Predicting hydration Gibbs energies of alkyl-aromatics using molecular simulation

A comparison of current force fields and the development of a new parameter set for accurate solvation data

Nuno M. Garrido, Miguel Jorge, António J. Queimada, José R B Gomes, Ioannis Economou, Eugénia A. MacEdo

Research output: Contribution to journalArticle

13 Citations (Scopus)

Abstract

The Gibbs energy of hydration is an important quantity to understand the molecular behavior in aqueous systems at constant temperature and pressure. In this work we review the performance of some popular force fields, namely TraPPE, OPLS-AA and Gromos, in reproducing the experimental Gibbs energies of hydration of several alkyl-aromatic compounds - benzene, mono-, di- and tri-substituted alkylbenzenes - using molecular simulation techniques. In the second part of the paper, we report a new model that is able to improve such hydration energy predictions, based on Lennard Jones parameters from the recent TraPPE-EH force field and atomic partial charges obtained from natural population analysis of density functional theory calculations. We apply a scaling factor determined by fitting the experimental hydration energy of only two solutes, and then present a simple rule to generate atomic partial charges for different substituted alkyl-aromatics. This rule has the added advantages of eliminating the unnecessary assumption of fixed charge on every substituted carbon atom and providing a simple guideline for extrapolating the charge assignment to any multi-substituted alkyl-aromatic molecule. The point charges derived here yield excellent predictions of experimental Gibbs energies of hydration, with an overall absolute average deviation of less than 0.6 kJ mol -1. This new parameter set can also give good predictive performance for other thermodynamic properties and liquid structural information.

Original languageEnglish
Pages (from-to)17384-17394
Number of pages11
JournalPhysical Chemistry Chemical Physics
Volume13
Issue number38
DOIs
Publication statusPublished - 14 Oct 2011
Externally publishedYes

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Solvation
Gibbs free energy
Population Density
Benzene
Thermodynamics
Hydration
field theory (physics)
solvation
hydration
Carbon
Guidelines
Pressure
Temperature
simulation
energy
aromatic compounds
Aromatic compounds
predictions
Density functional theory
solutes

ASJC Scopus subject areas

  • Physics and Astronomy(all)
  • Physical and Theoretical Chemistry

Cite this

Predicting hydration Gibbs energies of alkyl-aromatics using molecular simulation : A comparison of current force fields and the development of a new parameter set for accurate solvation data. / Garrido, Nuno M.; Jorge, Miguel; Queimada, António J.; Gomes, José R B; Economou, Ioannis; MacEdo, Eugénia A.

In: Physical Chemistry Chemical Physics, Vol. 13, No. 38, 14.10.2011, p. 17384-17394.

Research output: Contribution to journalArticle

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