MTiF6·6H2O (M = Mn, Co, Ni, Zn)晶体中的氢O-H⋯F键

IF 1.2 4区 化学 Q4 CHEMISTRY, INORGANIC & NUCLEAR Journal of Structural Chemistry Pub Date : 2024-12-02 DOI:10.1134/S002247662411009X
A. A. Udovenko, E. B. Merkulov, D. Kh. Shlyk, N. M. Laptash
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引用次数: 0

摘要

合成了二价氟钛酸盐MTiF6·6H2O (M = Mn, Co, Ni, Zn)六水合物单晶。它们的晶体结构由室温下(rt结构)和相变下(LT结构)的x射线衍射确定。相变伴随着无序三角晶格向有序单斜晶格的转变。最初的rt结构在O-H⋯F氢键的集合和强度上有所不同,氢键将分离的[M(H2O)6]2+和[TiF6]2 -八面体连接成一个3D框架。氢键的强度与配合物的热行为之间存在相关性。
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Hydrogen O–H⋯F Bonds in the Crystals of MTiF6·6H2O (M = Mn, Co, Ni, Zn)

Single crystals of hexahydrates of divalent fluoridotitanates MTiF6·6H2O (M = Mn, Co, Ni, Zn) are synthesized. Their crystal structures are determined by X-ray diffraction at room temperature (RT-structure) and below the phase transition (LT structure). The phase transition is accompanied by a transformation of the disordered trigonal lattice into the ordered monoclinic one. The initial RT-structures differ in the set and strength of O–H⋯F hydrogen bonds linking isolated [M(H2O)6]2+ and [TiF6]2– octahedra into a 3D framework. There is a correlation between the strength of hydrogen bonds and the thermal behavior of the complexes.

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来源期刊
Journal of Structural Chemistry
Journal of Structural Chemistry 化学-无机化学与核化学
CiteScore
1.60
自引率
12.50%
发文量
142
审稿时长
8.3 months
期刊介绍: Journal is an interdisciplinary publication covering all aspects of structural chemistry, including the theory of molecular structure and chemical bond; the use of physical methods to study the electronic and spatial structure of chemical species; structural features of liquids, solutions, surfaces, supramolecular systems, nano- and solid materials; and the crystal structure of solids.
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