首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Synthesis and characterization of a bis-mu,eta(1)-carboxylate-bridged dinuclear manganese(II) complex containing a tetradentate tripodal ligand, N-(benzimidazol-2-ylmethyl)iminodiacetic acid
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Synthesis and characterization of a bis-mu,eta(1)-carboxylate-bridged dinuclear manganese(II) complex containing a tetradentate tripodal ligand, N-(benzimidazol-2-ylmethyl)iminodiacetic acid

机译:含四齿三脚架配体N-(苯并咪唑-2-基甲基)亚氨基二乙酸的双-mu,eta(1)-羧酸桥联双核锰(II)配合物的合成与表征

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摘要

The dinuclear Mn(II) complex, [Mn-2(Hbida)(2)(H2O)(2)], was prepared using a tetradentate tripodal ligand, N-(benzimidazol-2-ylmethyl)iminodiacetic acid (H(3)bida) which has two carboxylate and one benzimidazole groups. The manganese ions are doubly bridged using mu,eta(1)-bridging monodentate carboxylate oxygen atoms. The Mn-Mn bond distance of 3.446 angstrom in the complex is comparable to that observed in the active site of the native manganese arginase enzyme (3.30 angstrom). The geometry of the complex with four carboxylates in two different types of binding modes, non-bridging monodentate and mu,eta(1)-type bridging monodentate, mimics the active site structure of manganese arginase. The magnetic properties of the complex show a coupling constant of J = -0.471(1) cm(-1), which is consistent with weakly coupled antiferromagnetic Mn-II (S = 5/2) centers. The cyclic voltammograms of the Mn(II) complex in DMF show irreversible oxidation occurring around 570 mV (versus Ag/AgCl). (C) 2007 Elsevier Ltd. All rights reserved.
机译:使用四齿三脚架配体N-(苯并咪唑-2-基甲基)亚氨基二乙酸(H(3))制备双核Mn(II)配合物[Mn-2(Hbida)(2)(H2O)(2)]。具有两个羧酸盐和一个苯并咪唑基团。锰离子使用mu,eta(1)桥连单齿羧酸盐氧原子双桥联结。复合物中的Mn-Mn键距为3.446埃,与在天然锰精氨酸酶的活性位点(3.30埃)中观察到的相当。具有四种羧酸盐的复合物的几何结构以两种不同类型的结合模式(非桥连单齿和mu,eta(1)型桥连单齿)模拟锰精氨酸酶的活性位点结构。该复合物的磁性能显示出耦合常数J = -0.471(1)cm(-1),与弱耦合反铁磁Mn-II(S = 5/2)中心一致。 DMF中Mn(II)配合物的循环伏安图显示,发生约570 mV(相对于Ag / AgCl)的不可逆氧化。 (C)2007 Elsevier Ltd.保留所有权利。

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