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dc.contributor.authorLiu, CPen_US
dc.contributor.authorReid, SAen_US
dc.contributor.authorLee, YPen_US
dc.date.accessioned2014-12-08T15:19:30Z-
dc.date.available2014-12-08T15:19:30Z-
dc.date.issued2005-03-22en_US
dc.identifier.issn0021-9606en_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.1867333en_US
dc.identifier.urihttp://hdl.handle.net/11536/13888-
dc.description.abstractWe report results of two-color resonant four-wave mixing experiments on highly predissociated levels of the methylthio (or thiomethoxy) radical CH3S in its first excited electronic state A (2)A(1). Following photolysis of jet-cooled dimethyl disulfide at 248 nm, the spectra were measured with a hole-burning scheme in which the probe laser excited specific rotational transitions in band 3(3). The spectral simplification afforded by the two-color method allows accurate determination of line positions and homogeneous linewidths, which are reported for the C-S stretching states 3(v)(v=3-7) and combination states 1(1)3(v)(v=0-2), 2(1)3(v)(v=3-6), and 1(1)2(1)3(v)(v=0,1) involving the symmetric CH3 stretching (nu(1)) mode and the CH3 umbrella (nu(2)) mode. The spectra show pronounced mode specificity, as the homogeneous linewidth of levels with similar energies varies up to two orders of magnitude; nu(3) is clearly a promoting mode for dissociation. Derived vibrational wave numbers omega(1)('), omega(2)('), and omega(3)(') of the A state agree satisfactorily with ab initio predictions.en_US
dc.language.isoen_USen_US
dc.titleTwo-color resonant four-wave mixing spectroscopy of highly predissociated levels in the (A)over-tilde(2)A(1) state of CH3Sen_US
dc.typeArticleen_US
dc.identifier.doi10.1063/1.1867333en_US
dc.identifier.journalJOURNAL OF CHEMICAL PHYSICSen_US
dc.citation.volume122en_US
dc.citation.issue12en_US
dc.citation.epageen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000228287900022-
dc.citation.woscount11-
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