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On the weakly C–H⋯π hydrogen bonded complexes of sevoflurane and benzene

dc.contributor.authorDom, Johan J. J.
dc.contributor.authorvan der Veken, Benjamin J.
dc.contributor.authorMichielsen, Bart
dc.contributor.authorJacobs, Sam
dc.contributor.authorXue, Zhifeng
dc.contributor.authorHesse, Susanne
dc.contributor.authorLoritz, Hans-Martin
dc.contributor.authorSuhm, Martin A.
dc.contributor.authorHerrebout, Wouter A.
dc.date.accessioned2013-03-15T11:41:41Z
dc.date.available2013-03-15T11:41:41Z
dc.date.issued2011
dc.identifier.citationDom, Johan J. J.; van der Veken, Benjamin J.; Michielsen, Bart; Jacobs, Sam; Xue, Zhifeng; Hesse, Susanne; Loritz, Hans-Martin; Suhm, Martin A.; Herrebout, Wouter A. (2011): On the weakly C–H⋯π hydrogen bonded complexes of sevoflurane and benzene
dc.relation.ISSN1463-9084
dc.identifier.urihttp://resolver.sub.uni-goettingen.de/purl?gs-1/8712
dc.description.abstractA vibrational assignment of the anaesthetic sevoflurane, (CF3)2CHOCH2F, is proposed and its interaction with the aromatic model compound benzene is studied using vibrational spectroscopy of supersonic jet expansions and of cryosolutions in liquid xenon. Ab initio calculations, at the MP2/cc-pVDZ and MP2/aug-cc-pVDZ levels, predict two isomers for the 1 : 1 complex, one in which the near-cis, gauche conformer of sevoflurane is hydrogen bonded through its isopropylhydrogen atom, the other in which the same conformer is bonded through a bifurcated hydrogen bond with the fluoromethyl hydrogen atoms. From the experiments it is shown that the two isomers are formed, however with a strong population dominance of the isopropyl-bonded species, both in the jet and liquid phase spectra. The experimental complexation enthalpy in liquid xenon, DHo(LXe), of this species equals 10.9(2) kJ mol 1, as derived from the temperature dependent behaviour of the cryosolution spectra. Theoretical complexation enthalpies in liquid xenon were obtained by combining the complete basis set extrapolated complexation energies at the MP2/aug-cc-pVXZ (X = D,T) level with corrections derived from statistical thermodynamics and Monte Carlo Free Energy Perturbation calculations, resulting in a complexation enthalpy of 11.2(3) kJ mol 1 for the isopropyl-bonded complex, in very good agreement with the experimental value, and of 11.4(4) kJ mol 1, for the fluoromethyl-bonded complex. The Monte Carlo calculations show that the solvation entropy of the isopropyl-bonded species is considerably higher than that of the fluoromethyl-bonded complex, which assists in explaining its dominance in the liquid phase spectra.
dc.language.isoeng
dc.rightsopenAccess
dc.subjectmembrane proteins; anaesthetic sevoflurane; vibrational spectroscopy; liquid phase spectra
dc.titleOn the weakly C–H⋯π hydrogen bonded complexes of sevoflurane and benzene
dc.typejournalArticle
dc.identifier.doi10.1039/c1cp20693a
dc.type.versionpublishedVersion
dc.identifier.fs590192
dc.relation.pISSN1463-9076
dc.bibliographicCitation.volume13
dc.bibliographicCitation.issue31
dc.bibliographicCitation.firstPage14142
dc.bibliographicCitation.lastPage14152
dc.type.subtypejournalArticle
dc.notesThis publication is with permission of the rights owner freely accessible due to an Alliance licence and a national licence (funded by the DFG, German Research Foundation) respectively.
dc.description.statuspeerReviewed
dc.bibliographicCitation.journalPhysical Chemistry Chemical Physics


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