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dc.contributor.authorYuzawa, Tetsuroen_US
dc.contributor.authorHamaguchi, Hiro-oen_US
dc.date.accessioned2014-12-08T15:06:34Z-
dc.date.available2014-12-08T15:06:34Z-
dc.date.issued2010-07-15en_US
dc.identifier.issn0022-2860en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.molstruc.2010.04.031en_US
dc.identifier.urihttp://hdl.handle.net/11536/5137-
dc.description.abstractThe mechanism of the photoisomerization of 9-cis retinal has been studied by nanosecond time-resolved infrared spectroscopy. A cyclohexane solution of 9-cis retinal was photoexcited at 349 nm and the subsequent photodynamics were traced. A singular value decomposition (SVD) analysis of the time-resolved infrared data shows that there are two distinct isomerization pathways. One is the triplet pathway that takes place in the picosecond time regime from 9-cis to all-trans. The other involves the energy transfer between the all-trans triplet state and the 9-cis ground state with the resultant 9-cis triplet state subsequently reproducing the all-trans by fast isomerization on the triplet potential surface. This quantum chain process occurs in the microsecond time regime. (C) 2010 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectTriplet quantum chainen_US
dc.subjectPhotoisomerizationen_US
dc.subject9-Cis retinalen_US
dc.subjectNanosecond time-resolved infrared spectroscopyen_US
dc.subjectPhotodynamicsen_US
dc.titleTriplet quantum chain process in the photoisomerization of 9-cis retinal as revealed by nanosecond time-resolved infrared spectroscopyen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.molstruc.2010.04.031en_US
dc.identifier.journalJOURNAL OF MOLECULAR STRUCTUREen_US
dc.citation.volume976en_US
dc.citation.issue1-3en_US
dc.citation.spage414en_US
dc.citation.epage418en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000280244400057-
dc.citation.woscount2-
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