1981
DOI: 10.1016/0009-2614(81)85228-1
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The electric quadrupole moments of benzene and hexafluorobenzene

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Cited by 246 publications
(136 citation statements)
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“…Because the lϭ0 partial wave occurs in the A 1g representation, one might ordinarily expect that the cross section vanish at zero energy for all other representations. 29 However, benzene has a substantial quadrupole moment, 30 and the resulting 1/r 3 potential will give rise to a nonzero scattering cross section at zero energy for lϾ0. [31][32][33] Indeed, using the measured quadrupole moment, 30 one can estimate the magnitude of the quadrupole-induced scattering within the Born approximation 32 as about 13ϫ10 Ϫ16 cm 2 , a value which appears roughly consistent with the summed results of Gianturco and Lucchese.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Because the lϭ0 partial wave occurs in the A 1g representation, one might ordinarily expect that the cross section vanish at zero energy for all other representations. 29 However, benzene has a substantial quadrupole moment, 30 and the resulting 1/r 3 potential will give rise to a nonzero scattering cross section at zero energy for lϾ0. [31][32][33] Indeed, using the measured quadrupole moment, 30 one can estimate the magnitude of the quadrupole-induced scattering within the Born approximation 32 as about 13ϫ10 Ϫ16 cm 2 , a value which appears roughly consistent with the summed results of Gianturco and Lucchese.…”
Section: Discussionmentioning
confidence: 99%
“…29 However, benzene has a substantial quadrupole moment, 30 and the resulting 1/r 3 potential will give rise to a nonzero scattering cross section at zero energy for lϾ0. [31][32][33] Indeed, using the measured quadrupole moment, 30 one can estimate the magnitude of the quadrupole-induced scattering within the Born approximation 32 as about 13ϫ10 Ϫ16 cm 2 , a value which appears roughly consistent with the summed results of Gianturco and Lucchese. However, it is not possible to say from the data presented in their paper whether the results of Gianturco and Lucchese are consistent with the quadrupole mechanism, which also predicts isotropic scattering and an energy-independent cross section.…”
Section: Discussionmentioning
confidence: 99%
“…However, as was shown before, the 19 F-labeling of the aromatic system in RNA nucleobases can have two opposing effects. The base pairing stability is decreased (Broom et al 1979) whereas the base stacking is increased (Battaglia et al 1981). These two opposing effects can compensate each other so that the overall stability of the RNA is not impaired.…”
Section: Local Stabilitymentioning
confidence: 99%
“…[30][31][32] To analyse the interaction type in detail we performed BEDA and also CDA. The BEDA data are provided in analysis is needed to get more precise result.…”
Section: Nature Of Interactionmentioning
confidence: 99%