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Journal ArticleDOI

What can x-ray scattering tell us about the radial distribution functions of water?

Jon M. Sorenson, +3 more
- 09 Nov 2000 - 
- Vol. 113, Iss: 20, pp 9149-9161
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TLDR
In this paper, an analysis of the Advanced Light Source (ALS) x-ray scattering experiment on pure liquid water at ambient temperature and pressure described in the preceding article is presented.
Abstract
We present an analysis of the Advanced Light Source (ALS) x-ray scattering experiment on pure liquid water at ambient temperature and pressure described in the preceding article. The present study discusses the extraction of radial distribution functions from the x-ray scattering of molecular fluids. It is proposed that the atomic scattering factors used to model water be modified to include the changes in the intramolecular electron distribution caused by chemical bonding effects. Based on this analysis we present a gOO(r) for water consistent with our recent experimental data gathered at the ALS, which differs in some aspects from the gOO(r) reported by other x-ray and neutron scattering experiments. Our gOO(r) exhibits a taller and sharper first peak, and systematic shifts in all peak positions to smaller r. Based on experimental uncertainties, we discuss what features of gOO(r) should be reproduced by classical simulations of nonpolarizable and polarizable water models, as well as ab initio simulations of water, at ambient conditions. We directly compare many water models and simulations to the present data, and discuss possible improvements in both classical and ab initio simulation approaches in the future.

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Citations
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Journal ArticleDOI

Potential energy functions for atomic-level simulations of water and organic and biomolecular systems.

TL;DR: An overview of potential energy functions that are used in atomic-level statistical mechanics and molecular dynamics simulations of water and of organic and biomolecular systems can be found in this paper.
Journal ArticleDOI

Flexible simple point-charge water model with improved liquid-state properties

TL;DR: A new flexible simple point-charge water model was derived by optimizing bulk diffusion and dielectric constants to the experimental values via the equilibrium bond length and angle and extensive comparisons of thermodynamic, structural, and kinetic properties indicate that the new model is much improved over the standard SPC model and its overall performance is comparable to or even better than the extended SPC models.
Journal ArticleDOI

A modified TIP3P water potential for simulation with Ewald summation.

TL;DR: Several similar models are considered with the additional constraint of trying to match the performance of the optimized potentials for liquid simulation atom force field to that obtained when using the simulation conditions under which it was originally designed, but no model was entirely satisfactory in reproducing the relative difference in free energies of hydration between the model compounds, phenol and benzene.
Journal ArticleDOI

A reappraisal of what we have learnt during three decades of computer simulations on water

TL;DR: The purpose is to appraise what have been accomplished during all these years of model potentials publication and testing and what deserves to be improved and to give some guidance for future investigations.
Journal ArticleDOI

A simple polarizable model of water based on classical Drude oscillators

TL;DR: In this article, a simple polarizable water model is developed and optimized for molecular dynamics simulations of the liquid phase under ambient conditions, where the permanent charge distribution of the water molecule is represented by three point charges: two hydrogen sites and one additional M site positioned along the HOH bisector.
References
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Journal ArticleDOI

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Journal ArticleDOI

Comparison of simple potential functions for simulating liquid water

TL;DR: In this article, the authors compared the Bernal Fowler (BF), SPC, ST2, TIPS2, TIP3P, and TIP4P potential functions for liquid water in the NPT ensemble at 25°C and 1 atm.
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