dc.creatorCormanich, Rodrigo A.
dc.creatorMoreira, Marilua A.
dc.creatorFreitas, Matheus P.
dc.creatorRamalho, Teodorico C.
dc.creatorAnconi, Cléber P. A.
dc.creatorRittner, Roberto
dc.creatorContreras, Ruben Horacio
dc.creatorTormena, Cláudio F.
dc.date.accessioned2018-08-22T18:58:47Z
dc.date.accessioned2018-11-06T13:57:49Z
dc.date.available2018-08-22T18:58:47Z
dc.date.available2018-11-06T13:57:49Z
dc.date.created2018-08-22T18:58:47Z
dc.date.issued2011-11
dc.identifierCormanich, Rodrigo A.; Moreira, Marilua A.; Freitas, Matheus P.; Ramalho, Teodorico C.; Anconi, Cléber P. A.; et al.; 1hJFH coupling in 2-fluorophenol revisited: Is intramolecular hydrogen bond responsible for this long-range coupling?; John Wiley & Sons Ltd; Magnetic Resonance in Chemistry; 49; 12; 11-2011; 763-767
dc.identifier0749-1581
dc.identifierhttp://hdl.handle.net/11336/56670
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1881170
dc.description.abstractThe present study shows that a hydrogen bond between the OH group and the fluorine atom is not involved in the 1hJFH spin-spin coupling transmission either for 4-bromo-2-fluorophenol or 2-fluorophenol. In fact, according to a quantum theory of atoms in molecules analysis, no bond critical point is found between O-H and F moieties. The nature of the transmission mechanism of the Fermi contact term of the 1hJ FH spin-spin coupling is studied by analyzing canonical molecular orbitals (see J. Phys. Chem. A 2010, 114, 1044), and it is observed that virtual orbitals play only a quite minor role in its transmission. This is typical of a Fermi contact term transmitted mainly through exchange interactions owing to the overlap of proximate electronic clouds; therefore, it is suggested to identify them as nTSJFH coupling where n stands for the number of formal bonds separating the coupling nuclei. In the cases studied in this work is n = 4. Results presented in this work could provide an interesting rationalization for different experimental signs known in the current literature for proximate JFH couplings. © 2011 John Wiley & Sons, Ltd.
dc.languageeng
dc.publisherJohn Wiley & Sons Ltd
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/mrc.2838
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subject2-FLUOROPHENOL
dc.subjectCOUPLING CONSTANT
dc.subjectFCCP-CMO
dc.subjectINTRAMOLECULAR H-BONDING
dc.subjectQTAIM
dc.title1hJFH coupling in 2-fluorophenol revisited: Is intramolecular hydrogen bond responsible for this long-range coupling?
dc.typeArtículos de revistas
dc.typeArtículos de revistas
dc.typeArtículos de revistas


Este ítem pertenece a la siguiente institución