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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.authorKobayashi, Takayoshien_US
dc.date.accessioned2014-12-08T15:23:45Z-
dc.date.available2014-12-08T15:23:45Z-
dc.date.issued2012en_US
dc.identifier.issn1463-9076en_US
dc.identifier.urihttp://hdl.handle.net/11536/16570-
dc.description.abstractAllyl phenyl ether has an absorption band in the ultraviolet region (lambda < 400 nm); therefore, irradiation with few-optical-cycle ultraviolet pulses (lambda = 360-440 nm) causes a transition to the ultraviolet band, which leads to an electronic state and a photo-Claisen rearrangement (radical reaction) in the electronic excited state. However, the reaction scheme of allyl phenyl ether under irradiation with few-optical-cycle visible pulses (lambda = 525-725 nm) was determined to be same as that of the thermal Claisen rearrangement ([3,3]-sigmatropic rearrangement), which is symmetry-allowed in the electronic ground state. Photo-excitation with few-optical cycle visible pulses below the absorption band induces a photo-impulsive reaction in the electronic ground state without electronic excitation, of which the trigger scheme is different from that of photoreaction or thermal-reaction. The photo-impulsive reaction in the electronic ground state is highly possible as a novel reaction scheme.en_US
dc.language.isoen_USen_US
dc.titlePhoto-impulsive reactions in the electronic ground state without electronic excitation: non-photo, non-thermal chemical reactionsen_US
dc.typeArticleen_US
dc.identifier.journalPHYSICAL CHEMISTRY CHEMICAL PHYSICSen_US
dc.citation.volume14en_US
dc.citation.issue27en_US
dc.citation.epage9696en_US
dc.contributor.department電子物理學系zh_TW
dc.contributor.departmentDepartment of Electrophysicsen_US
dc.identifier.wosnumberWOS:000305581500020-
dc.citation.woscount6-
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