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• W2010052871 endingPage "012004" @default.
• W2010052871 startingPage "012004" @default.
• W2010052871 abstract "Studies of ion-water systems at condensed phase and at interfaces have pointed out that molecular and ionic polarization plays an important role for many phenomena ranging from hydrogen bond dynamics to water interfaces' structure. Classical and ab initio Molecular Dynamics simulations reveal that induced dipole moments at interfaces (e.g. air-water and water-protein) are usually high, hinting that polarizable models to be implemented in classical force fields should be very accurate in reproducing the electrostatic properties of the system. In this paper the electrostatic properties of three classical polarizable models for ion-water interaction are compared with ab initio results both at gas and condensed phase. For Li+- water and Cl--water dimers the reproducibility of total dipole moments obtained with high level quantum chemical calculations is studied; for the same ions in liquid water, Car-Parrinello Molecular Dynamics simulations are used to compute the time evolution of ionic and molecular dipole moments, which are compared with the classical models. The PD2-H2O model developed by the author and coworkers [Masia et al. J. Chem. Phys. 2004, 121, 7362] together with the gaussian intermolecular damping for ion-water interaction [Masia et al. J. Chem. Phys. 2005, 123, 164505] showed to be the fittest in reproducing the ab initio results from gas to condensed phase, allowing for force field transferability." @default.
• W2010052871 created "2016-06-24" @default.
• W2010052871 creator A5009849396 @default.
• W2010052871 date "2009-06-01" @default.
• W2010052871 modified "2023-09-25" @default.
• W2010052871 title "Transferability of polarizable models for ion-water electrostatic interaction" @default.
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• W2010052871 doi "https://doi.org/10.1088/1742-6596/177/1/012004" @default.
• W2010052871 hasPublicationYear "2009" @default.
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