Zirconium complexes of the tridentate bis(aryloxide)-N-heterocyclic-carbene ligand:: Chloride and alkyl functionalized derivatives

被引:55
作者
Zhang, Dao [1 ]
Aihara, Hidenori [1 ]
Watanabe, Takahito [1 ]
Matsuo, Tsukasa [1 ]
Kawaguchi, Hiroyuki [1 ]
机构
[1] Inst Mol Sci, Coordinat Chem Labs, Okazaki, Aichi 4448787, Japan
关键词
zirconium; carbene; aryloxide; multidentate ligand; HETEROCYCLIC CARBENE COMPLEXES; TRANSITION-METALS; CRYSTAL-STRUCTURE; OLEFIN METATHESIS; TITANIUM; COORDINATION; REACTIVITY; ACTIVATION; STABILITY; CHEMISTRY;
D O I
10.1016/j.jorganchem.2006.03.044
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The disodium salt of a bis(aryloxide)-N-heterocyclic-carbene dianionic ligand, Na-2[L], was prepared by reaction of 1,3-bis(4,6-di-tert-butyl-2-hydroxybenzyl)imidazolium bromide [H3L]Br with 3 equiv. of NaN(SiMe3)(2). Reaction of ZrCl4(thf)(2) with I equiv. of Na-2[L] gave a mixture of [L]ZrCl2(thf) (1) and [L](2)Zr (2). When the amount of Na-2[L] was increased to 2 equiv., the bis(bis(aryloxide)-N-heterocyclic-carbene) complex 2 was obtained in good yield. The dichloro complex I is a precursor to organometallic derivatives, and treatment with PhCH2MgCl or Me3SiCH2Li yielded [L]ZrR2 [R = CH2Ph (3), CH2SiMe3 (4)]. The disodium salt of the ligand Na2[L] is unstable and undergoes 1,2-benzyl migration, whereas zirconium complexes of the [L](2-) ligand are found to be thermally stable in solid and solution. The X-ray crystal structures of 1, 2, and 3 are described. (c) 2006 Elsevier B.V. All rights reserved.
引用
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页码:234 / 242
页数:9
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