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Synthesis of novel asymmetric oligomers based on oligothiophene-naphthalene molecules and solution-processable p-channel organic thin film transistors

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dc.contributor.authorJang, S.H.-
dc.contributor.authorShin, M.-G.-
dc.contributor.authorPark, J.H.-
dc.contributor.authorChung, D.S.-
dc.contributor.authorPark, C.E.-
dc.contributor.authorKim, Y.-H.-
dc.contributor.authorLee, S.-G.-
dc.contributor.authorKwon, S.-K.-
dc.date.accessioned2024-12-03T03:30:58Z-
dc.date.available2024-12-03T03:30:58Z-
dc.date.issued2010-00-
dc.identifier.issn1738-7558-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/73827-
dc.description.abstractA series of novel thiophene-naphthalene based asymmetric oligomers for organic thin film transistors (OTFTs) were synthesized by Suzuki cross-coupling reaction between 2-bromo-6-decylnaphthalene and 2-decylthiophene, 2-decyl bithiophene, or 1-decylbenzene, respectively. Remarkably, AON-1 and AON-3 showed good solubility in common solvents. The fabricated devices showed the hole field-effect mobility of 1.4 × 10-2 cm2/Vs for AO, 1.5 × 10-2 cm2/Vs for AON-1, and 3.7 ×10 2 cm-2/Vs for AON-3.-
dc.format.extent2-
dc.language영어-
dc.language.isoENG-
dc.titleSynthesis of novel asymmetric oligomers based on oligothiophene-naphthalene molecules and solution-processable p-channel organic thin film transistors-
dc.typeArticle-
dc.identifier.scopusid2-s2.0-79960021445-
dc.identifier.bibliographicCitationProceedings of International Meeting on Information Display, pp 699 - 700-
dc.citation.titleProceedings of International Meeting on Information Display-
dc.citation.startPage699-
dc.citation.endPage700-
dc.type.docTypeConference Paper-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscopus-
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