Ring expansion of a Cp moiety upon CO insertion: Synthesis and characterization of [(η6-C6H5OCo)Co3(CO)9]

被引:5
|
作者
Bose, Shubhankar Kumar [1 ]
Geetharani, K. [1 ]
Ghosh, Sundargopal [1 ]
机构
[1] Indian Inst Technol, Dept Chem, Madras 600036, Tamil Nadu, India
关键词
Vanadaborane; Co-2(CO)(8); Ring expansion; CO insertion; TETRAHEDRAL CLUSTER CO-4(CO)(12); CARBON BOND ACTIVATION; CO-59; NMR; CRYSTAL-STRUCTURE; CYCLOPENTADIENYL LIGAND; MIXED-METAL; MCO3; M; COMPLEXES; CLEAVAGE; COBALT;
D O I
10.1016/j.jorganchem.2010.08.004
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Reaction of [(CpV)(2)(B2H6)(2)], 1 (Cp - eta(5)-C5H5) with four equivalents of [Co-2(CO)(8)] or [Co-4(CO)(12)] in hexane at 70 degrees C leads to the isolation of the tetranuclear carbonyl cluster, [(eta(6)-C6H5OCo)Co-3(CO)(9)], 2 in modest yield. The geometry of 2 is similar to that of [Co-4(CO)(12)] where all the four Co atoms are arranged in a tetrahedral geometry. The apical cobalt atom in 2 is coordinated to C6H5O ring in a eta(6)-fashion and the other three cobalt atoms are each coordinated to three carbonyl ligands. Compound 2 has been characterized in solution by IR, H-1, C-13 NMR and mass spectrometry and the structural types were unequivocally established by crystallographic analysis. (C) 2010 Elsevier B. V. All rights reserved.
引用
收藏
页码:2567 / 2571
页数:5
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