HBF4的气相酸度(HF-BF3)

PhysChemComm Pub Date : 1999-01-01 DOI:10.1039/A907705G
A. Otto
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引用次数: 1

摘要

利用高精度能量模型[CBS-4, CBS-Q, CBS-QB3, G1, G2(MP2)和G2]以及密度泛函B3LYP形式,从头计算了配合超强酸HBF4的气相酸度、BF3与HF的相互作用以及F-与BF4-的分离。除了CBS-4和G1之外,所有方法都提供了几乎相等的气相酸度数据,人们可能会推荐吉布斯自由能为288-289 kcal mol-1,相应的298k焓为291-292 kcal mol-1。配合物HF-BF3在真空中是不稳定的,因为根据所用方法的不同,分解成HF和BF3的吉布斯自由能预计在-3.6和-4.6 kcal mol-1之间。共轭碱BF4-对氟离子脱离是稳定的。我们推荐的焓和吉布斯自由能分别为81 ~ 82 kcal mol-1和72 ~ 73 kcal mol-1。
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The gas phase acidity of HBF4 (HF-BF3)
The gas phase acidity of the complex superacid HBF4 and the interaction of BF3 with HF as well as the F- detachment from BF4- have been calculated ab initio using high accuracy energy models [CBS-4, CBS-Q, CBS-QB3, G1, G2(MP2) and G2] as well as the density functional B3LYP formalism. All methods but CBS-4 and G1 provide practically equal acidity data for the gas phase and one may recommend 288-289 kcal mol-1 for the Gibbs free energy and 291-292 kcal mol-1 for the corresponding enthalpy at 298 K. The complex HF-BF3 is unstable in vacuo as the Gibbs free energy of decomposition into HF and BF3 is predicted to be between -3.6 and -4.6 kcal mol-1 depending on the method used. The conjugated base BF4- is stable with respect to fluoride ion detachment. We recommend 81-82 kcal mol-1 and 72-73 kcal mol-1 for the enthalpy and the Gibbs free energy, respectively.
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