首页> 外文期刊>Inorganica Chimica Acta >Synthesis, characterization, X-ray molecular structure and catalase-like activity of a non-heme iron complex: Dichloro[N-propanoate-N,N-bis-(2-pyridylmethyl)amine]iron(III)
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Synthesis, characterization, X-ray molecular structure and catalase-like activity of a non-heme iron complex: Dichloro[N-propanoate-N,N-bis-(2-pyridylmethyl)amine]iron(III)

机译:非血红素铁配合物:二氯[N-丙酸酯-N,N-双-(2-吡啶基甲基)胺]铁(III)的合成,表征,X射线分子结构和过氧化氢酶样活性

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In this work we present the synthesis and characterization of the complex dichloro[N-propanoate-N,N-bis-(2-pyridylmethyl)amine]iron(III) [Fe-III(PBMPA)Cl-2]. The ligand LiPBMPA was synthesized through the Michael reaction of BMPA with methylacrylate, followed by alkaline hydrolysis. The complex [Fe-III(PBMPA)Cl-2] has been synthesized by the reaction of the ligand with FeCl3 center dot H2O and was mainly characterized by cyclic voltammetry, conductivimetry, and electronic, infrared and Mossbauer spectroscopies, and by X-ray structural analysis, which showed an iron center coordinated by one carboxylate oxygen in a monodentate way, one tertiary amine, two pyridine groups and two chloride ions. It has been proposed that in water the chloride ligands are shifted by the solvent molecules and the species [Fe-III(PBMPA)(H2O)(2)]Cl-2 is predominant. The catalase-like activity of the complex was tested in water, and it proved to be active in the hydrogen peroxide dismutation. Kinetics studies were conducted following the initial rates method. The reaction is first order in relation to both the complex and the hydrogen peroxide. Based on the presence of a lag phase that depends on the initial complex concentration, we propose that the active species that shows in situ catalase-like activity, is a binuclear complex. (c) 2006 Elsevier B.V. All rights reserved.
机译:在这项工作中,我们介绍了二氯[N-丙酸酯-N,N-双-(2-吡啶基甲基)胺]铁(III)[Fe-III(PBMPA)Cl-2]的合成和表征。配体LiPBMPA是通过BMPA与丙烯酸甲酯的迈克尔反应,然后进行碱水解而合成的。配合物[Fe-III(PBMPA)Cl-2]是通过配体与FeCl3中心点H2O反应合成的,其主要特征在于循环伏安法,电导率法,电子,红外和莫斯鲍尔分光光度法以及X射线分析结构分析表明,铁中心由一个单齿方式的羧酸氧,一个叔胺,两个吡啶基和两个氯离子配位。已经提出,在水中氯化物配体被溶剂分子移动,并且种类[Fe-III(PBMPA)(H2O)(2)] Cl-2是主要的。在水中测试了该复合物的过氧化氢酶样活性,并证明其在过氧化氢歧化中具有活性。动力学研究是按照初始速率法进行的。该反应对于络合物和过氧化氢都是一级的。基于依赖于初始复合物浓度的滞后阶段的存在,我们建议显示原位过氧化氢酶样活性的活性物质是双核复合物。 (c)2006 Elsevier B.V.保留所有权利。

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