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Polymers based on thieno[3,4-c]pyrrole-4,6-dione and pyromellitic diimide by CH-CH arylation reaction for high-performance thin-film transistors

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dc.contributor.authorNassar, Gamal M.-
dc.contributor.authorChung, Jeyon-
dc.contributor.authorCuc Kim Trinh-
dc.contributor.authorEl-Shehawy, Ashraf A.-
dc.contributor.authorEl-Barbary, Ahmed A.-
dc.contributor.authorKang, Youngjong-
dc.contributor.authorLee, Jae-Suk-
dc.date.accessioned2023-05-03T11:19:36Z-
dc.date.available2023-05-03T11:19:36Z-
dc.date.issued2022-10-
dc.identifier.issn2046-2069-
dc.identifier.issn2046-2069-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/185214-
dc.description.abstractThree homopolymers were successfully synthesized by direct CH-CH arylation polymerization of thieno[3,4-c]pyrrole-4,6-dione or pyromellitic diimide derivatives affording highly purified polymers with high molecular weights (43.0-174.7 K). Thieno[3,4-c]pyrrole-4,6-dione and pyromellitic diimide derivatives are considered as electron-withdrawing units. The synthesized homopolymers P1, P2, and P3 showed band gaps in the range of 2.13-2.08 eV, respectively. The electron mobilities of the three homopolymers have been investigated. The thin film transistor for P1 prepared by the eutectic-melt-assisted nanoimprinting method achieved an electron mobility of 2.11 x 10(-3) cm(2) s(-1) V-1. Based on the obtained results, the synthesized polymers can be used as potential electron acceptors in solar cell applications.-
dc.format.extent6-
dc.language영어-
dc.language.isoENG-
dc.publisherRoyal Society of Chemistry-
dc.titlePolymers based on thieno[3,4-c]pyrrole-4,6-dione and pyromellitic diimide by CH-CH arylation reaction for high-performance thin-film transistors-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1039/d2ra04602d-
dc.identifier.scopusid2-s2.0-85142933136-
dc.identifier.wosid000876953500001-
dc.identifier.bibliographicCitationRSC Advances, v.12, no.48, pp 31180 - 31185-
dc.citation.titleRSC Advances-
dc.citation.volume12-
dc.citation.number48-
dc.citation.startPage31180-
dc.citation.endPage31185-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusH ARYLATION-
dc.subject.keywordPlusPOLYACRYLATE COPOLYMER-
dc.subject.keywordPlusPOLYCONDENSATION-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusCATALYST-
dc.subject.keywordPlusMOBILITY-
dc.subject.keywordPlusFUNCTIONALIZATION-
dc.subject.keywordPlusACYLATION-
dc.subject.keywordPlusBROMIDES-
dc.subject.keywordPlusALKYNES-
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2022/RA/D2RA04602D-
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