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A possible nonpolar solvation mechanism at an intermediate time scale: the solvent-cage expansion

dc.citation.epage388en_US
dc.citation.issue5-6en_US
dc.citation.spage381en_US
dc.citation.volume324en_US
dc.citation.woscount3
dc.contributor.authorChang, SLen_US
dc.contributor.authorWu, TMen_US
dc.contributor.department物理研究所zh_TW
dc.contributor.departmentInstitute of Physicsen_US
dc.date.accessioned2014-12-08T15:45:03Z
dc.date.available2014-12-08T15:45:03Z
dc.date.issued2000-07-14en_US
dc.description.abstractThrough studying the so-called 'epsilon' nonpolar solvation model, we propose that the expansion of the solvent cage, which is composed of the solvents at the vicinity of the first maximum of the solute-solvent radial distribution function, might be a possible solvation mechanism at a time scale between inertial motions and structural relaxation. The expansion is triggered by the strong repulsion between the solute and its neighboring solvents, originally inside the cage. This intermediate mechanism is found to be the cause for the bump following the ultrafast decay in the solvation time correlation functions of the 'epsilon' model at low densities. (C) 2000 Elsevier Science B.V. All rights reserved.en_US
dc.identifier.issn0009-2614en_US
dc.identifier.journalCHEMICAL PHYSICS LETTERSen_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/30390
dc.identifier.wosnumberWOS:000088175900010
dc.language.isoen_USen_US
dc.titleA possible nonpolar solvation mechanism at an intermediate time scale: the solvent-cage expansionen_US
dc.typeArticleen_US

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