd3Cl5(thf) units bonded by two mu(2)-Cl atoms. ((c) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2007).
引用
收藏
页码:4535 / 4540
页数:6
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