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Energy transfer and phosphorescence-quenching dynamics in a phosphorescent host-guest system

dc.citation.epage56en_US
dc.citation.issueen_US
dc.citation.spage52en_US
dc.citation.volume561en_US
dc.citation.woscount0
dc.contributor.authorChang, Chih-Weien_US
dc.contributor.authorLee, Rei-Yunen_US
dc.contributor.authorDiau, Eric Wei-Guangen_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.date.accessioned2014-12-08T15:29:23Z
dc.date.available2014-12-08T15:29:23Z
dc.date.issued2013-03-13en_US
dc.description.abstractWe investigated the energy transfer dynamics in a phosphorescent host-guest system. Two spirobifluorene derivatives, [2,7-bis(2,2-diphenylvinyl)-9,9'-spirobifluorene] (DPVSBF) and [2,7-bis(1,2,2-triphenylvinyl)-9,9'-spirobifluorene] (TPVSBF), were doped with the red phosphor complex [Os(bpftz)(2)(PPh2Me)(2)] (Os-R). The two hosts exhibit similar host-to-guest energy transfer efficiencies; however, the backward energy transfer from the Os-R complex to TPVSBF is slower than that from Os-R to DPVSBF. Quantum chemical calculations suggest that the backward energy transfer dynamics are related to the host's triplet-state energy level. The greater energy of the TPVSBF triplet state compared to that of DPVSBF plays a crucial role in its ability to confine triplet excitons in Os-R. (C) 2013 Elsevier B. V. All rights reserved.en_US
dc.identifier.doi10.1016/j.cplett.2013.01.038en_US
dc.identifier.issn0009-2614en_US
dc.identifier.journalCHEMICAL PHYSICS LETTERSen_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.cplett.2013.01.038en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/21174
dc.identifier.wosnumberWOS:000315279600009
dc.language.isoen_USen_US
dc.titleEnergy transfer and phosphorescence-quenching dynamics in a phosphorescent host-guest systemen_US
dc.typeArticleen_US

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