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Synthesis, structural studies, and oxidation catalysis of the manganese(II), iron(II), and copper(II) complexes of a 2-pyridylmethyl pendant armed side-bridged cyclam

机译:2-吡啶基甲基悬挂侧桥环己酰胺的锰(II),铁(II)和铜(II)配合物的合成,结构研究和氧化催化

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The first 2-pyridylmethyl pendant armed structurally reinforced cyclam ligand has been synthesized and successfully complexed to Mn2+, Fe2+, and Cu2+ cations. X-ray crystal structures were obtained for the diprotonated ligand and its Cu2+ complex demonstrating pentadentate binding of the ligand with trans-II configuration of the side-bridged cyclam ring, leaving a potential labile binding site cis to the pyridine donor for interaction of the complex with oxidants and/or substrates. The electronic properties of these complexes were determined by means of solid state magnetic moment, with a low value of mu = 3.10 mu(B) for the Fe2+ complex suggesting that it has a trigonal bipyramidal coordination geometry, matching the crystal structure of the Cu2+ complex, while the mu = 5.52 mu(B) value for the Mn2+ complex suggests that it is high spin octahedral. Cyclic voltammetry in acetonitrile revealed reversible redox processes in all three complexes, suggesting that catalytic reactivity involving electron transfer processes are possible for these complexes. Screening for oxidation catalysis using hydrogen peroxide as the terminal oxidant identified the Fe2+ complex as the oxidation catalysts most worthy of continued development. (C) 2015 Elsevier B.V. All rights reserved.
机译:合成了第一个2-吡啶基甲基侧基武装的结构增强的cyclam配体,并成功与Mn2 +,Fe2 +和Cu2 +阳离子络合。获得了双质子化配体及其Cu2 +配合物的X射线晶体结构,表明配体具有侧桥cyclam环的反式II结构的五齿结合,为吡啶配位体留下了潜在的不稳定结合位点顺式,用于配合物的相互作用与氧化剂和/或底物。这些配合物的电子性质是通过固态磁矩确定的,Fe2 +配合物的mu = 3.10 mu(B)低,这表明它具有三角双锥体配位几何形状,与Cu2 +配合物的晶体结构匹配,而Mn2 +复合物的mu = 5.52 mu(B)值表明它是高自旋八面体。乙腈中的循环伏安法揭示了所有三种配合物中的可逆氧化还原过程,表明这些配合物可能涉及涉及电子转移过程的催化反应性。使用过氧化氢作为末端氧化剂的氧化催化筛选确定了Fe2 +络合物为最值得继续开发的氧化催化剂。 (C)2015 Elsevier B.V.保留所有权利。

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