Half-Sandwich Rare-Earth-Metal Alkylaluminate Complexes Bearing Peripheral Boryl Ligands

被引:28
|
作者
Dettenrieder, Nicole [1 ]
Hollfelder, Christoph O. [1 ]
Jende, Lars N. [1 ]
Maichle-Mossmer, Cacilia [1 ]
Anwander, Reiner [1 ]
机构
[1] Univ Tubingen, Inst Anorgan Chem, D-72076 Tubingen, Germany
关键词
H BOND ACTIVATION; RAY CRYSTAL-STRUCTURE; ORGANOLANTHANIDE CHEMISTRY; POLYMERIZATION; REACTIVITY; ISOPRENE; YTTRIUM; ALKYL; TRIMETHYLALUMINUM; DERIVATIZATION;
D O I
10.1021/om401163a
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
[(C5Me5)LnMe(2)](3) (Ln = Y, Lu) dissolve readily in a n-hexane/toluene mixture upon addition of 3 equiv of the organoaluminum boryl compound [Me2Al{B(NDippCH)(2)}](2) (Dipp = C(6)H(3)iPr(2)-2,6). The half-sandwich complexes (C5Me5)Ln[(AlMe3){B(NDippCH)(2)}](2) thus formed display unsymmetrical heteroaluminate coordination not only in the solid state but also at lower temperatures in solution, which is distinct from the behavior of the homoaluminate congeners (C5Me5)Ln(AlMe4)(2). The effect of homo- versus heteroaluminate coordination is assessed in the coordinative polymerization of isoprene.
引用
收藏
页码:1528 / 1531
页数:4
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