Direct electrochemical synthesis of copper(II) and zinc(II) complexes of the tetradentate ligand N,N′-bis(2-pyridinecarboxamide)-2-aminobenzylamine (H2bpabza). The crystal structures of the ligand and its Cu(II) complex

被引:6
作者
Meghdadi, Soraia [1 ]
Mirkhani, Valiollah [1 ]
Kia, Reza [2 ]
Moghadam, Majid [1 ]
Tangestaninejad, Sharam [1 ]
Mohammadpoor-Baltork, Iraj [1 ]
机构
[1] Univ Isfahan, Dept Chem, Esfahan 8174673441, Iran
[2] Sharif Univ Technol, Dept Chem, Tehran, Iran
关键词
Tetradentate unsymmetrical carboxamide; Electrochemical synthesis; Cu(II); Zn(II); complexes; X-ray structure; Polymeric Cu(II) complex; IONIC LIQUIDS; COBALT(III) COMPLEXES; CARBOXAMIDE LIGANDS; RUTHENIUM NITROSYLS; AMIDE; COORDINATION; DERIVATIVES; NICKEL(II); CONSTRUCTION; REACTIVITY;
D O I
10.1016/j.poly.2014.08.065
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The direct electrosynthesis of neutral copper(II) and zinc(II) complexes of a new unsymmetrical carboxamide ligand, N,N'-bis(2-pyridinecarboxamide)-2-aminobenzylamine (H(2)bpabza) derived from 2-pyridinecarboxylic acid and 2-aminobenzylamine, was accomplished by electrochemical oxidation of anodic metals (copper and zinc) in an acetonitrile solution of the ligand. These compounds were characterized by elemental analyses and different spectroscopic methods. The crystal and molecular structures of the ligand, H(2)bpabza, and its copper complex, Cu(bpabza), were determined by X-ray diffraction. The copper atom adopts a distorted square-pyramidal (4 + 1) CuN2N'N '' O coordination geometry with bpabza(2-) acting as a dianionic tetradentate ligand furnishing four N atoms in the base, with the O atom of a carbonyl group from an adjacent molecule in the apical position of the coordination environment. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:519 / 524
页数:6
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