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dc.contributor.authorKaramertzanis, P.G.*
dc.contributor.authorDay, G.M.*
dc.contributor.authorWelch, G.W.A.*
dc.contributor.authorKendrick, John*
dc.contributor.authorLeusen, Frank J.J.*
dc.contributor.authorNeumann, M.A.*
dc.contributor.authorPrice, S.L.*
dc.date.accessioned2011-01-20T15:28:31Z
dc.date.available2011-01-20T15:28:31Z
dc.date.issued2011-01-20T15:28:31Z
dc.identifier.citationKaramertzanis, P. G., Day, G. M., Welch, G. W. A., Kendrick, J., Leusen, F. J. J., Neumann, M. A. and Price, S. L. (2008). Modeling the interplay of inter- and intramolecular hydrogen bonding in conformational polymorphs. Journal of Chemical Physics, Vol. 128, 244708, doi:10.1063/1.2937446 (17p.)en
dc.identifier.urihttp://hdl.handle.net/10454/4734
dc.descriptionnoen
dc.description.abstractThe predicted stability differences of the conformational polymorphs of oxalyl dihydrazide and ortho-acetamidobenzamide are unrealistically large when the modeling of intermolecular energies is solely based on the isolated-molecule charge density, neglecting charge density polarization. Ab initio calculated crystal electron densities showed qualitative differences depending on the spatial arrangement of molecules in the lattice with the greatest variations observed for polymorphs that differ in the extent of inter- and intramolecular hydrogen bonding. We show that accounting for induction dramatically alters the calculated stability order of the polymorphs and reduces their predicted stability differences to be in better agreement with experiment. Given the challenges in modeling conformational polymorphs with marked differences in hydrogen bonding geometries, we performed an extensive periodic density functional study with a range of exchange-correlation functionals using both atomic and plane wave basis sets. Although such electronic structure methods model the electrostatic and polarization contributions well, the underestimation of dispersion interactions by current exchange-correlation functionals limits their applicability. The use of an empirical dispersion-corrected density functional method consistently reduces the structural deviations between the experimental and energy minimized crystal structures and achieves plausible stability differences. Thus, we have established which types of models may give worthwhile relative energies for crystal structures and other condensed phases of flexible molecules with intra- and intermolecular hydrogen bonding capabilities, advancing the possibility of simulation studies on polymorphic pharmaceuticals.en
dc.language.isoenen
dc.publisherAmerican Institute of Physicsen
dc.relation.isreferencedbyhttp://dx.doi.org/10.1063/1.2937446en
dc.subjectCrystal Structureen
dc.subjectPolymorphismen
dc.subjectStabilityen
dc.titleModeling the interplay of inter- and intramolecular hydrogen bonding in conformational polymorphs.en
dc.status.refereedYesen
dc.typeArticleen
dc.identifier.JournalTitleJ. Chem. Phys. 128, 244708 (2008)en
dc.type.versionNo full-text available in the repositoryen


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