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首页> 外文期刊>Journal of Molecular Structure >A new copper(II) Schiff base complex containing asymmetrical tetradentate N2O2 Schiff base ligand: Synthesis, characterization, crystal structure and DFT study
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A new copper(II) Schiff base complex containing asymmetrical tetradentate N2O2 Schiff base ligand: Synthesis, characterization, crystal structure and DFT study

机译:含不对称四齿N2O2 Schiff碱配体的新型席夫铜(II)配合物:合成,表征,晶体结构和DFT研究

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A new copper (II) Schiff base complex, CuL1, was prepared from the reaction of asymmetrical Schiff base ligand of L-1 and Cu(OAC)(2) (L-1 = salicylidene imino-ethylimino-pentan-2-one). The Schiff base ligand, and its copper (II) complex, CuL1, have been characterized by elemental analysis (CHN) and FT-IR and UV-vis spectroscopy. In addition, H-1 NMR was employed for characterization of the ligand. Thermogrametric analysis of the CuL1 reveals its thermal stability and its decomposition pattern shows that it is finally decomposed to the copper oxide (CuO). The crystal structure of CUL1 was determined by the single crystal X-ray analysis. The CuL1 complex crystallizes in the monoclinic system, with space group P2(1) and distorted square planar coordination around the metal ion. The Schiff base ligand of L-1 acts as a chelating ligand and coordinates via two nitrogen and two oxygen atoms to the copper (II) ion with C-1 symmetry. The structure of the CuL1 complex was also studied theoretically at different levels of DFT and basis sets. According to calculated results the C-O bond length of the salicylate fragment is slightly higher than that in the acetylacetonate fragment of ligand, which could be interpreted by resonance increasing between phenyl and chelated rings in ligand in relative to the acetylacetonate fragment. (C) 2014 Elsevier B.V. All rights reserved.
机译:由L-1的不对称Schiff碱配体与Cu(OAC)(2)反应制备了新的铜(II)Schiff碱配合物CuL1(L-1 =亚水杨基亚氨基亚乙基乙基亚氨基戊二-2-酮) 。 Schiff碱配体及其铜(II)配合物CuL1已通过元素分析(CHN)以及FT-IR和UV-vis光谱进行了表征。另外,采用H-1 NMR表征配体。对CuL1的热重分析表明其热稳定性,并且其分解模式表明其最终被分解为氧化铜(CuO)。通过单晶X射线分析确定CUL1的晶体结构。 CuL1配合物在单斜晶系系统中结晶,空间群为P2(1)/ n,金属离子周围的方形平面配位结构扭曲。 L-1的席夫碱配体充当螯合配体,并通过两个氮原子和两个氧原子与C-1对称的铜(II)离子配位。 CuL1配合物的结构也从理论上在不同水平的DFT和基础集上进行了研究。根据计算结果,水杨酸酯片段的C-O键长度略高于配体的乙酰丙酮酸酯片段中的C-O键长度,这可以通过相对于乙酰丙酮酸酯片段的配体中苯基和螯合环之间的共振增加来解释。 (C)2014 Elsevier B.V.保留所有权利。

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