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dc.contributor.authorChang, Chih-Weien_US
dc.contributor.authorSolling, Theis I.en_US
dc.contributor.authorDiau, Eric Wei-Guangen_US
dc.date.accessioned2018-08-21T05:54:32Z-
dc.date.available2018-08-21T05:54:32Z-
dc.date.issued2017-10-16en_US
dc.identifier.issn0009-2614en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.cplett.2017.07.039en_US
dc.identifier.urihttp://hdl.handle.net/11536/146077-
dc.description.abstractUltrafast intersystem crossing dynamics of fluorenone in gas and condensed phases were investigated by time-resolved mass spectrometry and fluorescence up-conversion spectroscopy. The former shows the ultrafast Franck-Condon relaxation and the internal conversion dynamics of isolated fluorenone in the gas phase. The latter reveals that the vibrational relaxation time is 2.2 ps and a 110 ps fluorescence lifetime of fluorenone in hexane. The fluorescence lifetime in acetonitrile and dimethylsulfoxide is 16 ns and 15.1 ns, respectively. The potential energy surface along the C=O out of plane bending motion shows that this coordinate is important for ISC in both polar and non-polar solvents. (C) 2017 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.subjectFluorenoneen_US
dc.subjectTime-resolved mass spectroscopyen_US
dc.subjectTime-resolved fluorescence spectroscopyen_US
dc.subjectIntersystem crossingen_US
dc.titleRevisiting the photophysics of 9-fluorenone: Ultrafast time-resolved fluorescence and theoretical studiesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.cplett.2017.07.039en_US
dc.identifier.journalCHEMICAL PHYSICS LETTERSen_US
dc.citation.volume686en_US
dc.citation.spage218en_US
dc.citation.epage222en_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:000410844000035en_US
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