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前所未有的氧代钛柠檬酸盐络合物从柠檬酸盐水溶液中沉淀出来,呈现出一种新型的双层Ti8O10结构核心。

Unprecedented oxo-titanium citrate complex precipitated from aqueous citrate solutions, exhibiting a novel bilayered Ti8O10 structural core.

作者信息

Kemmitt Tim, Al-Salim Najeh I, Gainsford Graeme J, Bubendorfer Andrea, Waterland Mark

机构信息

Industrial Research Ltd., P.O. Box 31-310, Lower Hutt, New Zealand.

出版信息

Inorg Chem. 2004 Oct 4;43(20):6300-6. doi: 10.1021/ic049760r.

Abstract

Aqueous titanium citrate solutions were prepared from the reaction of citric acid with titanium 2-propoxide in a range of molar ratios. Solutions containing two or fewer citrates per titanium resulted in the slow crystallization of an insoluble titanium oxo-citrate complex. Single-crystal X-ray analysis identified the species as Ti(8)O(10)(citrate)(4)(H(2)O)(12).14H(2)O.3HOPr(i)(), crystallized in the tetragonal space group I4(1)/a, with a = 30.775(7) A, c = 14.528(7) A, V = 13 759(8) A(3), and Z = 8. The trianionic citrate ligands supply both carboxylate and alkoxide coordination and stabilize the structure using simultaneous chelating and bridging modes of attachment. The compound is a neutral species, exhibiting titanium in three contrasting environments. Laser Raman microscopy and (13)C CPMAS solid-state NMR data were consistent with those of the X-ray crystal structure. When exposed to air, the crystals rapidly lost water and became a powder. The dehydrated powder was noncrystalline to X-rays and insoluble, but (13)C NMR results demonstrated retention of the carboxylate linkages.

摘要

通过柠檬酸与异丙醇钛按一系列摩尔比反应制备了柠檬酸钛水溶液。每个钛含两个或更少柠檬酸盐的溶液导致一种不溶性氧代柠檬酸钛络合物缓慢结晶。单晶X射线分析确定该物种为Ti(8)O(10)(柠檬酸盐)(4)(H(2)O)(12).14H(2)O.3HOPr(i)(),结晶于四方空间群I4(1)/a中,a = 30.775(7) Å,c = 14.528(7) Å,V = 13 759(8) Å(3),Z = 8。三阴离子柠檬酸盐配体提供羧酸盐和醇盐配位,并通过同时的螯合和桥连连接模式稳定结构。该化合物是一种中性物种,钛在三种不同环境中呈现。激光拉曼显微镜和(13)C CPMAS固态NMR数据与X射线晶体结构的数据一致。暴露于空气中时,晶体迅速失去水分并变成粉末。脱水粉末对X射线无定形且不溶,但(13)C NMR结果表明羧酸盐键得以保留。

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