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Structure of a Hydrated Sulfonatotitanyl(IV) Complex in Aqueous Solution and the Dimethylsulfoxide Solvated Titanyl(IV) Ion in Solution and Solid State

机译:水溶液中水合磺化钛基(IV)配合物的结构和溶液和固态中二甲基亚砜溶剂化的钛基(IV)离子

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摘要

The coordination chemistry of oxotitanium(IV) or titanyl(IV), TiO2+, has been studied in solution by X-ray methods. The titanyl(IV) ion hydrolyzes easily in aqueous systems to solid titanium dioxide as long as it is not stabilized through complexation. In this study the structures of the hydrated bissulfatotitanyl(IV) complex and the dimethylsulfoxide (DMSO) solvated titanyl(IV) ions have been determined. In isolated monomeric titanyl complexes titanium(IV) binds strongly to a doubly bound oxo group at ca. 1.64 Å, to four ligands in the equatorial plane almost perpendicular to the Ti=O bond at ca. 2.02 Å, and there is one weakly bound ligand, trans to the Ti=O bond, at ca. 2.22 Å, for oxygen donor ligands; the O=Ti–Oeq bond angles are 95°–100°. The structure of the DMSO solvated titanyl(IV) ion in the solid state is maintained in DMSO solution.Electronic supplementary materialThe online version of this article (doi:10.1007/s10953-017-0581-3) contains supplementary material, which is available to authorized users.
机译:通过X射线方法研究了溶液中氧钛(IV)或氧钛(IV)的配位化学性质TiO 2 + 。钛氧基(IV)离子在水性体系中容易水解成固体二氧化钛,只要它不能通过络合稳定。在这项研究中,已确定了水合双硫代硫酸钛(IV)配合物和二甲基亚砜(DMSO)溶剂化的钛(IV)离子的结构。在分离的单体钛氧烷基络合物中,钛(IV)在约2-6处与双键结合的氧代基团牢固结合。 1.64Å,在赤道平面内几乎垂直于Ti = O键的四个配体2.02Å,并且在ca处有一个弱结合的配体,与Ti = O键相反。 2.22Å,用于氧供体配体; O = Ti–Oeq键角为95°–100°。在DMSO溶液中保持固态的DMSO溶剂化钛氧基(IV)离子的结构。电子补充材料本文的在线版本(doi:10.1007 / s10953-017-0581-3)包含补充材料,可用于授权用户。

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