Isotope Effect and Lanthanide Contraction for 3d-4f Cyanide-Bridged Complexes Exhibiting Negative Thermal Expansion

Yusuke Kimoto, Takeshi Matsui, T. Akitsu
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引用次数: 1

Abstract

We have prepared some 3d-4f cyanide-bridged Ln(DMF)4(H2O)3Fe(CN)6•H2O complexes (Ln = Ce, Sm, Nd, and Gd; DMF = N,N-dimethylformamide) by substituting isotopes to 2 H-substituted H2O and DMF and 18 O-substituted H2O (and normal 1 H- and 16 O-H2O or 1 H-DMF). We examined their crystal structures exhibiting negative thermal expansion and compared in view of hydrogen bonds and lanthanide contraction. Magnetic properties and thermal analysis exhibited importance of intermolecular hydrogen bonds in crystal lattice for this behavior. While Fe2p3/2 and Fe2p1/2 XAS indicated constant inner shell electron states of low-spin Fe(III) ions.
负热膨胀的3d-4f氰化物桥配合物的同位素效应和镧系元素收缩
我们制备了一些3d-4f氰化物桥接的Ln(DMF)4(H2O)3Fe(CN)6•H2O配合物(Ln = Ce, Sm, Nd, Gd;DMF = N,N-二甲基甲酰胺),通过将同位素取代为2 H取代的H2O和DMF和18 o取代的H2O(以及正常的1 H-和16 O-H2O或1 H-DMF)。我们检查了它们的晶体结构表现为负热膨胀,并从氢键和镧系元素收缩的角度进行了比较。磁性能和热分析表明,分子间氢键在晶体晶格中的作用。而Fe2p3/2和Fe2p1/2 XAS显示出低自旋Fe(III)离子的恒定内层电子态。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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