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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
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Nassar, Gamal M. | - |
| dc.contributor.author | Chung, Jeyon | - |
| dc.contributor.author | Cuc Kim Trinh | - |
| dc.contributor.author | El-Shehawy, Ashraf A. | - |
| dc.contributor.author | El-Barbary, Ahmed A. | - |
| dc.contributor.author | Kang, Youngjong | - |
| dc.contributor.author | Lee, Jae-Suk | - |
| dc.date.accessioned | 2023-05-03T11:19:36Z | - |
| dc.date.available | 2023-05-03T11:19:36Z | - |
| dc.date.issued | 2022-10 | - |
| dc.identifier.issn | 2046-2069 | - |
| dc.identifier.issn | 2046-2069 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/185214 | - |
| dc.description.abstract | Three 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.extent | 6 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | Royal Society of Chemistry | - |
| dc.title | 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 | - |
| dc.type | Article | - |
| dc.publisher.location | 영국 | - |
| dc.identifier.doi | 10.1039/d2ra04602d | - |
| dc.identifier.scopusid | 2-s2.0-85142933136 | - |
| dc.identifier.wosid | 000876953500001 | - |
| dc.identifier.bibliographicCitation | RSC Advances, v.12, no.48, pp 31180 - 31185 | - |
| dc.citation.title | RSC Advances | - |
| dc.citation.volume | 12 | - |
| dc.citation.number | 48 | - |
| dc.citation.startPage | 31180 | - |
| dc.citation.endPage | 31185 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
| dc.subject.keywordPlus | H ARYLATION | - |
| dc.subject.keywordPlus | POLYACRYLATE COPOLYMER | - |
| dc.subject.keywordPlus | POLYCONDENSATION | - |
| dc.subject.keywordPlus | DERIVATIVES | - |
| dc.subject.keywordPlus | CATALYST | - |
| dc.subject.keywordPlus | MOBILITY | - |
| dc.subject.keywordPlus | FUNCTIONALIZATION | - |
| dc.subject.keywordPlus | ACYLATION | - |
| dc.subject.keywordPlus | BROMIDES | - |
| dc.subject.keywordPlus | ALKYNES | - |
| dc.identifier.url | https://pubs.rsc.org/en/content/articlelanding/2022/RA/D2RA04602D | - |
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