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dc.creatorCormanich, Rodrigo A.-
dc.creatorFreitas, Matheus P.-
dc.creatorTormena, Cláudio F.-
dc.creatorRittner, Roberto-
dc.date.accessioned2020-07-12T23:09:11Z-
dc.date.available2020-07-12T23:09:11Z-
dc.date.issued2012-03-
dc.identifier.citationCORMANICH, R. A. F...HO intramolecular hydrogen bond forming five-membered rings hardly appears in monocyclic organofluorine compounds. RSC Advances, [S.l.], v. 2, n. 10, p. 4169-4174, Mar. 2012.pt_BR
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2012/RA/c2ra00039c#!divAbstractpt_BR
dc.identifier.urihttp://repositorio.ufla.br/jspui/handle/1/41820-
dc.description.abstractThis paper emphasizes that fluorine atoms in organic molecules need special geometric requirements to experience intramolecular hydrogen bonds (H-bonds). Calculations at the B3LYP/aug-cc-pVDZ theoretical level and using the quantum theory of atoms in molecules applied over a series of monocyclic compounds, which have similar C[double bond, length as m-dash]C(F)–C(OH)[double bond, length as m-dash]C fragments, predict that the F⋯HO intramolecular H-bond does not exist when forming five-membered rings. Indeed, it is shown that the geometric restrictions imposed by the rigid rings are the main reasons in preventing fluorine participating in such a F⋯HO intramolecular H-bond.pt_BR
dc.languageen_USpt_BR
dc.publisherRoyal Society of Chemistry (RSC)pt_BR
dc.rightsrestrictAccesspt_BR
dc.sourceRSC Advancespt_BR
dc.subjectFluorinept_BR
dc.subjectH-bondspt_BR
dc.subjectMonocyclic compoundspt_BR
dc.titleF...HO intramolecular hydrogen bond forming five-membered rings hardly appears in monocyclic organofluorine compoundspt_BR
dc.typeArtigopt_BR
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