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• W2022147623 abstract "Molecular dynamics simulations with separate thermostats for rotational and translational motion were used to study the effect of these degrees of freedom on the structure of water around model solutes. To describe water molecules we used the SPC/E model. The simplest solute studied here, the hydrophobe, was represented as a Lennard-Jones particle. Since direct interaction between the hydrophobe and water molecules has no angular dependence the influence of the increase of the rotational temperature on the solvation of a hydrophobe is only indirect. In the next step the central solute was assumed to be charged with either a positive or a negative charge to mimic an ion in water. Hence, depending on the charge of the ion, the neighboring water molecules assumed different angular distributions. The principal conclusions of this work are: (i) an increase of the translational temperature always decreases the height of the first peak in the solute-water radial distribution function; (ii) an increase of the rotational temperature yields an increase in the first peak in the solute-water radial distribution function for hydrophobes and cations; (iii) in contrast to this, the solvation peak decreases around ions with sufficiently large negative charge; and (iv) an increase of the rotational temperature affects cations in an opposite way to anions. For this reason complex molecules with a small net charge may not be very sensitive to variation of the rotational temperature." @default.
• W2022147623 created "2016-06-24" @default.
• W2022147623 creator A5009590488 @default.
• W2022147623 creator A5040099064 @default.
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• W2022147623 date "2014-05-14" @default.
• W2022147623 modified "2023-10-16" @default.
• W2022147623 title "Effects of the translational and rotational degrees of freedom on the hydration of simple solutes" @default.
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• W2022147623 doi "https://doi.org/10.1063/1.4875280" @default.
• W2022147623 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4032416" @default.
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