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dc.contributor.authorChang, CWen_US
dc.contributor.authorKao, YTen_US
dc.contributor.authorDiau, EWGen_US
dc.date.accessioned2014-12-08T15:40:46Z-
dc.date.available2014-12-08T15:40:46Z-
dc.date.issued2003-06-04en_US
dc.identifier.issn0009-2614en_US
dc.identifier.urihttp://dx.doi.org/10.1016/S0009-2614(03)00645-6en_US
dc.identifier.urihttp://hdl.handle.net/11536/27795-
dc.description.abstractThe nonradiative dynamics of DCM in hexane have been investigated using femtosecond fluorescence up conversion technique at three excitation wavelengths (400, 445 and 480 nm). The S, lifetime was observed to be 9.8 +/- 0.5 ps, which is independent of the excitation and the fluorescence wavelengths. The observed S, lifetimes of DCJT and DCJTB are slower than those of DCM and DCMB by one order of magnitude, indicating the significance of the twisting motion of the amino group affecting the S, nonradiative dynamics. TDDFT calculations suggest that an intersystem crossing is responsible for the observed S, dynamics of DCM in nonpolar solvent. (C) 2003 Elsevier Science B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleFluorescence lifetime and nonradiative relaxation dynamics of DCM in nonpolar solventen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/S0009-2614(03)00645-6en_US
dc.identifier.journalCHEMICAL PHYSICS LETTERSen_US
dc.citation.volume374en_US
dc.citation.issue1-2en_US
dc.citation.spage110en_US
dc.citation.epage118en_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:000183595600019-
dc.citation.woscount12-
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