Copper(II) complexes of tetradentate N2S2 donor sets: Synthesis, crystal structure characterization and reactivity

被引:28
作者
Sarkar, S. [1 ]
Patra, A. [1 ]
Drew, M. G. B. [2 ]
Zangrando, E. [3 ]
Chattopadhyay, P. [1 ]
机构
[1] Univ Burdwan, Dept Chem, Burdwan 713104, W Bengal, India
[2] Univ Reading, Dept Chem, Reading RG 66AD, Berks, England
[3] Univ Trieste, Dipartimento Sci Chim, I-34127 Trieste, Italy
基金
英国工程与自然科学研究理事会;
关键词
Copper(II) complex; Copper(I) complex; Nitrogen-sulphur ligands; Crystal structure; NSNO PYRIDYLTHIOAZOPHENOL LIGANDS; OXORHENIUM(V) COMPLEXES; COORDINATION; NICKEL(II); DNA; QUADRIDENTATE; ACTIVATION; LIGHT; MODEL; SITE;
D O I
10.1016/j.poly.2008.08.004
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two mononuclear and one dinuclear copper(II) complexes, containing neutral tetradentate NSSN type ligands, of formulation [Cu-II(L-1)Cl]ClO4 (1), [Cu-II(L-2)Cl]ClO4 (2) and [Cu-2(II)(L-3)(2)Cl-2](ClO4)(2) (3) were synthesized and isolated in pure form [where L-1 = 1,2-bis(2-pyridylmethylthio)ethane, L-2 = 1,3-bis(2-pyridylmethylthio)propane and L-3 = 1,4-bis(2-pyridylmethylthio)butane]. All these green colored copper(II) complexes were characterized by physicochemical and spectroscopic methods. The dinuclear copper(II) complex 3 changed to a colorless dinuclear copper(I) species of formula [Cu-2(1)(L-3)(2)](ClO4)(2),0.5H(2)O (4) in dimethylformamide even in the presence of air at ambient temperature, while complexes I and 2 showed no change under similar conditions. The solid-state structures of complexes 1, 2 and 4 were established by X-ray crystallography. The geometry about the copper in complexes 1 and 2 is trigonal bipyramidal whereas the coordination environment about the copper(I) in dinuclear complex 4 is distorted tetrahedral. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
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