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dc.contributor.authorIwakura, Izumien_US
dc.contributor.authorYabushita, Atsushien_US
dc.contributor.authorKobayashi, Takayoshien_US
dc.date.accessioned2014-12-08T15:07:35Z-
dc.date.available2014-12-08T15:07:35Z-
dc.date.issued2010-01-07en_US
dc.identifier.issn0009-2614en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.cplett.2009.11.029en_US
dc.identifier.urihttp://hdl.handle.net/11536/5980-
dc.description.abstractWe have found that photo-excited indigo carmine causes stepwise proton transfer to generate mono-alcohol intermediate, which immediately returns to the parent molecule [I. Iwakura, A. Yabushita, T. Kobayashi, Chem. Lett. 38 (2009) 1020]. The kinetic isotope effect in the proton transfer of this system has been studied by direct observation of the real-time molecular vibrational amplitude during the reaction including the transition state using a sub-5-fs laser pulse. The k(a)(H)/k(a)(D) ratio for the proton transfer after photo-excitation is observed to be 1.5 +/- 0.1. (C) 2009 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleKinetic isotope effect on the proton-transfer in indigo carmineen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.cplett.2009.11.029en_US
dc.identifier.journalCHEMICAL PHYSICS LETTERSen_US
dc.citation.volume484en_US
dc.citation.issue4-6en_US
dc.citation.spage354en_US
dc.citation.epage357en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000273051800053-
dc.citation.woscount10-
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