Studies of electrode kinetics of mixed ligand complexes of Ni(II) in tetrahydrofuran (THF) at DME

被引:0
|
作者
Jain, S [1 ]
Sharma, A [1 ]
Pandey, R [1 ]
Sharma, IK [1 ]
机构
[1] Univ Rajasthan, Dept Chem, Jaipur 302004, Rajasthan, India
来源
BULLETIN OF ELECTROCHEMISTRY | 2003年 / 19卷 / 01期
关键词
reduction; dropping mercury electrode (d.m.e); tetrahydrofuran (THF); kinetic parameters;
D O I
暂无
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The reduction of synthesized mixed ligand complexes of Ni(II) with pyridines and halides and pseudohalides have been studied at dropping mercury electrode in different percentages (v/v) of tetrahydrofuran (THF). The reduction of each of these complexes, i.e. Ni(beta-PiC)(4) (NCS)(2), Ni(gamma-PiC)(4) (NCS)(2), Ni(PY)(4) (NCS)(2), Ni(beta-PiC)(4) Cl-2, Ni(gamma-Pic)(4) Cl-2, Ni(PY)(4) Cl-2 was found to be diffusion controlled. The slope values indicate the reduction to be irreversible. This was further confirmed by the plot of E-1/2 vs log t, which indicates a change of E-1/2 with drop. time or height of mercury column. The kinetic parameters (K-fh(0) cm and xi) of these complexes have been calculated by using Meites-Israel method and its modifications by Gaur-Bhargava's method. The results of the kinetic parameters suggest that with the increase in percentages of the solvent (upto 60%) the reduction takes place irreversibly. Moreover, the reduction of the aquo-nickel ion takes place more irreversibly than that of nickel complexes.
引用
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页码:27 / 30
页数:4
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