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dc.contributor.authorIwakura, Izumien_US
dc.contributor.authorYabushita, Atsushien_US
dc.contributor.authorKobayashi, Takayoshien_US
dc.date.accessioned2014-12-08T15:12:08Z-
dc.date.available2014-12-08T15:12:08Z-
dc.date.issued2011-02-15en_US
dc.identifier.issn0009-2673en_US
dc.identifier.urihttp://dx.doi.org/10.1246/bcsj.20100269en_US
dc.identifier.urihttp://hdl.handle.net/11536/9297-
dc.description.abstractDirect observation of the molecular structural change during chemical reactions including transition states is desirable to fully clarify the mechanism of chemical reactions. Time-dependent frequency variations in molecular vibration modes reflect structural change in transition states. Ultrafast changes in molecular structure during bond breaking and bond reformation can be clearly visualized using ultrafast spectroscopy. This study elucidated molecular structural information in states along the chemical reaction including transition state in the proton transfer of indigodisulfonate salt. The photoexcited proton transfer was found to follow a stepwise pathway. The monoalcohol intermediate generated by the proton transfer was found to return immediately to the original indigo without proton-transfer configuration. This back reaction of this is the reason for the ultra-photostability of indigo over extremely long exposure to light. This shows that real-time vibrational spectroscopy by a few femtosecond pulse laser enables the observation of dynamic behavior of molecular vibrations during chemical reactions, leading to the clarification of reaction mechanisms or the development of new chemical reactions.en_US
dc.language.isoen_USen_US
dc.titleTransition State in a Prevented Proton Transfer Observed in Real Timeen_US
dc.typeArticleen_US
dc.identifier.doi10.1246/bcsj.20100269en_US
dc.identifier.journalBULLETIN OF THE CHEMICAL SOCIETY OF JAPANen_US
dc.citation.volume84en_US
dc.citation.issue2en_US
dc.citation.spage164en_US
dc.citation.epage171en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000288287500005-
dc.citation.woscount6-
Appears in Collections:Articles