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dc.contributor.authorLo, Rabindranath
dc.contributor.authorManna, Debashree
dc.contributor.authorMiriyala, Vijay Madhav
dc.contributor.authorNachtigallová, Dana
dc.contributor.authorHobza, Pavel
dc.date.accessioned2024-03-27T11:51:15Z
dc.date.available2024-03-27T11:51:15Z
dc.date.issued2023
dc.identifier.citationPhysical Chemistry Chemical Physics. 2023, vol. 25, issue 38, p. 25961-25964.cs
dc.identifier.issn1463-9076
dc.identifier.issn1463-9084
dc.identifier.urihttp://hdl.handle.net/10084/152477
dc.description.abstractIn general, the stability of neutral complexes with dative bonds increases as the polarity of the solvent increases. This is based on the fact that the dipole moment of the complex increases as the charge transferred from the donor to the acceptor increases. As a result, the solvation energy of the complex becomes greater than that of subsystems, causing an increase in the stabilization energy with increasing solvent polarity. Our research confirms this assumption, but only when the charge transfer is sufficiently large. If it is below a certain threshold, the increase in the complex's dipole moment is insufficient to result in a higher solvation energy than subsystems. Thus, the magnitude of the charge transfer in the Lewis electron-pair system determines the stability trends of dative bonds with varying solvent polarity. We used molecular dynamics (MD) simulations based on an explicit solvent model, which is considered more reliable, to verify the results obtained with a continuous solvent model.cs
dc.language.isoencs
dc.publisherRoyal Society of Chemistrycs
dc.relation.ispartofseriesPhysical Chemistry Chemical Physicscs
dc.relation.urihttps://doi.org/10.1039/d3cp03445ccs
dc.rightsThis journal is © the Owner Societies 2023cs
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/cs
dc.titleTrends in the stability of covalent dative bonds with variable solvent polarity depend on the charge transfer in the Lewis electron-pair systemcs
dc.typearticlecs
dc.identifier.doi10.1039/d3cp03445c
dc.rights.accessopenAccesscs
dc.type.versionpublishedVersioncs
dc.type.statusPeer-reviewedcs
dc.description.sourceWeb of Sciencecs
dc.description.volume25cs
dc.description.issue38cs
dc.description.lastpage25964cs
dc.description.firstpage25961cs
dc.identifier.wos001067478800001


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