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- W2912255011 abstract "The entropies of molecules in solution are often calculated using gas phase formulas. It is assumed that, because implicit solvation models are fitted to reproduce free energies, this is sufficient for modeling reactions in solution. However, this procedure exaggerates entropic effects in processes that change molecularity. Here, computationally efficient (i.e., having similar cost as gas phase entropy calculations) approximations for determining solvation entropy are proposed to address this issue. The Sω, Sϵ, and Sϵα models are nonempirical and rely only on physical arguments and elementary properties of the medium (e.g., density and relative permittivity). For all three methods, average errors as compared to experiment are within chemical accuracy for 110 solvation entropies, 11 activation entropies in solution, and 32 vaporization enthalpies. The models also make predictions regarding microscopic and bulk properties of liquids which prove to be accurate. These results imply that ΔHsol and ΔSsol can be described separately and with less reliance on parametrization by a combination of the methods presented here with existing, reparametrized, implicit solvation models." @default.
- W2912255011 created "2019-02-21" @default.
- W2912255011 creator A5024063229 @default.
- W2912255011 date "2019-03-26" @default.
- W2912255011 modified "2023-10-18" @default.
- W2912255011 title "Solvation Entropy Made Simple" @default.
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- W2912255011 doi "https://doi.org/10.1021/acs.jctc.9b00214" @default.
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