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A neutral 2D oxalate-based soluble magnet assembled by hydrogen bonding interactions

机译:通过氢键相互作用组装的中性2D草酸盐基可溶磁体

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Herein we describe the synthesis, structure and magnetic properties of a novel oxalate-based layered magnetic system: {[Mn(OH2)(2)(S)(2)][Mn(S)(OH2)](2)[Cr(ox)(3)](2)(18-crown-6)}(infinity) (S = CH3OH; ox = C2O42-; 18-crown-6 = C12H24O6) (1). In this case, no cationic templating agent is required to promote the assembling of low-dimensional oxalate-bridged metallic complexes in solution. Instead, strong enough hydrogen bonding interactions are responsible for their packing in the solid state. This magnet is soluble and presents two different types of oxalate bridges: the common bis(bidentate) and the unusual bidentate monodentate. This structural feature has drastic consequences on the magnetism of this compound, as it shows ferrimagnetic ordering below 5.5 K.
机译:在这里,我们描述了一种新型的草酸盐基层状磁性系统的合成,结构和磁性能:{[Mn(OH2)(2)(S)(2)] [Mn(S)(OH2)](2)[Cr (ox)(3)](2)(18-crown-6)}(无穷大)(S = CH 3 OH; ox = C 2 O 42-; 18-crown-6 = C 12 H 24 O 6)(1)。在这种情况下,不需要阳离子模板剂来促进低维草酸盐桥联的金属络合物在溶液中的组装。取而代之的是,足够强的氢键相互作用导致固态堆积。这种磁铁是可溶的,并呈现出两种不同类型的草酸盐桥:共同的双(双齿)和不寻常的双齿单齿。这种结构特征对该化合物的磁性产生了巨大影响,因为它显示出5.5 K以下的亚铁磁性有序。

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