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微孔{[Ni(环瓜)]3[W(CN)8]2}n 提供了可逆的结构和磁性转变。

Microporous {[Ni(cyclam)]3[W(CN)8]2}n affording reversible structural and magnetic conversions.

机构信息

Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Kraków, Poland.

出版信息

Dalton Trans. 2011 Mar 28;40(12):3067-73. doi: 10.1039/c0dt01434f. Epub 2011 Feb 17.

DOI:10.1039/c0dt01434f
PMID:21331398
Abstract

Methanol adsorption into the porous 2D bimetallic coordination network {Ni(cyclam)W(CN)(8)}(n) (cyclam = 1,4,8,11-tetraazacyclotetradecane) causes significant modification of its structure and magnetic properties. Fully reversible transformations between the three states of the network: anhydrous, hydrated and methanol-modified are observed with the transition to the magnetic ordered state at T(c) equal to 4.9 K, 8.3 K and 11.4 K respectively. All three phases have a metamagnetic character but the methanol-modified one most easily turns to ferromagnetic and shows a hysteresis loop with coercivity field of 250 Oe. The differences in magnetic behaviour of the anhydrous and guest-induced forms of the compound are discussed in terms of changes in the structure: CN-bridge geometry and distance between the layers.

摘要

甲醇吸附到多孔二维双金属配位网络{Ni(cyclam)W(CN)(8)}(n)(cyclam=1,4,8,11-四氮杂环十四烷)中会显著改变其结构和磁性质。该网络的三种状态:无水、水合和甲醇修饰之间的完全可逆转变,分别在转变到磁有序态时观察到 T(c)等于 4.9 K、8.3 K 和 11.4 K。所有三个相都具有抗磁性,但甲醇修饰的相最容易转变为铁磁性,并显示出具有 250 Oe 矫顽力场的滞后环。无水和客体诱导化合物的磁行为差异是根据结构变化来讨论的:CN-桥几何形状和层之间的距离。

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