首页> 外文期刊>Inorganica Chimica Acta >Synthesis, crystal structure, spectral properties and catalytic activity of hexakis(imidazole)manganese(II) bisindole-2-carboxylato bisneocuproine bisdimethyl sulfoxide solvates {[Mn-II(Im)(6)] center dot 2(2-IC) center dot 2(NC) center dot 2(DMSO)}
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Synthesis, crystal structure, spectral properties and catalytic activity of hexakis(imidazole)manganese(II) bisindole-2-carboxylato bisneocuproine bisdimethyl sulfoxide solvates {[Mn-II(Im)(6)] center dot 2(2-IC) center dot 2(NC) center dot 2(DMSO)}

机译:六(咪唑)锰(II)双吲哚-2-羧基双-新新星嘌呤双二甲基亚砜溶剂化物[[Mn-II(Im)(6)]中心点2(2-IC)中心点的合成,晶体结构,光谱性质和催化活性2(NC)中心点2(DMSO)}

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Synthesis, X-ray crystal structure and IR spectrum of {[Mn-II(Im)(6)]center dot 2(2-IC)center dot 2(NC)center dot 2(DMSO)} (Im = imidazole, 2-HIC = indole-2-carboxylic acid, NC = 2,9-dimethyl-1,10-phenanthroline, DMSO = dimethyl sulfoxide) are reported. The manganese(II) ion has octahedral geometry with a MnN6 core. The crystal structure is completed by two NC, two 2-IC- and two DMSO solvate molecules. The individual cations are linked into chains running parallel to the a axis by four intermolecular hydrogen bonding involving two 2-IC- solvate. Moreover, these chains are connected by pi-pi stacking interactions which occur between neocuproine molecules related through inversion center. In IR spectroscopy, the compound spectrum is roughly similar to the imidazole one: (i) above 1800 cm(-1), the bands are broad, but when focussing on some of them a doublet structure can be found; (ii) below 1800 cm(-1), the bands are sharp and it is then possible to point out the modification of S-O band when this later is involved in bifurcated hydrogen bonding to a second solvate 2-IC-. The compound catalyses the disproportionation of H2O2; moreover an additional quantity of imidazole increases the reaction rate. (c) 2006 Elsevier B.V. All rights reserved.
机译:{[Mn-II(Im)(6)]中心点2(2-IC)中心点2(NC)中心点2(DMSO)}的合成,X射线晶体结构和红外光谱(Im =咪唑,2报告了-HIC =吲哚-2-羧酸,NC = 2,9-二甲基-1,10-菲咯啉,DMSO =二甲基亚砜。锰离子具有MnN6核的八面体几何形状。晶体结构由两个NC,两个2-IC-和两个DMSO溶剂化物分子完成。各个阳离子通过涉及两个2-IC-溶剂化物的四个分子间氢键连接成与a轴平行的链。而且,这些链通过在通过反转中心相关的新环丙氨酸分子之间发生的pi-pi堆积相互作用而连接。在红外光谱中,化合物的光谱与咪唑大致相似:(i)在1800 cm(-1)以上,谱带较宽,但当聚焦于其中一些时,可发现双峰结构; (ii)在1800 cm(-1)以下,谱带很锋利,然后有可能指出S-O谱带的修饰,这是因为后者稍后参与了与第二个溶剂化物2-IC-的氢分叉。该化合物催化过氧化氢的歧化。此外,额外的咪唑量可提高反应速率。 (c)2006 Elsevier B.V.保留所有权利。

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