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dc.contributor.authorIwakura, Izumien_US
dc.contributor.authorYabushita, Atsushien_US
dc.contributor.authorLiu, Junen_US
dc.contributor.authorOkamura, Kotaroen_US
dc.contributor.authorKezuka, Satokoen_US
dc.contributor.authorKobayashi, Takayoshien_US
dc.date.accessioned2014-12-08T15:32:36Z-
dc.date.available2014-12-08T15:32:36Z-
dc.date.issued2013en_US
dc.identifier.issn0033-4545en_US
dc.identifier.urihttp://hdl.handle.net/11536/22811-
dc.identifier.urihttp://dx.doi.org/10.1351/PAC-CON-12-12-01en_US
dc.description.abstractTime-resolved vibration spectroscopy is the only known way to directly observe reaction processes. In this work, we measure time-resolved vibration spectra of the Claisen rearrangement triggered and observed by few-optical-cycle pulses. Changes in molecular structure during the reaction, including its transition states (TSs), are elucidated by observing the transient changes of molecular vibration wavenumbers. We pump samples with visible ultrashort pulses of shorter duration than the molecular vibration period, and with photon energies much lower than the minimum excitation energy of the sample. The results indicate that the "nonthermal Claisen rearrangement" can be triggered by visible few-optical-cycle pulses exciting molecular vibrations in the electronic ground state of the sample, which replaces the typical thermal Claisen rearrangement.en_US
dc.language.isoen_USen_US
dc.subjectlaser spectroscopyen_US
dc.subjectreaction mechanismsen_US
dc.subjectrearrangementsen_US
dc.titleA new reaction mechanism of Claisen rearrangement induced by few-optical-cycle pulses: Demonstration of nonthermal chemistry by femtosecond vibrational spectroscopyen_US
dc.typeArticleen_US
dc.identifier.doi10.1351/PAC-CON-12-12-01en_US
dc.identifier.journalPURE AND APPLIED CHEMISTRYen_US
dc.citation.volume85en_US
dc.citation.issue10en_US
dc.citation.spage1991en_US
dc.citation.epage2004en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000325083900008-
dc.citation.woscount0-
Appears in Collections:Articles