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dc.contributor.authorHsu, Kuo-Hsiangen_US
dc.contributor.authorHuang, Yu-Hsuanen_US
dc.contributor.authorLee, Yuan-Pernen_US
dc.contributor.authorHuang, Mengen_US
dc.contributor.authorMiller, Terry A.en_US
dc.contributor.authorMcCoy, Anne B.en_US
dc.date.accessioned2017-04-21T06:56:17Z-
dc.date.available2017-04-21T06:56:17Z-
dc.date.issued2016-07-14en_US
dc.identifier.issn1089-5639en_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.jpca.5b12334en_US
dc.identifier.urihttp://hdl.handle.net/11536/134023-
dc.description.abstractWith a step-scan Fourier-transform spectrometer we recorded temporally resolved infrared absorption spectra of CH3OO radicals that were produced upon irradiation of CH3COCH3 and O-2 at 193 nm in a flowing mixture. At a resolution of 0.15 cm(-1), the rotational structure of the nu(2) band of CH3OO near 2954.4 cm(-1) is partially resolved and shows an unexpectedly broadened, and somewhat distorted, Q-branch. A 4D model Hamiltonian, consisting of three CH stretches and the methyl torsion, was developed to explore the origins of this broadening. The vibrational progressions predicted by the model Hamiltonian and the rotational contours of the nu(2) band, based on experimental ground-state rotational parameters and their values scaled by their calculated ratios for the upper state, produced simulations in satisfactory agreement with the observed spectrum. These results provide new inSight into the vibrational couplings in CH3OO.en_US
dc.language.isoen_USen_US
dc.titleManifestations of Torsion-CH Stretch Coupling in the Infrared Spectrum of CH3OOen_US
dc.identifier.doi10.1021/acs.jpca.5b12334en_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY Aen_US
dc.citation.volume120en_US
dc.citation.issue27en_US
dc.citation.spage4827en_US
dc.citation.epage4837en_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:000379988900026en_US
Appears in Collections:Articles