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dc.contributor.authorAnmol Kumar-
dc.contributor.authorGadre, S R-
dc.contributor.authorNeetha Mohan-
dc.contributor.authorSuresh, C H-
dc.date.accessioned2014-02-18T10:06:35Z-
dc.date.available2014-02-18T10:06:35Z-
dc.date.issued2014-
dc.identifier.citationJournal of Physical Chemistry A 118(2):526–532,16 Jan 2014en_US
dc.identifier.issn1089-5639-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/1188-
dc.description.abstractA clear-cut definition of lone pairs has been offered in terms of characteristics of minima in molecular electrostatic potential (MESP). The largest eigenvalue and corresponding eigenvector of the Hessian at the minima are shown to distinguish lone pair regions from the other types of electron localization (such as π bonds). A comparative study of lone pairs as depicted by various other scalar fields such as the Laplacian of electron density and electron localization function is made. Further, an attempt has been made to generalize the definition of lone pairs to the case of cations.en_US
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.subjectLone Pairsen_US
dc.subjectAtoms in molecules (AIM)en_US
dc.subjectVSEPRen_US
dc.titleLone Pairs: An Electrostatic viewpointen_US
dc.typeArticleen_US
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