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A new class of organic semiconductors for solution processed OTFTs: Synthesis and characterization of pyrrolo-perylene derivatives with different end groups

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dc.contributor.authorPark, Kwang Hun-
dc.contributor.authorYun, Hui-Jun-
dc.contributor.authorLu, Wanxiang-
dc.contributor.authorChung, Dae Sung-
dc.contributor.authorKwon, Soon-Ki-
dc.contributor.authorKim, Yun-Hi-
dc.date.accessioned2022-12-26T23:16:46Z-
dc.date.available2022-12-26T23:16:46Z-
dc.date.issued2014-04-
dc.identifier.issn0143-7208-
dc.identifier.issn1873-3743-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/19079-
dc.description.abstractNew pyrrolo perylene derivatives, a new class of organic semiconductor, were designed for solution processed organic thin film transistors (OTFTs). Newly designed 2-(naphthalen-2-yl)thiophene end capped pyrrolo perylene, 3,10-bis(5-(naphthalen-2-yl)thiophen-2-yl)-1-(2-octyldodecyl)-1H-phenanthro[1,10,9,8-cdefg]carbazole (NTPP), and bithiophene end capped pyrrolo-perylene, 3,10-bis([2,2'-bithiophen]-5-yl)-1-(2-octyldodecyl)-1H-phenanthro[1,10,9,8-cdefg]carbazole (BTPP), were synthesized by Suzuki coupling and Stille coupling reaction, respectively. NTPP and BTPP showed good solubility in common organic solvents and were characterized by various spectroscopy. Solution processed OTFTs using BTPP exhibited high field-effect mobilities up to 0.11 cm(2) V-1 s(-1) an on/off ratio of 1 x 10(4) and a very small threshold voltage of 0 V. while OTFTs using NTPP exhibited far lower performances. The high mobility of BTPP is attributed to three dimensional multi-layered crystalline structure based on the results of the two dimensional grazing incidence X-ray diffraction pattern analysis and theoretical calculation using Gaussian, together with morphological study. (C) 2013 Elsevier Ltd. All rights reserved.-
dc.format.extent8-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titleA new class of organic semiconductors for solution processed OTFTs: Synthesis and characterization of pyrrolo-perylene derivatives with different end groups-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1016/j.dyepig.2013.12.001-
dc.identifier.scopusid2-s2.0-84892778526-
dc.identifier.wosid000331781600027-
dc.identifier.bibliographicCitationDyes and Pigments, v.103, pp 214 - 221-
dc.citation.titleDyes and Pigments-
dc.citation.volume103-
dc.citation.startPage214-
dc.citation.endPage221-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaEngineering-
dc.relation.journalResearchAreaMaterials Science-
dc.relation.journalWebOfScienceCategoryChemistry, Applied-
dc.relation.journalWebOfScienceCategoryEngineering, Chemical-
dc.relation.journalWebOfScienceCategoryMaterials Science, Textiles-
dc.subject.keywordPlusTHIN-FILM TRANSISTORS-
dc.subject.keywordPlusFIELD-EFFECT TRANSISTORS-
dc.subject.keywordPlusSMALL MOLECULES-
dc.subject.keywordPlusCOPOLYMER-
dc.subject.keywordPlusPOLYMERS-
dc.subject.keywordPlusMOBILITY-
dc.subject.keywordPlusEXCIMER-
dc.subject.keywordAuthorOTFT (organic thin film transistor)-
dc.subject.keywordAuthorSemiconductor-
dc.subject.keywordAuthorSolution process-
dc.subject.keywordAuthorPyrrolo-perylene-
dc.subject.keywordAuthorEnd-group effect-
dc.subject.keywordAuthorMobility-
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