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dc.contributor.authorMerer, Anthony J.en_US
dc.contributor.authorYamakita, Namien_US
dc.contributor.authorTsuchiya, Sojien_US
dc.contributor.authorSteeves, Adam H.en_US
dc.contributor.authorBechtel, Hans A.en_US
dc.contributor.authorField, Robert W.en_US
dc.date.accessioned2014-12-08T15:11:03Z-
dc.date.available2014-12-08T15:11:03Z-
dc.date.issued2008-08-07en_US
dc.identifier.issn0021-9606en_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.2939246en_US
dc.identifier.urihttp://hdl.handle.net/11536/8473-
dc.description.abstractRotational analyses have been carried out for the overtones of the nu(4) (torsion) and nu(6) (in-plane cis-bend) vibrations of the (A) over tilde (1)A(u) state of C(2)H(2). The v(4)+v(6)=2 vibrational polyad was observed in high-sensitivity one-photon laser-induced fluorescence spectra and the v(4)+v(6)=3 polyad was observed in IR-UV double resonance spectra via the ground state nu(3) (Sigma(+)(u)) and nu(3)+nu(4) (Pi(u)) vibrational levels. The structures of these polyads are dominated by the effects of vibrational angular momentum: Vibrational levels of different symmetry interact via strong a-and b-axis Coriolis coupling, while levels of the same symmetry interact via Darling-Dennison resonance, where the interaction parameter has the exceptionally large value K(4466)=-51.68 cm(-1). The K-structures of the polyads bear almost no resemblance to the normal asymmetric top patterns, and many local avoided crossings occur between close-lying levels with nominal K-values differing by one or more units. Least squares analysis shows that the coupling parameters change only slightly with vibrational excitation, which has allowed successful predictions of the structures of the higher polyads: A number of weak bands from the v(4)+v(6)=4 and 5 polyads have been identified unambiguously. The state discovered by Scherer [J. Chem. Phys. 85, 6315 (1986)], which appears to interact with the K=1 levels of the 3(3) vibrational state at low J, is identified as the second highest of the five K=1 members of the v(4)+v(6)=4 polyad. After allowing for the Darling-Dennison resonance, the zero-order bending structure can be represented by omega(4)=764.71, omega(6)=772.50, x(44)=0.19, x(66)=-4.23, and x(46)=11.39 cm(-1). The parameters x(46) and K(4466) are both sums of contributions from the vibrational angular momentum and from the anharmonic force field. For x(46) these contributions are 14.12 and -2.73 cm(-1), respectively, while the corresponding values for K(4466) are -28.24 and -23.44 cm(-1). It is remarkable how severely the coupling of nu(4) and nu(6) distorts the overtone polyads, and also how in this case the effects of vibrational angular momentum outweigh those of anharmonicity in causing the distortion. (C) 2008 American Institute of Physics.en_US
dc.language.isoen_USen_US
dc.titleDarling-Dennison resonance and Coriolis coupling in the bending overtones of the (A)over-tilde (1)A(u) state of acetylene, C(2)H(2)en_US
dc.typeArticleen_US
dc.identifier.doi10.1063/1.2939246en_US
dc.identifier.journalJOURNAL OF CHEMICAL PHYSICSen_US
dc.citation.volume129en_US
dc.citation.issue5en_US
dc.citation.epageen_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.identifier.wosnumberWOS:000258336100016-
dc.citation.woscount17-
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