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dc.contributor.authorPérez-Torralba, Marta-
dc.contributor.authorGarcía, M. Ángeles-
dc.contributor.authorLópez, Concepción-
dc.contributor.authorTorralba, M. Carmen-
dc.contributor.authorTorres, M. Rosario-
dc.contributor.authorClaramunt, Rosa M.-
dc.date.accessioned2014-09-11T10:06:14Z-
dc.date.available2014-09-11T10:06:14Z-
dc.date.issued2014-
dc.identifierdoi: 10.1021/cg500442k-
dc.identifierissn: 1528-7483-
dc.identifiere-issn: 1528-7505-
dc.identifier.citationCrystal Growth and Design 14: 3499- 3509 (2014)-
dc.identifier.urihttp://hdl.handle.net/10261/102009-
dc.description.abstractThe structures of five fluorinated benzimidazoles and one intermediate (an open double amide) have been determined by X-ray crystallography. In the analysis of these heterocycles, particular attention has been paid to N-H⋯H hydrogen bonds and to fluorine-fluorine intermolecular contacts. Thus, one of the shortest F⋯F distances ever reported, 2.596(3) Å, has been observed in 4,5,6,7-tetrafluoro-1H-benzimidazole-2(3H)-one. The 13C, 15N, and 19F solid-state NMR data for all benzimidazoles are also given.-
dc.publisherAmerican Chemical Society-
dc.rightsclosedAccess-
dc.titleStructural investigation of weak intermolecular interactions (Hydrogen and Halogen Bonds) in fluorine-substituted benzimidazoles-
dc.typeartículo-
dc.identifier.doi10.1021/cg500442k-
dc.date.updated2014-09-11T10:06:14Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
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