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Infrared absorption of gaseous ClCS detected with time-resolved Fourier-transform spectroscopy

dc.citation.epageen_US
dc.citation.issue17en_US
dc.citation.volume126en_US
dc.citation.woscount6
dc.contributor.authorChu, Li-Kangen_US
dc.contributor.authorHan, Hui-Lingen_US
dc.contributor.authorLee, Yuan-Pernen_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.accessioned2014-12-08T15:14:04Z
dc.date.available2014-12-08T15:14:04Z
dc.date.issued2007-05-07en_US
dc.description.abstractA transient infrared absorption spectrum of gaseous ClCS was detected with a step-scan Fourier-transform spectrometer coupled with a multipass absorption cell. ClCS was produced upon irradiating a flowing mixture of Cl2CS and N-2 or CO2 with a KrF excimer laser at 248 nm. A transient band in the region of 1160-1220 cm(-1), which diminished on prolonged reaction, is assigned to the C-S stretching (nu(1)) mode of ClCS. Calculations with density-functional theory (B3P86 and B3LYP/aug-cc-pVTZ) predict the geometry, vibrational wave numbers, and rotational parameters of ClCS. The rotational contour of the spectrum of ClCS simulated based on predicted rotational parameters agrees satisfactorily with experimental observation; from spectral simulation, the band origin is determined to be at 1194.4 cm(-1). Reaction kinetics involving ClCS, CS, and CS2 are discussed. (C) 2007 American Institute of Physics.en_US
dc.identifier.doi10.1063/1.2730501en_US
dc.identifier.issn0021-9606en_US
dc.identifier.journalJOURNAL OF CHEMICAL PHYSICSen_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.2730501en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/10813
dc.identifier.wosnumberWOS:000246284800018
dc.language.isoen_USen_US
dc.titleInfrared absorption of gaseous ClCS detected with time-resolved Fourier-transform spectroscopyen_US
dc.typeArticleen_US

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