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dc.contributor.authorBhongale, CJen_US
dc.contributor.authorChang, CWen_US
dc.contributor.authorDiau, EWGen_US
dc.contributor.authorHsu, CSen_US
dc.contributor.authorDong, YQen_US
dc.contributor.authorTang, BZen_US
dc.date.accessioned2014-12-08T15:17:20Z-
dc.date.available2014-12-08T15:17:20Z-
dc.date.issued2006-02-26en_US
dc.identifier.issn0009-2614en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.cplett.2005.12.017en_US
dc.identifier.urihttp://hdl.handle.net/11536/12604-
dc.description.abstractNanostructures of 1,1,2,3,4,5-hexaphenylsilole (HPS) of various types were obtained on simple reprecipitation with THF as solvent and water as non-solvent. The formation and evolution of these nanostructures were monitored with scanning electron microscopy. Using picosecond time-correlated single-photon counting, we observed enhanced emission and fluorescence lifetimes at volume fractions 70-90% of added water. We report the first enhanced color-tunable emissions of a conjugated organic compound (HPS) due to the formation of nanoflowers, nanoglobules and microglobules, and provide time scales for those nanostructures and the corresponding intermolecular interactions in the aggregates. (c) 2005 Elsevier B.V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleFormation of nanostructures of hexaphenylsilole with enhanced color-tunable emissionsen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.cplett.2005.12.017en_US
dc.identifier.journalCHEMICAL PHYSICS LETTERSen_US
dc.citation.volume419en_US
dc.citation.issue4-6en_US
dc.citation.spage444en_US
dc.citation.epage449en_US
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000235675000027-
dc.citation.woscount33-
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