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dc.contributor.authorHuang, Chiung-Weien_US
dc.contributor.authorLee, Yaw-Changen_US
dc.contributor.authorLee, Yuan-Pernen_US
dc.date.accessioned2014-12-08T15:07:02Z-
dc.date.available2014-12-08T15:07:02Z-
dc.date.issued2010-04-28en_US
dc.identifier.issn0021-9606en_US
dc.identifier.urihttp://dx.doi.org/10.1063/1.3386578en_US
dc.identifier.urihttp://hdl.handle.net/11536/5503-
dc.description.abstractIrradiation of a p-H(2) matrix containing Cl(2) and CS(2) at 3.3 K with laser emission at 340 nm followed by annealing of the matrix produced main features at 1479.5 and 1480.8 cm(-1). These lines are attributed to v(1) (SCS antisymmetric stretching) mode of ClSCS. Irradiation of the matrix at 355 nm decomposes ClSCS. Products CS (1272.2 and 1271.1 cm(-1)), ClCS (1193.9/1191.9 and 637.5 cm(-1)), and ClSC (1137.0 cm(-1)) were observed upon annealing. The assignments were based on comparison of observed vibrational wavenumbers and (13)C- and (34)S-isotopic ratios with those predicted with density-functional theories (B3LYP and BPW91/aug-cc-pVTZ). These results demonstrate that the cage effect of solid p-H(2) is diminished so that isolated Cl was produced via photodissociation of Cl(2) in situ and subsequently reacted with CS(2) to form ClSCS, but not ClC(=vS)SCl, upon annealing; typically ClC(vS)SCl was produced as the major product on irradiation of noble-gas matrices containing Cl(2) and CS(2). Observation of ClSCS but not ClCS(2) is consistent with the theoretical prediction that only formation of the former proceeds via a barrierless path. Similarly, upon irradiation of ClSCS at 355 nm, Cl, CS, and CS(2) were produced; subsequent annealing of the irradiated matrix produced ClSC and ClCS via barrierless paths. c 2010 American Institute of Physics. [doi: 10.1063/1.3386578]en_US
dc.language.isoen_USen_US
dc.titleDiminished cage effect in solid p-H(2): Infrared spectra of CISCS, CICS, and CISC in an irradiated p-H(2) matrix containing Cl(2) and CS(2)en_US
dc.typeArticleen_US
dc.identifier.doi10.1063/1.3386578en_US
dc.identifier.journalJOURNAL OF CHEMICAL PHYSICSen_US
dc.citation.volume132en_US
dc.citation.issue16en_US
dc.citation.spageen_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
Appears in Collections:Articles