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Cited 39 time in webofscience Cited 43 time in scopus
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dc.contributor.authorDang, TTM-
dc.contributor.authorPark, SJ-
dc.contributor.authorPark, JW-
dc.contributor.authorChung, DS-
dc.contributor.authorPark, CE-
dc.contributor.authorKim, YH-
dc.contributor.authorKwon, SK-
dc.date.accessioned2016-04-01T01:30:22Z-
dc.date.available2016-04-01T01:30:22Z-
dc.date.created2009-02-28-
dc.date.issued2007-11-15-
dc.identifier.issn0887-624X-
dc.identifier.other2007-OAK-0000007291-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/23081-
dc.description.abstractPoly{2,6-bis(3-dodecylthiophen-2-yl)benzo[1,2-b;4,5-b']dithiophene] (PTBT) was synthesized, via oxidative polymerization by oxidative agent (FeCl3). The mole ratio of FeCl3 and monomer (3.5: 1), and keeping low temperature during the dropping of diluted catalyst were very important for the polymerization without crosslinking. The PTBT was confirmed by H-1 NMR, FTIR spectra, and elemental analysis. The PTBT has very good solubility in organic solvents such as chloroform, tetrahydrofuran, etc, and good thermal stability with T-g of 164 degrees C. The PTBT shows UV-optical absorption at 406 nm and photoluminescence (PL) spectroscopy at 504 mn in a film. The highest occupied molecular orbital (HOMO) energy of the polymer is -5.71 eV by measuring cyclic voltammetry (CV). A solution-processed polymer thin film transistor device shows a mobility of 3 X 10(-5) - 8 X 10(-5) cm(2) V-1 s(-1), and an on/off current ratio of 10(4). (c) 2007 Wiley Periodicals, Inc.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherJOHN WILEY & SONS INC-
dc.relation.isPartOfJOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY-
dc.subjectbenzodithiophene-
dc.subjectconducting polymers-
dc.subjectOTFT-
dc.subjectoxidative polymerization-
dc.subjectsolution properties-
dc.subjectspin coating-
dc.subjectthiophene-
dc.subjectBLUE-
dc.subjectPOLYMERS-
dc.subjectSEMICONDUCTORS-
dc.subjectMOBILITY-
dc.subjectDEVICES-
dc.subjectPURITY-
dc.titleSynthesis and characterization of poly(benzodithiophene) derivative for organic thin film transistors-
dc.typeArticle-
dc.contributor.college화학공학과-
dc.identifier.doi10.1002/POLA.22272-
dc.author.googleDang, TTM-
dc.author.googlePark, SJ-
dc.author.googlePark, JW-
dc.author.googleChung, DS-
dc.author.googlePark, CE-
dc.author.googleKim, YH-
dc.author.googleKwon, SK-
dc.relation.volume45-
dc.relation.issue22-
dc.relation.startpage5277-
dc.relation.lastpage5284-
dc.contributor.id10104044-
dc.relation.journalJOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationJOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, v.45, no.22, pp.5277 - 5284-
dc.identifier.wosid000250788600024-
dc.date.tcdate2019-01-01-
dc.citation.endPage5284-
dc.citation.number22-
dc.citation.startPage5277-
dc.citation.titleJOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY-
dc.citation.volume45-
dc.contributor.affiliatedAuthorPark, CE-
dc.identifier.scopusid2-s2.0-35748965603-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc36-
dc.description.scptc40*
dc.date.scptcdate2018-05-121*
dc.type.docTypeArticle-
dc.subject.keywordAuthorbenzodithiophene-
dc.subject.keywordAuthorconducting polymers-
dc.subject.keywordAuthorOTFT-
dc.subject.keywordAuthoroxidative polymerization-
dc.subject.keywordAuthorsolution properties-
dc.subject.keywordAuthorspin coating-
dc.subject.keywordAuthorthiophene-
dc.relation.journalWebOfScienceCategoryPolymer Science-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaPolymer Science-

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박찬언PARK, CHAN EON
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