Isotope Effects for Lattice Strain and Pseudo Jahn-Teller Distortion of Chiral Cyanide-Bridged Cu(II)-Co(III), Cr(III), and Fe(III) Bimetallic Assemblies

T. Akitsu, Satoru Sonoki
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引用次数: 2

Abstract

By substituting H/D and 18 O isotopes of water molecules, we prepared co-crystals of one-dimensional cyanide- bridged Cu(II)-Cr(III), Cu(II)-Co(III), and Cu(II)-Fe(III) bimetallic assemblies and mononuclear Cu(II) complexes, (CuL2)3(M(CN)6)2·4H2O (L = trans-cyclohexane-(1R, 2R)-diamine; M = Cr, Co, and Fe). Solid state CD and diffuse re- flectance electronic spectra exhibited typical difference of metal ions and little isotope effects. While H/D isotope effects emerged as differences of small intermolecular magnetic interactions and obvious shifts of IR bands. Though all com- pounds exhibited positive thermal expansion of lattice, crystal structures exhibited slight differences associated with Jahn- Teller distortion around Cu(II) coordination environment.
手性氰化物桥接Cu(II)-Co(III), Cr(III)和Fe(III)双金属组合物晶格应变和伪Jahn-Teller畸变的同位素效应
通过取代水分子的H/D和18o同位素,我们制备了一维氰化物桥接Cu(II)- cr (III)、Cu(II)- co (III)和Cu(II)- fe (III)双金属组合物和单核Cu(II)配合物(CuL2)3(M(CN)6)2·4H2O (L =反式环己烷-(1R, 2R)-二胺;M = Cr, Co和Fe)。固态CD和漫反射电子能谱表现出典型的金属离子差异和较小的同位素效应。H/D同位素效应表现为分子间小磁相互作用的差异和红外波段的明显偏移。虽然所有的化合物都表现出晶格的正热膨胀,但在Cu(II)配位环境下,晶体结构表现出与Jahn- Teller畸变相关的微小差异。
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