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dc.contributor.authorWu, Chung-Wenen_US
dc.contributor.authorLin, Hong-Cheuen_US
dc.date.accessioned2014-12-08T15:15:37Z-
dc.date.available2014-12-08T15:15:37Z-
dc.date.issued2006-10-17en_US
dc.identifier.issn0024-9297en_US
dc.identifier.urihttp://dx.doi.org/10.1021/ma061770jen_US
dc.identifier.urihttp://hdl.handle.net/11536/11665-
dc.description.abstractTo decrease the aggregation phenomena and improve the luminescent properties of polyfluorenes (PFs), a series of novel kinked and hyperbranched carbazole units were copolymerized by the Suzuki coupling polycondensation reaction to introduce disorder packing into the copolymer backbones. The thermal, photophysical, electrochemical, and electroluminescent properties of the copolymers were investigated. All of these polymers possess excellent thermal stability with onset decomposition temperatures at 407-466 degrees C and glass transition temperatures at 109-140 degrees C. Photoluminescent (PL) studies showed that these polymers were promising blue light-emitting materials, which exhibited high quantum efficiencies in solution and solid states. Long wavelength emissions at 500-600 nm, which were typical for PFs due to their self-aggregation in the solid state, were suppressed in these polymers. Annealing studies under air showed both improved thermal and photoluminescence stability of the polymers. It was proven that HOMO energy levels of the copolymers can be enlarged by increasing the carbazole content in the electrochemical measurements; hence, the hole injection was greatly enhanced. Pure-blue electroluminescence (EL) spectra with narrow fwhm (full width at the half-maximum) values (39-42 nm) and negligible low-energy excimer emission bands were successfully achieved, indicating that these copolymers could be good candidates for blue light-emitting materials.en_US
dc.language.isoen_USen_US
dc.titleSynthesis and characterization of kinked and hyperbranched carbazole/fluorene-based copolymersen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/ma061770jen_US
dc.identifier.journalMACROMOLECULESen_US
dc.citation.volume39en_US
dc.citation.issue21en_US
dc.citation.spage7232en_US
dc.citation.epage7240en_US
dc.contributor.department材料科學與工程學系zh_TW
dc.contributor.departmentDepartment of Materials Science and Engineeringen_US
dc.identifier.wosnumberWOS:000241106900012-
dc.citation.woscount51-
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