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首页> 外文期刊>Polyhedron: The International Journal for Inorganic and Organometallic Chemistry >Metal coordination architectures of N-acyl-salicylhydrazides: The effect of metal ions and steric repulsion of ligands to their structures of polynuclear metal complexes
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Metal coordination architectures of N-acyl-salicylhydrazides: The effect of metal ions and steric repulsion of ligands to their structures of polynuclear metal complexes

机译:N-酰基-水杨酰肼的金属配位结构:金属离子和配体的空间排斥对其多核金属配合物结构的影响

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摘要

Three polynuclear transition metal complexes [Mn-8(DMF)(8)(L1)(8)] center dot 4DMF (1), [Mn-6(DMF)(6)(L2)(6)] center dot [Mn-6(DMF)(4)(H2O)(2)(L2)(6)] center dot 2DMF (2), [Cu-3(L3)(2)(py)(2)] (3) of the pentadentate ligands N-acyl-salicylhydrazides were synthesized and characterized, their crystal structures were investigated. The oxidation state and properties of the central metal ions are important in crystal structure formation, trivalent Mn(III) ion which easily form stable octahedral coordination metallamacrocycle complexes, metallacrowns 1 and 2 were obtained; while bivalent Cu(II) ion is easier to form square planar, trinuclear complexes 3 was obtained. The steric effect of the N-acyl side chains also plays an important role in the structures of these polynuclear complexes. The magnetic property of 1 was also investigated. (c) 2008 Elsevier Ltd. All rights reserved.
机译:三种多核过渡金属配合物[Mn-8(DMF)(8)(L1)(8)]中心点4DMF(1),[Mn-6(DMF)(6)(L2)(6)]中心点[Mn -6(DMF)(4)(H2O)(2)(L2)(6)]中心点2DMF(2),[Cu-3(L3)(2)(py)(2)](3)合成并表征了五齿配体N-酰基-水杨酰肼,并对其晶体结构进行了研究。中心金属离子的氧化态和性质在晶体结构形成中很重要,获得了易于形成稳定的八面体配位金属lamcrocrocycle配合物的三价Mn(III)离子,并获得了金属胎蛋白1和2。尽管二价Cu(II)离子更易于形成正方形平面,但获得了三核络合物3。 N-酰基侧链的空间效应在这些多核复合物的结构中也起重要作用。还研究了1的磁性。 (c)2008 Elsevier Ltd.保留所有权利。

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