Comparative structural coordination chemistry of two tricyclic bisamidines

被引:7
作者
Li, Jingwei [1 ]
Widlicka, Daniel W. [1 ]
Fichter, Kerry [1 ]
Reed, David P. [1 ]
Weisman, Gary R. [1 ]
Wong, Edward H. [1 ]
DiPasquale, Antonio [2 ]
Heroux, Katie J. [2 ]
Golen, James A. [3 ]
Rheingold, Arnold L. [2 ]
机构
[1] Univ New Hampshire, Dept Chem, Durham, NH 03824 USA
[2] Univ Calif San Diego, Dept Chem & Biochem, La Jolla, CA 92093 USA
[3] Univ Massachusetts Dartmouth, Dept Chem & Biochem, N Dartmouth, MA 02747 USA
关键词
Tricyclic bisamidine; Metal complexes; Crystal structures; METAL-COMPLEXES; LIGANDS; CRYSTAL; CATALYSIS;
D O I
10.1016/j.ica.2010.08.015
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The tricyclic bisamidines L1 and L2 are designed to be preconstrained so as to present synperiplanar donor sites for metal coordination. Their very different bite angles of 35 degrees and 70 degrees result from the incorporation of two five-membered instead of six-membered rings in their respective backbones. Distinct coordination preferences in a variety of metal complexes have now been confirmed by X-ray structural studies. While L1 afforded monodentate, symmetrical and unsymmetrical chelating as well as bimetallic bridging modes in its complexes, L2 has been found exclusively in a bidentate chelating mode. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:185 / 194
页数:10
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