溴化锂
锂(药物)
化学
碘化锂
氯化锂
卤化物
无机化学
碘化物
溴化物
晶体结构
水合物
水溶液
氯化物
分子
结晶学
物理化学
有机化学
医学
物理
热交换器
电极
电解质
热力学
内分泌学
作者
J. Sohr,H. Schmidt,Wolfgang Voigt
标识
DOI:10.1107/s2053229618001183
摘要
For lithium halides, Li X ( X = Cl, Br and I), hydrates with a water content of 1, 2, 3 and 5 moles of water per formula unit are known as phases in aqueous solid–liquid equilibria. The crystal structures of the monohydrates of LiCl and LiBr are known, but no crystal structures have been reported so far for the higher hydrates, apart from LiI·3H 2 O. In this study, the crystal structures of the di- and trihydrates of lithium chloride, lithium bromide and lithium iodide, and the pentahydrates of lithium chloride and lithium bromide have been determined. In each hydrate, the lithium cation is coordinated octahedrally. The dihydrates crystallize in the NaCl·2H 2 O or NaI·2H 2 O type structure. Surprisingly, in the tri- and pentahydrates of LiCl and LiBr, one water molecule per Li + ion remains uncoordinated. For LiI·3H 2 O, the LiClO 4 ·3H 2 O structure type was confirmed and the H-atom positions have been fixed. The hydrogen-bond networks in the various structures are discussed in detail. Contrary to the monohydrates, the structures of the higher hydrates show no disorder.
科研通智能强力驱动
Strongly Powered by AbleSci AI