dc.creator | Cormanich, Rodrigo A. | |
dc.creator | Moreira, Marilua A. | |
dc.creator | Freitas, Matheus P. | |
dc.creator | Ramalho, Teodorico C. | |
dc.creator | Anconi, Cléber P. A. | |
dc.creator | Rittner, Roberto | |
dc.creator | Contreras, Ruben Horacio | |
dc.creator | Tormena, Cláudio F. | |
dc.date.accessioned | 2018-08-22T18:58:47Z | |
dc.date.accessioned | 2018-11-06T13:57:49Z | |
dc.date.available | 2018-08-22T18:58:47Z | |
dc.date.available | 2018-11-06T13:57:49Z | |
dc.date.created | 2018-08-22T18:58:47Z | |
dc.date.issued | 2011-11 | |
dc.identifier | Cormanich, 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.identifier | 0749-1581 | |
dc.identifier | http://hdl.handle.net/11336/56670 | |
dc.identifier | CONICET Digital | |
dc.identifier | CONICET | |
dc.identifier.uri | http://repositorioslatinoamericanos.uchile.cl/handle/2250/1881170 | |
dc.description.abstract | The 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.language | eng | |
dc.publisher | John Wiley & Sons Ltd | |
dc.relation | info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1002/mrc.2838 | |
dc.rights | https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ | |
dc.rights | info:eu-repo/semantics/restrictedAccess | |
dc.subject | 2-FLUOROPHENOL | |
dc.subject | COUPLING CONSTANT | |
dc.subject | FCCP-CMO | |
dc.subject | INTRAMOLECULAR H-BONDING | |
dc.subject | QTAIM | |
dc.title | 1hJFH coupling in 2-fluorophenol revisited: Is intramolecular hydrogen bond responsible for this long-range coupling? | |
dc.type | Artículos de revistas | |
dc.type | Artículos de revistas | |
dc.type | Artículos de revistas | |