Spectrophotometric and conductometric study of complexation of salophen and some transition metal ions in nonaqueous polar solvents

被引:32
作者
Joshaghani, Mohammad [1 ]
Gholivand, Mohammad B. [1 ]
Ahmadi, Farhad [1 ]
机构
[1] Razi Univ, Fac Sci, Dept Chem, Kermanshah 67149, Iran
关键词
Schiff base complexation; salophen; thermodynamic parameters; nonaqueous solvents;
D O I
10.1016/j.saa.2007.10.015
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
The complexation reaction between Cu2+, Co2+ and Ni2+ metal cations with N.N'-bis(salicylidene)-1,2-phenylenediamine (salophen), in three nonaqueous polar solvents such as: acetonitrile (AN), dimethyl sulfoxide (DMSO), methanol (MeOH) and two binary mixtures of AN:DMSO and AN:MeOH at 25 degrees C were studied by spectrophotometric and conductometric methods. All investigated metal ions form 1:1 ML complex which their stability constants were determined and increase as Irving-Willianis stability order Co2+ < Ni2+ < Ni2+ < Cu2+ in all solvent systems except in the pure MeOH and binary mixture of AN:MeOH 20:80; in which, Ni2+ < Co2+ < Cu2+ was observed. The values of the thermodynamic parameters (Delta H degrees, Delta S degrees and Delta G degrees) for complexation reactions obtained from the temperature dependence of the stability constants and the results show that for all metal ion complexes, the value of Delta H degrees, Delta S degrees and Delta G degrees are solvent dependent. (C) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:1073 / 1078
页数:6
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