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Solute-solvent intermolecular vibronic coupling as manifested by the molecular near-field effect in resonance hyper-Raman scattering

dc.citation.epageen_US
dc.citation.issue3en_US
dc.citation.volume134en_US
dc.citation.woscount4
dc.contributor.authorShimada, Rintaroen_US
dc.contributor.authorHamaguchi, Hiro-oen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.date.accessioned2014-12-08T15:37:37Z
dc.date.available2014-12-08T15:37:37Z
dc.date.issued2011-01-21en_US
dc.description.abstractVibronic coupling within the excited electronic manifold of the solute all-trans-beta-carotene through the vibrational motions of the solvent cyclohexane is shown to manifest as the "molecular near-field effect," in which the solvent hyper-Raman bands are subject to marked intensity enhancements under the presence of all-trans-beta-carotene. The resonance hyper-Raman excitation profiles of the enhanced solvent bands exhibit similar peaks to those of the solute bands in the wavenumber region of 21 700-25 000 cm(-1) (10 850-12 500 cm(-1) in the hyper-Raman exciting wavenumber), where the solute all-trans-beta-carotene shows a strong absorption assigned to the 1A(g) -> 1B(u) transition. This fact indicates that the solvent hyper-Raman bands gain their intensities through resonances with the electronic states of the solute. The observed excitation profiles are quantitatively analyzed and are successfully accounted for by an extended vibronic theory of resonance hyper-Raman scattering that incorporates the vibronic coupling within the excited electronic manifold of all-trans-beta-carotene through the vibrational motions of cyclohexane. It is shown that the major resonance arises from the B-term (vibronic) coupling between the first excited vibrational level (v = 1) of the 1B(u) state and the ground vibrational level (v = 0) of a nearby A(g) state through ungerade vibrational modes of both the solute and the solvent molecules. The inversion symmetry of the solute all-trans-beta-carotene is preserved, suggesting the weak perturbative nature of the solute-solvent interaction in the molecular near-field effect. The present study introduces a new concept, " intermolecular vibronic coupling," which may provide an experimentally accessible/theoretically tractable model for understanding weak solute-solvent interactions in liquid. (C) 2011 American Institute of Physics. [doi:10.1063/1.3512923]en_US
dc.identifier.doi10.1063/1.3512923en_US
dc.identifier.issn0021-9606en_US
dc.identifier.journalJOURNAL OF CHEMICAL PHYSICSen_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.3512923en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/25871
dc.identifier.wosnumberWOS:000286472200057
dc.language.isoen_USen_US
dc.titleSolute-solvent intermolecular vibronic coupling as manifested by the molecular near-field effect in resonance hyper-Raman scatteringen_US
dc.typeArticleen_US

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