Bifunctional pincer-type organometallics as substrates for organic transformations and as novel building blocks for polymetallic materials

被引:103
作者
Rodríguez, G
Albrecht, M
Schoenmaker, J
Ford, A
Lutz, M
Spek, AL
van Koten, G
机构
[1] Univ Utrecht, Debye Inst, Dept Met Mediated Synth, NL-3584 CH Utrecht, Netherlands
[2] Univ Utrecht, Bijvoet Ctr Biomol Res, Dept Crystal & Struct Chem, NL-3584 CH Utrecht, Netherlands
关键词
D O I
10.1021/ja0177657
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The reactivity of the bifunctionalized ligand NC(Br)N\ 1 [IC6H2(CH2NMe2)(2)-3,5-Br-4] has been studied as a versatile synthon for organic and/or organometallic synthesis. Chemoselective metalation (M = Pd, Pt, LI) at the C-aryl-1 or C-aryl-Br bonds was achieved by choosing the appropriate metal precursors. In this way a series of Pt-II and Pd-II complexes were prepared that have a second functional group available for further reactions. These Pt-II and Pd-II complexes were subjected to a wide range of organic and organometallic reactions, revealing the remarkable stability of their M-C sigma-bond and opening an easy route for the synthesis of mono- and (hetero)bimetallic building blocks. The scope of the chemistry of such building blocks shows that they are good candidates for use in the synthesis of dendrimers, bioorganometallic systems, or polymetallic materials. The X-ray crystal structures of the most representative complexes (2, 3a, 19, 20, and 24) are also reported.
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收藏
页码:5127 / 5138
页数:12
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