Publication:
Fluorene-Dithienothiophene-S,S-dioxide Copolymers. Fine-Tuning for OLED Applications

dc.contributor.authorsOsken, Ipek; Gundogan, Ali Senol; Tekin, Emine; Eroglu, Mehmet S.; Ozturk, Turan
dc.date.accessioned2022-03-12T18:10:41Z
dc.date.accessioned2026-01-11T06:35:04Z
dc.date.available2022-03-12T18:10:41Z
dc.date.issued2013
dc.description.abstractThree groups of fluorene-dithieno[3,2-b;2',3'-d]-thiophene-S,S-dioxides (DTT-S,S-dioxide) copolymers, each having four different ratios of DTT-S,S-dioxide (5, 15, 25, and 50%) were successfully synthesized through Suzuki coupling method. While the first group copolymers PI had direct connection of fluorene to the peripheral thiophenes of DTT-S,S-dioxide, second group copolymers P2 had a thiophene extension between fluorene and DTT-S,S-dioxide, and in the third group, copolymers P3, fluorene had a connection with DTT-S,S-dioxide through the phenyl moiety of DTT. Absorbance and emission measurements of first two groups P1 and P2 displayed a regular bathochromic shift with increasing content of DTT-S,S-dioxide, which was more clearly observed in their solid state fluorescence measurements. Introduction of thiophene to the peripherals of the DTT-S,S-dioxide in copolymers P2 caused even further bathochromic shift in absorbances and emissions. As the absorbance and emission of PI went up to 447 and 558 nm in solution, respectively, P2 had them at 472 and 592 nm, respectively. In solid state, emissions of 131 and P2 even went further up to 585 and 646 nm, respectively. The bathochromic trend of 131 and P2 became opposite with absorbance and solid state emission of P3, which had a hypsochromic shift with increasing content of DTT-S,S-dioxide. Solid state emission of P3, particularly the copolymers having 5, 15 and 50% DTT-S,S-dioxide, covered a wide region between 400 and 675 nm. A spread of colors from light blue (border of white) to red through green and yellow was obtained with the OLED applications of the copolymers. Their optical and electronic band gaps varied between 2.17 and 2.99 eV and between 2.68 and 3.57 eV, respectively. While the highest quantum yield was obtained with P2 (5%) as 0.66, the lowest was observed with P2 (50%) as 0.03. Almost all of the polymers displayed good thermal stabilities. No weight loss was observed with the copolymers P2 (5-15%) and P3 up to 400 degrees C.
dc.identifier.doi10.1021/ma4016592
dc.identifier.eissn1520-5835
dc.identifier.issn0024-9297
dc.identifier.urihttps://hdl.handle.net/11424/231398
dc.identifier.wosWOS:000328436800005
dc.language.isoeng
dc.publisherAMER CHEMICAL SOC
dc.relation.ispartofMACROMOLECULES
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectLIGHT-EMITTING-DIODES
dc.subjectCONJUGATED POLYMERS
dc.subjectELECTROLUMINESCENCE
dc.subjectPHOTOLUMINESCENCE
dc.titleFluorene-Dithienothiophene-S,S-dioxide Copolymers. Fine-Tuning for OLED Applications
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage9210
oaire.citation.issue23
oaire.citation.startPage9202
oaire.citation.titleMACROMOLECULES
oaire.citation.volume46

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