固溶体Co3.6Mg1.4Cl2(TeO3)4

R. Takagi, D. Hjelmqvist, M. Johnsson
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引用次数: 2

摘要

包含孤对元素的复杂过渡金属氧卤化物,如碲(IV),形成了一个有吸引力的研究领域,因为有很高的可能性发现新的低维排列的化合物,特别是低维排列的过渡金属子结构,导致有趣的物理性质。碲(IV)可以驱动许多不寻常结构的形成,因为它具有立体化学活性的孤对电子e。通常需要三个或四个氧原子配位才能形成TeO3E方形金字塔或TeO3+1E三角形双金字塔。这些孤对在降低晶体结构的维数方面起着非常重要的作用。先前对过渡金属碲(IV)氧化卤化物的研究揭示了一系列化合物,其中许多化合物表现出有趣的性质,例如磁挫败。本文的独特之处在于利用碱土元素(AE)来增强孤对元素的这种能力,从而降低过渡金属排列的维数。通过双重使用“化学剪刀”(与碱土元素结合使用的孤对元素),我们获得了新型的低维排列化合物。本文主要研究了五组分体系AE- teiv -TM- o -X (AE=碱土金属,TM=过渡金属,X=卤素)中一系列化合物的合成和表征,其中发现了9个新化合物。这些化合物的晶体结构都是由单晶x射线衍射数据确定的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The solid solution Co3.6Mg1.4Cl2(TeO3)4
Complex transition metals oxyhalides containing a lone pair element, such as tellurium (IV), form an attractive research field because there is a high probability of finding new low-dimensionally arranged compounds and, particularly, a low-dimensionally arranged transition metals substructures, leading to interesting physical properties. Tellurium (IV) can drive the formation of many unusual structures because of its stereochemically active lone pair electrons, E. It commonly takes a coordination of three or four oxygen atoms to form either a TeO3E square pyramid or a TeO3+1E trigonal bipyramid. These lone pairs are very important players involved in lowering the dimensionality of crystal structures. Previous studies in transition metal tellurium (IV) oxohalide quarternary systems revealed a family of compounds, many of which exhibit interesting properties e.g. magnetic frustration. The unique point of this thesis is to employ alkaline earth elements (AE) to augment this ability of lone pair elements to lower the dimensionality of the transition metal arrangements. By this double usage of “chemical scissors” (a lone pair element used in conjunction with alkaline earth elements) we obtained new types of low-dimensionally arranged compounds.This thesis is focused on the syntheses and characterization of a series of compounds in the pentanary (five components) system AE-TeIV-TM-O-X (AE=alkaline earth metal, TM=transition metal and X=halogen), in which nine new compounds were found. The crystal structures of each of these compounds were determined by the single crystal X-ray diffraction data.
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