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dc.contributor.authorCamacho, Cristopheren_US
dc.contributor.authorCheng, Chi-Wenen_US
dc.contributor.authorWitek, Henryk A.en_US
dc.contributor.authorLee, Yuan-Pernen_US
dc.date.accessioned2014-12-08T15:48:05Z-
dc.date.available2014-12-08T15:48:05Z-
dc.date.issued2010-10-21en_US
dc.identifier.issn1089-5639en_US
dc.identifier.urihttp://dx.doi.org/10.1021/jp105664ken_US
dc.identifier.urihttp://hdl.handle.net/11536/32063-
dc.description.abstractAccurate multireference configuration interaction and time-dependent density functional calculations have been performed to interpret the experimental UV-vis spectrum of the CS(2)/Cl complex in the spectral region 320-550 nm. The molecular structure of the complex responsible for the previously observed UV-vis spectrum is recognized as ClSCS, not CICS(2). Two low-lying excited states of ClSCS, responsible for its optical absorption, have been identified and analyzed. Optical excitation of ClSCS leads to the excitation-specific bond elongation that may lead to photofragmentation of the molecule. In addition, experimental conditions for verifying the presence of ClCS(2) are identified and detailed characterization of its optically active excited states with possible photofragmentation pathways is given.en_US
dc.language.isoen_USen_US
dc.titleTheoretical Interpretation of the UV-vis Spectrum of the CS(2)/Cl Complex in the Spectral Region 320-550 nmen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/jp105664ken_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY Aen_US
dc.citation.volume114en_US
dc.citation.issue41en_US
dc.citation.spage11008en_US
dc.citation.epage11016en_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
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