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[UO2(NH3)5]Br2 ∙ NH3 : synthesis, crystal structure, and speciation in liquid ammonia solution by first-principles molecular dynamics simulations

机译:[UO2(NH3)5] Br2·NH3:液态氨溶液的合成,晶体结构和形态的第一性原理分子动力学模拟

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摘要

Pentaammine dioxido uranium(VI) dibromide ammonia (1/1), [UO2(NH3)5]Br2·NH3, was synthesized in the form of yellow crystals by the reaction of uranyl bromide, UO2Br2, with dry liquid ammonia. The compound crystallizes orthorhombic in space group Cmcm and is isotypic to [UO2(NH3)5]Cl2·NH3 with a = 13.2499(2), b = 10.5536(1), c = 8.9126(1) Å, V = 1246.29(3) Å3 and Z = 4 at 123 K. The UO22+ cation is coordinated by five ammine ligands and the coordination polyhedron can be best described as pentagonal bipyramid. Car–Parrinello molecular dynamics simulations are reported for [UO2(NH3)5]2+ in the gas phase and in liquid NH3 solution (using the BLYP density functional). According to free-energy simulations, solvation by ammonia has only a small effect on the uranyl–NH3 bond strength.
机译:通过铀酰溴,UO2Br2与干燥的液态氨反应,合成了黄色晶体形式的五胺五氧化二铀(VI)二溴化氨(1/1),[UO2(NH3)5] Br2·NH3。该化合物在Cmcm空间群中结晶为正交晶,与[UO2(NH3)5] Cl2·NH3同型,a = 13.2499(2),b = 10.5536(1),c = 8.9126(1)Å,V = 1246.29(3 )在123 K时Å3和Z =4。UO22+阳离子由5个胺配体配位,配位多面体可以最好地描述为五角双锥。据报道,在气相和液态NH3溶液中[UO2(NH3)5] 2+的Car–Parrinello分子动力学模拟(使用BLYP密度泛函)。根据自由能模拟,氨的溶剂化对铀酰-NH3键强度的影响很小。

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