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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Synthesis, crystal structure and catalytic activity for H2O2 disproportionation of the manganese(II) coordination polymer {[Mn(O2C(CF2)(8)CO2)(phen)(2)]H2O}(n) (phen=1,10-phenanthroline)
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Synthesis, crystal structure and catalytic activity for H2O2 disproportionation of the manganese(II) coordination polymer {[Mn(O2C(CF2)(8)CO2)(phen)(2)]H2O}(n) (phen=1,10-phenanthroline)

机译:锰(II)配位聚合物{[Mn(O2C(CF2)(8)CO2)(phen)(2)] H2O}(n)(phen = 1,10-菲咯啉

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摘要

The title polymeric complex {[Mn(O2C(CF2)(8)CO2)(phen)(2)]H2O), was synthesized through the reaction of 1,10-phenanthroline, perfluorosebacic acid and MnCO3 center dot H2O. The molecular structure was characterized by X-ray diffraction, elemental analysis, thermal gravimetry, IR and UV-Vis spectroscopy and its catalytic activity has been studied. X-ray structure analysis shows that each Mn(II) ion is octahedrally coordinated by two bidentate phenanthroline ligands and the carboxylate oxygen atoms from two symmetry related per-fluorosebacate ligands, which are coordinated in cisoid positions. The structure consists of polymeric chains, with the perfluorosebacato ligand bridging the Mn(II) ions in a monodentate fashion. Crystallographic characterization shows a supramolecular structure involving hydrogen bonds, pi-pi and pi-ring interactions. The catalytic results indicated that the complex has reasonably good activity towards the disproportionation. of hydrogen peroxide into water and dioxygen in methanol and it does not exhibit saturation kinetics with the substrate. The initial reaction rates and their temperature and base dependencies were investigated by monitoring the dioxygen evolution. Kinetic studies revealed a first-order dependence on the catalyst concentration. Activation parameters have been calculated at 301 K. (c) 2008 Elsevier Ltd. All rights reserved.
机译:通过1,10-菲咯啉,全氟癸二酸和MnCO3中心点H2O反应合成了标题聚合物配合物{[Mn(O2C(CF2)(8)CO2)(phen)(2)] H2O)。通过X射线衍射,元素分析,热重分析,IR和UV-Vis光谱对分子结构进行了表征,并对其催化活性进行了研究。 X射线结构分析表明,每个Mn(II)离子都由两个双齿菲咯啉配体和两个对称的全氟癸二酸酯配体的羧酸氧原子进行八面体配位,并在顺式甾体位置进行配位。该结构由聚合物链组成,全氟癸二酸配体以单齿方式桥接Mn(II)离子。晶体学表征显示涉及氢键,π-π和π-环相互作用的超分子结构。催化结果表明该配合物对歧化具有相当好的活性。将过氧化氢分解成水和甲醇中的双氧,它对底物没有表现出饱和动力学。通过监测双氧的释放来研究初始反应速率及其温度和碱依赖性。动力学研究揭示了对催化剂浓度的一级依赖性。激活参数的计算值为301K。(c)2008 ElsevierLtd。保留所有权利。

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