Synthesis, spectral, electrochemical and catalytic properties of Cu(II), Ni(II) and Co(II) complexes containing N, O donors

被引:23
|
作者
Raja, K. Kanmani [3 ]
Easwaramoorthy, D. [3 ]
Rani, S. Kutti [3 ]
Rajesh, J. [1 ]
Jorapur, Y. [4 ]
Thambidurai, S. [5 ]
Athappan, P. R. [1 ]
Rajagopal, G. [2 ]
机构
[1] Madurai Kamaraj Univ, Dept Inorgan Chem, Madurai 625021, Tamil Nadu, India
[2] Govt Arts Coll Men Autonomous, Dept Chem, Madras 600035, Tamil Nadu, India
[3] BSA Crescent Engn Coll, Dept Chem, Vandalur 600048, India
[4] Nara Natl Coll Technol, Dept Chem Engn, Nara 6391080, Japan
[5] Periyar Arts Coll, Dept Chem, Cuddalore 607001, India
关键词
Schiff bases; Copper and nickel complexes; Cyanosilylation; Aldehydes; Electrochemical studies; SCHIFF-BASE LIGANDS; SOLVENT-FREE CYANOSILYLATION; ONE-POT SYNTHESIS; TRIMETHYLSILYL CYANIDE; CRYSTAL-STRUCTURES; METAL-COMPLEXES; ENANTIOSELECTIVE ADDITION; COPPER(II) COMPLEXES; CARBONYL-COMPOUNDS; REDOX PROPERTIES;
D O I
10.1016/j.molcata.2008.12.021
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Metal(II) chelates of Schiff bases derived from the condensation Of multi-substituted aniline with mono- and di-substituted salicylaldehyde have been prepared and characterized by H-1 NMR, IR, electronic, EPR, magnetic and cyclic voltammetry measurements. The complexes are of the type M(X-DPMP)(2) [(M = Cu(II), Ni(II) or Co(II)), DPMP = 2-[(2,6-diisopropylphenylimino)methyl]phenol, X = Br, Cl, I, BrCl]. The Schiff bases behave as monobasic bidentate ligand in their complexes. The spectral data indicate that the ligand coordinates through the phenolic oxygen and the azomethine nitrogen atoms. The observed A(II) values in the Cu(II) complexes indicate a tetrahedrally distorted square planar structure. The cyclic voltammetric redox potential of copper(II) and nickel(II) complexes suggest the existence of irreversible pairs in acetonitrile. Cu(Br-DPMP)(2) was found to be an efficient catalyst for cyanosilylation of aldehydes under mild conditions. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:52 / 59
页数:8
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