Diastereoselective formation of metallamacrocyclic (arene)RuII and Cp*RhIII complexes

被引:60
作者
Lehaire, ML
Scopelliti, R
Herdeis, L
Polborn, K
Mayer, P
Severin, K [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Chim Mol & Biol, CH-1015 Lausanne, Switzerland
[2] Univ Munich, Dept Chem, D-81377 Munich, Germany
关键词
D O I
10.1021/ic035328i
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The reaction of [(arene)RuCl2](2) (arene = cymene, 1,3,5-C6H3Me3) and [Cp*RhCl2](2) half-sandwich complexes with tridentate heterocyclic ligands in the presence of base has been investigated. In all cases, the chloro-ligands were substituted to give metallacyclic products with ring sizes between 4 and 18 atoms. The cyclization occurs in a highly diastereoselective fashion with chiral recognition between the different metal fragments. The complexes were comprehensively characterized by elemental analysis, NMR spectroscopy, and single crystal X-ray crystallography. For 2-hydroxy-nicotinic acid and 2-amino-nicotinic acid, dinuclear structures were obtained (1517) whereas for 2,3-dihydroxyquinoline, 2,3-dihydroxyquinoxaline, and 6-methyl-2,3-phenazinediol, trimeric assemblies were found (19-22), and for 4-imidazolecarboxylic acid, a tetrameric assembly (18) was found.
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页码:1609 / 1617
页数:9
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