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dc.contributor.authorIwakural, Izumien_US
dc.contributor.authorYabushita, Atsushien_US
dc.date.accessioned2017-04-21T06:56:50Z-
dc.date.available2017-04-21T06:56:50Z-
dc.date.issued2016-03-15en_US
dc.identifier.issn0009-2673en_US
dc.identifier.urihttp://dx.doi.org/10.1246/bcsj.20150242en_US
dc.identifier.urihttp://hdl.handle.net/11536/133474-
dc.description.abstractFemtochemistry began from the observation of transition states (TSs) in gas-phase photoreactions. Later developments in visible ultrashort laser pulses enabled visualization of real-time changes in the molecular vibrational modes during photo reactions, including those in the liquid phase. However, TSs in thermal reactions could still not be studied, because the conventional femtosecond laser pulse cannot trigger chemical reactions in the electronic ground state. In the present work, a visible ultrashort laser pulse was used to cause an induced Raman process, whereby Raman active molecular vibrational modes were excited in the electronic ground states, which triggers the reaction induced by coherent molecular vibrational excitation in the electronic ground state just after photo excitation. Using the "reaction by coherent molecular vibration", we have successfully observed the TSs in a "thermal" reaction, thermal Claisen rearrangement.en_US
dc.language.isoen_USen_US
dc.titleDevelopment of Novel Reactions Induced by Coherent Molecular Vibrational Excitation and Direct Observation of Molecular Structural Change during "Thermal" Reactionsen_US
dc.identifier.doi10.1246/bcsj.20150242en_US
dc.identifier.journalBULLETIN OF THE CHEMICAL SOCIETY OF JAPANen_US
dc.citation.volume89en_US
dc.citation.issue3en_US
dc.citation.spage296en_US
dc.citation.epage307en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000372775100003en_US
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