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5 ',5 ''-(9,10-Bis((4-hexylphenyl)ethynyl) anthracene-2,6-diyl)bis(5-hexyl-2,2 '-bithiophene) as an Organic Semiconductor and its Application to Thin Film Transistors

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dc.contributor.authorBae, Suk Young-
dc.contributor.authorJo, So Young-
dc.contributor.authorKim, Kyung Hwan-
dc.contributor.authorLee, Tae Wan-
dc.contributor.authorChoi, Dong Hoon-
dc.date.accessioned2021-09-07T21:58:36Z-
dc.date.available2021-09-07T21:58:36Z-
dc.date.created2021-06-14-
dc.date.issued2011-
dc.identifier.issn1542-1406-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/115058-
dc.description.abstractNew anthracene-containing conjugated molecules have been synthesized through Stille coupling reaction. 2,6-Dibromo-9,10-bis(4-hexylphenyl) ethynyl) anthracene and 2,6-dibromo-9,10-bis(phenylethynyl) anthracene were reacted with tributyl (5'-hexyl-2,2'-bithiophen-5-yl) stannane to yield 5',5"-(9,10-bis(phenylethynyl) anthracene-2,6-diyl) bis(5-hexyl-2,2'-bithiophene), 1 and 5',5"-(9,10-bis((4-hexyl phenyl) ethynyl) anthracene-2,6-diyl) bis(5-hexyl-2,20-bithiophene), 2. The molecule, 2 only exhibit good solubility in common organic solvents and good self-film-forming properties. The semiconducting properties of the molecule, 2 were evaluated in organic thin film transistors (OTFTs). The molecule, 2 exhibits charge carrier mobilities-as high as 5.3 x 10(-3) cm(2) V-1 s(-1) (I-ON/I-OFF=2.43 x 10(5)) without thermal annealing process.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherTAYLOR & FRANCIS LTD-
dc.subjectHIGH-PERFORMANCE-
dc.subjectDERIVATIVES-
dc.subjectMOBILITY-
dc.title5 ',5 ''-(9,10-Bis((4-hexylphenyl)ethynyl) anthracene-2,6-diyl)bis(5-hexyl-2,2 '-bithiophene) as an Organic Semiconductor and its Application to Thin Film Transistors-
dc.typeArticle-
dc.contributor.affiliatedAuthorChoi, Dong Hoon-
dc.identifier.doi10.1080/15421406.2011.563718-
dc.identifier.wosid000290677300027-
dc.identifier.bibliographicCitationMOLECULAR CRYSTALS AND LIQUID CRYSTALS, v.538, pp.175 - 181-
dc.relation.isPartOfMOLECULAR CRYSTALS AND LIQUID CRYSTALS-
dc.citation.titleMOLECULAR CRYSTALS AND LIQUID CRYSTALS-
dc.citation.volume538-
dc.citation.startPage175-
dc.citation.endPage181-
dc.type.rimsART-
dc.type.docTypeArticle; Proceedings Paper-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaCrystallography-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryCrystallography-
dc.relation.journalWebOfScienceCategoryMaterials Science, Multidisciplinary-
dc.subject.keywordPlusHIGH-PERFORMANCE-
dc.subject.keywordPlusDERIVATIVES-
dc.subject.keywordPlusMOBILITY-
dc.subject.keywordAuthorAnthracene-
dc.subject.keywordAuthorbithiophene-
dc.subject.keywordAuthorconjugated molecules-
dc.subject.keywordAuthormobility-
dc.subject.keywordAuthororganic thin film transistor-
dc.subject.keywordAuthorsemiconductor-
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