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dc.contributor.authorIwakura, Izumien_US
dc.contributor.authorYabushita, Atsushien_US
dc.contributor.authorKobayashi, Takayoshien_US
dc.date.accessioned2014-12-08T15:12:09Z-
dc.date.available2014-12-08T15:12:09Z-
dc.date.issued2008-05-27en_US
dc.identifier.issn0009-2614en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.cplett.2008.03.003en_US
dc.identifier.urihttp://hdl.handle.net/11536/9320-
dc.description.abstractA transition state (TS) during Raman triggered oxidation of chloroform was directly observed by ultrafast spectroscopy using broadband visible sub-5 fs pulses. Changes in the molecular structures including the TSs along the reaction pathways were detected by the time-dependent instantaneous frequencies of vibrational modes. The Raman triggered oxidation of chloroform was found to be initiated by the excitation of vibrational levels through stimulated Raman processes involving the ground-state chloroform oxygen complex. (C) 2008 Published by Elsevier B.V.en_US
dc.language.isoen_USen_US
dc.titleObservation of transition state in Raman triggered oxidation of chloroform in the ground state by real-time vibrational spectroscopyen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.cplett.2008.03.003en_US
dc.identifier.journalCHEMICAL PHYSICS LETTERSen_US
dc.citation.volume457en_US
dc.citation.issue4-6en_US
dc.citation.spage421en_US
dc.citation.epage426en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000255953800029-
dc.citation.woscount9-
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