Synthesis and Electrochemistry of M(II) N2O2 Schiff Base Complexes: X-Ray Structure of {Ni[Bis(3-chloroacetylacetone)ethylenediimine]}

被引:9
作者
Kianfar, A. H. [1 ]
Zargari, S. [2 ]
Khavasi, H. R. [3 ]
机构
[1] Univ Yasuj, Dept Chem, Yasuj, Iran
[2] Kurdistan Univ, Dept Chem, Sanandaj, Iran
[3] Shahid Beheshti Univ, Dept Chem, GC, Tehran, Iran
关键词
Cobalt(II); Nickel(II); Cu(II); Schiff base complexes; Electrochemistry; SOLVENT-EXCHANGE-REACTIONS; OXYGENATION CATALYSTS; COPPER(II) COMPLEXES; NICKEL(II) COMPLEXES; ELECTRON-TRANSFER; CRYSTAL-STRUCTURE; 1ST EVIDENCE; LIGANDS; REDUCTION; SPECTROSCOPY;
D O I
10.1007/BF03246087
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The synthesis and characterization of [Ni(BCE)] and [Cu(BCE)] (where BCE = bis(3-chloroacetylacetone)ethylenediimine) are described. The coordination geometry of [Ni(BCE)] was determined by X-ray crystallography. It was found to be planar and four coordinate in the solid state. The electrochemical properties of M(Chel), where M = Co(II), Ni(II) and Cu(II), and Chel = BAE (bis(acetylacetone) ethylenediimine), BBE = bis(benzoylacetone) ethylenediimine, BFE (bis(1,1,1-triflouroacetylacetone) ethylenediimine and BCE ligands were investigated in DMF and DMSO as solvents. The oxidation potentials changed from left to right in the periodic table in the trend: Co < Ni < Cu, while the reduction potentials changed according to the trend: Ni > Co > Cu. The oxidation potentials of M(II) to M(III) (M = Ni and Cu) increased according to the Schiff base ligands in the trend: BAE < BBE < BCE < BFE, while the reduction potentials followed a reverse trend: BAE > BBE > BCE > BFE. The oxidation potentials of M(II) to M(III) increased according to the solvent in the trend: DMSO < DMF.
引用
收藏
页码:908 / 916
页数:9
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