Syntheses, structures, and dynamic properties of M(CO)2(η3-C3H5)(en)(X) (M = Mo, W; X = Br, N3, CN) and [(en)(η3-C3H5)(CO)2M(μ-CN)M(CO)2 (η3-C3H5)(en)]Br (M = Mo, W)

被引:11
|
作者
Liu, Fu-Chen [1 ]
Tsai, Tu-Chieh [1 ]
Lin, Yu-Liang [1 ]
Lee, Chen-Shiang [1 ]
Yang, Pei-Shan [1 ]
Wang, Ju-Chun [2 ]
机构
[1] Natl Dong Hwa Univ, Dept Chem, Hualien 974, Taiwan
[2] Soochow Univ, Dept Chem, Taipei 11102, Taiwan
关键词
Ethylenediamine; Allylic; Cyanide; Fluxional; MOLYBDENUM-CATALYZED ALKYLATIONS; DICARBONYL-ALLYL DERIVATIVES; CYANO-BRIDGED COMPLEXES; SUBSTITUTED CARBONYLS; MOLECULAR-STRUCTURE; TUNGSTEN COMPLEXES; CRYSTAL-STRUCTURE; ALPHA-DIIMINES; REACTIVITY; LIGANDS;
D O I
10.1016/j.jorganchem.2009.10.031
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Mononuclear compounds M(CO)(2)(eta(3)-C3H5)(en)(X) (X = Br, M = Mo(1), W(2); X = N-3, M = Mo(3), W(4); X = CN, M = Mo(5), W(6)) and cyanide-bridged bimetallic compounds [(en)(eta(3)-C3H5)(CO)(2)M(mu-CN)M(CO)(2)(eta(3)-C3H5)(en)]Br (M = Mo (7), W(8)) were prepared and characterized. These compounds are fluxional and display broad unresolved proton NMR signals at room temperature. Compounds 1-6 were characterized by NMR spectroscopy at -60 degrees C, which revealed isomers in solution. The major isomers of 1-4 adopt an asymmetric endo-conformation, while those of 5 and 6 were both found to possess a symmetric endo-conformation. The single crystal X-ray structures of 1-6 are consistent with the structures of the major isomer in solution at low temperature. In contrast to mononuclear terminal cyanide compounds 5 and 6, cyanide-bridged compounds 7 and 8 were found to adopt the asymmetric endo-conformation in the solid state. (C) 2009 Elsevier B.V. All rights reserved.
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页码:423 / 430
页数:8
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