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The new molybdenum(V) complexes with differently N-substituted beta '-hydroxy-beta-enaminones

机译:具有不同N取代的β'-羟基-β-烯胺酮的新型钼(V)配合物

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Six new dinuclear complexes of molybdenum(V) have been prepared by the reaction of [Mo2O3(acac)(4)] (acac = acetylacetonate ion) with the polydentate ligands, (beta'-hydroxy-beta-enaminones. The complexes are coordinated by two enaminone ligands via two donor oxygen atoms as in the analogous [beta-diketonates. The octahedral coordinations around the molybdenum atoms are completed by the monodentate solvent molecules D (methanol, ethanol, 2-propanol). The complexes of the general formulae [Mo2O4L2(ROH)(2)] . 2ROH (complex 1b) and [Mo2O4L2(ROH)(2)] . ROH (complex 2a) were easily losing solvated alcohol molecules. All complexes were characterized by elemental analysis, IR, and some of them by one- and two-dimensional NMR spectra (in case 1a) and by X-ray crystallography (1a, 1b and 2a). (C) 2003 Elsevier B.V. All rights reserved. [References: 21]
机译:通过[Mo2O3(acac)(4)](acac =乙酰丙酮离子)与多齿配体(β'-羟基-β-烯胺酮)反应制备了六个新的钼(V)双核配合物。由两个烯胺配体通过两个供体氧原子像在类似的[β-二酮酸酯]中形成。围绕钼原子的八面体配位是由单齿溶剂分子D(甲醇,乙醇,2-丙醇)完成的。 Mo2O4L2(ROH)(2)]。2ROH(配合物1b)和[Mo2O4L2(ROH)(2)]。ROH(配合物2a)容易丢失溶剂化的醇分子,所有配合物的特征在于元素分析,红外光谱和一些通过一维和二维NMR光谱(在情况1a中)和X射线晶体学(在1a,1b和2a中)对其进行分析(C)2003 Elsevier BV保留所有权利[参考文献:21]

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