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首页> 外文期刊>New Journal of Chemistry >Tacticity versus dimension of the extended structures in the crystals of heterospin magnets made of transition-metal complexes with the poly(aminoxyl) radical
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Tacticity versus dimension of the extended structures in the crystals of heterospin magnets made of transition-metal complexes with the poly(aminoxyl) radical

机译:由过渡金属配合物与聚(氨氧基)基组成的异旋磁体的晶体中立构规整度与尺寸的关系

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摘要

Bis- and tris(aminoxyl) radicals and di(4-pyridyl)diazomethane form crystalline complexes with extended structures upon reaction with [M(hfac)(2)] (M = Mn-II or Cu-II and hfac = hexafluoroacetylacetonate). Organic 2p and metal 3d spins in these complexes order at 3.4-46 K depending on the dimensions of the extended structures and the magnitude of exchange coupling between the adjacent spins. In the crystals of one-dimensional systems, the polymeric chains are isotactic in that free radical or precursor ligands and/or metal centres have the same chirality along any given chain. The polymeric chains are syndiotactic and cross link to form two-dimensional honeycomb or three-dimensional crossed parallel networks. [References: 47]
机译:与[M(hfac)(2)]反应后,双和三(氨基甲苯基)自由基和二(4-吡啶基)重氮甲烷形成具有扩展结构的晶体配合物(M = Mn-II或Cu-II,hfac =六氟乙酰丙酮酸酯)。这些络合物中的有机2p和金属3d自旋在3.4-46 K范围内,这取决于扩展结构的尺寸和相邻自旋之间交换耦合的大小。在一维系统的晶体中,聚合物链是全同立构的,其中自由基或前体配体和/或金属中心沿任何给定链具有相同的手性。聚合物链是间同的和交联的,以形成二维蜂窝或三维交叉平行网络。 [参考:47]

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