基于铜(II)、钴(II)、镍(II)和锌(II)离子配合物的新型3,4-二氯n-((5-氯吡啶-2-基)氨基甲氧基)苯酰胺的电化学研究

Ali A. A. Al-Riyahee, Diyar M. A. Murad, Ashwaq Shenta
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引用次数: 2

摘要

采用两步法合成了新型N,N′-二取代苯甲酰硫脲配体[3,4-二氯-N-(5-氯吡啶-2-基)氨基甲酰基)苄酰胺](L)。第一步用3,4-二氯苯甲酰氯在CH3CN溶剂中回流KSCN,第二步用第一步所得滤液与2-氨基-5-氯吡啶反应。将铜(II)、钴(II)、镍(II)和锌(II)氯化物和乙酸盐在DMF/H2O或CHCl3/甲醇的溶剂混合物中以1:1和1:2的摩尔比(M:L)与L配体配位,形成具有分子式{[LMCl2]和[L2M](CH3COO)2的配合物,M=铜(II)、钴(II)、镍(II)和锌(II)离子}。以1:1和1:2 (M:L)两种原料的摩尔比制备氯配合物,产物的分子式为[LMCl2],在相同条件下得到的醋酸盐配合物分子式为[L2M](CH3COO)2。用质谱、元素分析、磁矩、电导率、溶解度、紫外光谱、红外光谱、核磁共振光谱对配体L及其配合物[LCuCl2]、[LCoCl2]、[LNiCl2]、[LZnCl2]、[L2Cu](CH3COO)2、[L2Co](CH3COO)2、[L2Ni](CH3COO)2和[(L)2Zn](CH3COO)2进行了表征。采用循环伏安法(CV)进行了电化学研究。结果表明,铜(II)配合物具有准可逆的一次电子转移性质,而镍(II)和钴(II)配合物具有连续两次不可逆的电子转移性质。通过紫外光观察、元素分析、摩尔电导率、磁矩测量和溶解度测试表明,所制备的配合物中的金属离子均为四种配位方形平面结构,[LCuCl2]、[LCoCl2]、[LNiCl2]、[LZnCl2]为中性配合物,[L2Cu](CH3COO)2、[L2Co](CH3COO)2、[L2Ni](CH3COO)2和[(L)2Zn](CH3COO)2为阴离子配合物。观察到的磁矩显示锌(II)和镍(II)配合物具有抗磁性,而铜(II)和钴(II)则表现为顺磁性。FT-IR分析通过吡啶环上的氮原子和C=S基团上的硫原子两个位点确定了中心金属离子与配体L的配位。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Electrochemical Studies Of Novel 3,4-Dichloro-N-((5-ChloroPyridin-2-yl)Carbamothioyl)Benzamide Based On Its Complexes With Copper(II), Cobalt(II), Nickel(II) and Zinc(II) ions
The synthesis of novel N,Nʹ-disubstituted benzoyl thiourea ligand [3,4-dichloro-N-((5-chloropyridin-2-yl)carbamothioyl) benzamide] (L) is achieved in two steps. First step by refluxing KSCN with 3,4-dichloro benzoyl chloride in CH3CN solvent and the other step by the reaction of the resulting filtrate from the first step with 2-amino-5-chloropyridine. The copper(II), Cobalt(II), Nickel(II) and Zinc(II) chloride and acetate salts were coordinated with L ligand in the 1:1 and 1:2 mole ratios (M:L) in the solvent mixture of DMF/H2O or CHCl3/methanol to form the complexes with structural formulas {[LMCl2] and [L2M](CH3COO)2, M= Copper(II), Cobalt(II), Nickel(II) and Zinc(II) ions}. Two mole ratios of the starting materials, 1:1 and 1:2 (M:L) were experimented to form chloride complexes, the product was with structural formula [LMCl2] while acetate complexes with [L2M](CH3COO)2 formula are resulted with the same conditions. Ligand L and its complexes [LCuCl2], [LCoCl2], [LNiCl2], [LZnCl2], [L2Cu](CH3COO)2, [L2Co](CH3COO)2, [L2Ni](CH3COO)2 and [(L)2Zn](CH3COO)2 have been characterized by mass spectrometry, elemental analysis, magnetic moments, conductivity measurements, solubility test, UVvisible, FTIR, H and C NMR spectroscopies. Electrochemical studies were probed by using cyclic voltammetry technique(CV). The data reflect the quasi-reversible reductive nature for the Copper(II) complexes with one electron transfer process while Nickel(II) and Cobalt(II) complexes exhibited two consecutive irreversible reductive nature. The observed UVvisible, elemental analysis, molar conductivity, magnetic moment measurements and solubility test revealed that the metal ion in the all prepared complexes adopted four coordinated square planar structures and [LCuCl2], [LCoCl2], [LNiCl2], [LZnCl2], are formed as neutral complexes while [L2Cu](CH3COO)2, [L2Co](CH3COO)2, [L2Ni](CH3COO)2 and [(L)2Zn](CH3COO)2 adopted anion complexes. The observed magnetic moments show diamagnetic properties of Zinc(II) and Nickel(II) complexes while Copper(II) and Cobalt(II) appeared as paramagnetic species. FT-IR analysis confirmed the coordination sites between the central metal ion with ligand L through two sites, the nitrogen atom in pyridyl ring and the sulphur atom in C=S group.
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