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Synthesis, structure and magnetic properties of a new family of chiral metal(II) citramalates

机译:新型手性金属柠檬酸酯的合成,结构和磁性

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A new series of chiral carboxylate-bridged complexes of Mn(II), Co(II), and Ni(II) has been synthesized by reaction of M(11) salts with (S)-2-hydroxy-2-methyl-butanedioic acid ((S)-citramalic acid) under solvothermal conditions. The Mn(II) compound I is obtained as a crystalline powder, whereas the Co(II) and Ni(II) compounds (2 and 3 respectively) are obtained as single crystals. All the compounds crystallize in orthorhombic chiral space group P2(1)2(1)2(1). Compounds 2 and 3 are isostructural, and their structure consists in helicoidal chains of M(II) centres linked by carboxylate bridges. The magnetic data indicate a rather weak coupling interaction between paramagnetic centres. The Mn(II) compound 1 exhibits antiferromagnetic ordering at T-N = 2.64 K. The Co(II) and Ni(II) compounds show ferromagnetic interactions within the chains. For 3, the chains couple antiferromagnetically, which leads to a metamagnetic behaviour with TN = 1.69 K. (c) 2006 Elsevier B.V. All rights reserved.
机译:M(11)盐与(S)-2-羟基-2-甲基丁二酸反应合成了一系列新的手性羧酸桥联的Mn(II),Co(II)和Ni(II)配合物溶剂热条件下的酸((S)-柠檬酸)。以结晶粉末形式获得Mn(II)化合物I,而以单晶形式获得Co(II)和Ni(II)化合物(分别为2和3)。所有化合物在正交晶体手性空间群P2(1)2(1)2(1)中结晶。化合物2和3是同构的,它们的结构由通过羧酸盐桥连接的M(II)中心的螺旋链组成。磁数据表明顺磁中心之间的耦合耦合作用很弱。 Mn(II)化合物1在T-N = 2.64 K时显示反铁磁有序。Co(II)和Ni(II)化合物在链内显示铁磁相互作用。对于3,链反铁磁耦合,从而导致TN = 1.69 K的超磁行为。(c)2006 Elsevier B.V.保留所有权利。

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