Neutral and cationic trimethylsilylmethyl complexes of the rare earth metals supported by a crown ether: synthesis and structural characterization

被引:40
作者
Arndt, S
Zeimentz, PM
Spaniol, TP
Okuda, J
Honda, M
Tatsumi, K
机构
[1] Johannes Gutenberg Univ Mainz, Inst Anorgan Chem & Analyt Chem, D-55099 Mainz, Germany
[2] Nagoya Univ, Dept Chem, Chikusa Ku, Nagoya, Aichi 4648602, Japan
关键词
D O I
10.1039/b305964b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis of a series of thermally robust, isolable trimethylsilylmethyl complexes of the rare earth metals stabilized by 12-crown-4 [Ln(CH2SiMe3)(3)(12-crown-4)] (Ln = Sc, Y, Sm, Gd, Tb, Dy, Ho, Er, Tm, Yb, Lu) is reported. The crystallographically characterized yttrium and lutetium complexes [Ln(CH2SiMe3)(3)(12-crown-4)] exhibit facial coordination of the crown ether at the neutral lanthanide trialkyl unit. The coordination geometry can be derived from a capped octahedron. VT NMR spectroscopic studies revealed a labile coordination of the crown ether in thf solution. Reaction of the diamagnetic derivatives with triethylammonium tetraphenylborate in thf results in the clean formation of the cationic dialkyl complexes [Ln(CH2SiMe3)(2)(12-crown-4)(thf)(y)][BPh4] (Ln = Sc, Y, y = 0; Ln = Lu, y = 1), which also exhibit an exocyclic coordination of the crown ether to the cationic dialkyl lanthanide fragment.
引用
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页码:3622 / 3627
页数:6
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