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首页> 外文期刊>Journal of Molecular Structure >Synthesis, characterization and catecholase-like activity of new Schiff base metal complexes derived from visnagin: Theoretical and experimental study
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Synthesis, characterization and catecholase-like activity of new Schiff base metal complexes derived from visnagin: Theoretical and experimental study

机译:visnagin衍生的新型Schiff贱金属配合物的合成,表征和儿茶酚酶样活性:理论和实验研究

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摘要

A new tetradentate, unsymmetrical Schiff base ligand (H2L) containing a donor set of N2O2 and its mononuclear Cu(II) and Fe(II) complexes ([CuL] and [FeL]), were synthesized and characterized on the basis of their elemental analysis, FT-IR, Raman, H-1 and C-13 NMR spectra, electronic and mass spectra, molar conductivity and magnetic susceptibility measurements. Density functional theory (DFT) calculations were performed in order to clarify molecular structures, 1H NMR and 13C NMR chemical shift values, frontier molecular orbitals (FMOs), nonlinear optical properties and map of molecular electrostatic potential (MEP) of the title molecules. In agreement with trials, the results provide a full explanation of the highest efficiency observed for the compounds in relation to the electronic and the structural characteristics. The catecholase-like activity of the complexes toward the oxidation of 3,5-ditert-butylcatechol (3,5-DTBC) to the corresponding quinone showed that both complexes have moderate catalytic activity. [FeL] shows higher activity (k(cat) = 26.4 h(-1)) than that of [CuL] (k(cat) = 23.4 h(-1)). (c) 2016 Elsevier B.V. All rights reserved.
机译:合成了一种新的四齿,不对称的席夫碱配体(H2L),该配体包含N2O2供体及其单核Cu(II)和Fe(II)配合物([CuL]和[FeL]),并根据其元素进行了表征分析,FT-IR,拉曼,H-1和C-13 NMR光谱,电子和质谱,摩尔电导率和磁化率测量。为了阐明分子结构,标题化合物的1H NMR和13C NMR化学位移值,前沿分子轨道(FMO),非线性光学性质和分子静电势图(MEP),进行了密度泛函理论(DFT)计算。与试验一致,结果充分说明了化合物在电子和结构特性方面观察到的最高效率。配合物对3,5-二叔丁基邻苯二酚(3,5-DTBC)氧化为相应醌的类儿茶酚酶活性表明,两种配合物均具有中等催化活性。 [FeL]的活性(k(cat)= 26.4 h(-1))比[CuL]的活性(k(cat)= 23.4 h(-1))高。 (c)2016 Elsevier B.V.保留所有权利。

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