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Relaxation Dynamics and Structural Characterization of Organic Nanobelts with Aggregation-Induced Emission

dc.citation.epage15146en_US
dc.citation.issue28en_US
dc.citation.volume116en_US
dc.citation.woscount9
dc.contributor.authorChang, Chih-Weien_US
dc.contributor.authorBhongale, Chetan Jagdishen_US
dc.contributor.authorLee, Chi-Shenen_US
dc.contributor.authorHuang, Wei-Kaien_US
dc.contributor.authorHsu, Chain-Shuen_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.accessioned2014-12-08T15:23:53Z
dc.date.available2014-12-08T15:23:53Z
dc.date.issued1970-01-01en_US
dc.description.abstract"We prepared the fluorescent nanobelts of cyano-substituted 1,4-distyrylbenzene derivative (CNDSB) with the reprecipitation method. CNDSB is nonemissive in solution but with strong aggregation-induced emission (AIE) in belt-like structure. The molecular structure predicted by quantum chemical calculations indicates a twisted conformation of CNDSB monomer, while the solid-state X-ray structure of the CNDSB crystal features herringbone-type arrangement and three benzene rings arrange in nearly planar conformation. Femto- and picosecond time-resolved fluorescence spectroscopy are implemented to study the photophysics and the origin of the ME effect in CNDSB nanobelts. The fluorescence quenching of CNDSB in THF solution arises from the efficient nonradiative isomerization channel. In this study, the fluorescence decay of CNDSB embedded in poly(methyl methacrylate) matrix is slowed down due to the restriction of intra:molecular motions in the solid matrix. In nanobelt structure, the fluorescence lifetime further increases due to the intermolecular interaction between H-type aggregates. Both the steady-state and time-resolved studies suggests that there are at least two different packing structures might exist in nanobelts, and the relative composition of these two different structures gradually changes in different sizes of nanobelts."en_US
dc.identifier.issn1932-7447en_US
dc.identifier.journalJOURNAL OF PHYSICAL CHEMISTRY Cen_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/16622
dc.identifier.wosnumberWOS:000306503200050
dc.language.isoen_USen_US
dc.titleRelaxation Dynamics and Structural Characterization of Organic Nanobelts with Aggregation-Induced Emissionen_US
dc.typeArticleen_US

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