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• W2091002009 abstract "The existence of accurately measured oxygen pair-correlation functions for liquid water suggests a natural form of linear perturbation theory for that substance. The unperturbed potential involves isotropically interacting molecules, and reproduces the measured oxygen-pair short-range order. Monte Carlo simulations in this theoretical context have been carried out for the unperturbed system and for the fully coupled system in the liquid state at 25 ifmmode^circelsetextdegreefi{}C. Inherent structures (potential-energy minima) have been generated and examined in both of these cases; they demonstrate that the directionality intrinsic to hydrogen bonding plays an important role in structurally stabilizing short-range order at the pair and higher-order correlation levels." @default.
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• W2091002009 date "1993-04-01" @default.
• W2091002009 modified "2023-10-18" @default.
• W2091002009 title "Perturbational view of inherent structures in water" @default.
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• W2091002009 doi "https://doi.org/10.1103/physreve.47.2484" @default.
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