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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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摘要

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 μ = 3.10 μB for the Fe2+ complex suggesting it has a trigonal bipyramidal coordination geometry, matching the crystal structure of the Cu2+ complex, while the μ = 5.52 μB value for the Mn2+ complex suggests it is high spin octahedral. Cyclic voltammetry in acetonitrile revealed reversible redox processes in all three complexes, suggesting 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.
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Mn 2 + ,Fe 2 + 和Cu 2 + 阳离子。获得了双质子化配体及其Cu 2 + 配合物的X射线晶体结构,表明该配体的五齿结合具有侧桥Cyclam环的反式II构型,并留下了潜在的不稳定结合位点吡啶供体上的化合物用于配合物与氧化剂和/或底物的相互作用。这些配合物的电子性质是通过固态磁矩确定的,Fe 2 + 配合物的μ= 3.10μB低,表明它具有三角双锥体配位几何,与晶体匹配Cu 2 + 配合物的结构,而Mn 2 + 配合物的μ= 5.52μB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。以过氧化氢为末端氧化剂进行氧化催化的筛选确定了Fe 2 + 配合物是最值得继续开发的氧化催化剂。

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