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dc.contributor.author Palai, Akshaya Kumar -
dc.contributor.author Kumar, Amit -
dc.contributor.author Sim, Kyoseung -
dc.contributor.author Kwon, Jaehyuk -
dc.contributor.author Shin, Tae Joo -
dc.contributor.author Jang, Soonmin -
dc.contributor.author Cho, Sungwoo -
dc.contributor.author Park, Seung-Un -
dc.contributor.author Pyo, Seungmoon -
dc.date.available 2017-07-11T05:42:12Z -
dc.date.created 2017-04-10 -
dc.date.issued 2016 -
dc.identifier.issn 1144-0546 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/2794 -
dc.description.abstract A series of symmetrically arylthiophenyl-functionalized diketopyrrolopyrrole (DPP) derivatives were synthesized via palladium-catalyzed direct C-H arylation to develop an active material for organic electronic devices. The properties of DPPs could be tuned by simple variation of the end groups such as t-butylphenyl, cyanophenyl and methoxynaphthyl. The effect of the substituent on the optical, electrochemical, and thermal properties of DPPs was evaluated using UV-visible spectroscopy, cyclic voltammetry, and thermogravimetric analysis. The morphology and molecular packing of thin-films of DPPs were analyzed by atomic force microscopy (AFM), density functional theory (DFT) calculations, and two-dimensional grazing incidence X-ray diffraction (2D-GIXD) experiments. Utilization of the synthesized DPPs as channel materials in organic field-effect transistors was demonstrated. © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2016. -
dc.publisher Royal Society of Chemistry -
dc.title Facile synthesis of arylthiophenyl-functionalized diketopyrrolopyrrole derivatives via direct C-H arylation: characterization and utilization in organic electronic devices -
dc.type Article -
dc.identifier.doi 10.1039/c5nj02631h -
dc.identifier.scopusid 2-s2.0-84953299104 -
dc.identifier.bibliographicCitation New Journal of Chemistry, v.40, no.1, pp.385 - 392 -
dc.subject.keywordPlus Absorption Spectroscopy -
dc.subject.keywordPlus Aromatic Compound -
dc.subject.keywordPlus Article -
dc.subject.keywordPlus Arylation -
dc.subject.keywordPlus Arylthiophenyl -
dc.subject.keywordPlus Atomic Force Microscopy -
dc.subject.keywordPlus Catalyst -
dc.subject.keywordPlus CHARGE-TRANSPORT -
dc.subject.keywordPlus Chemical Bond -
dc.subject.keywordPlus Chemical Structure -
dc.subject.keywordPlus Crystallinity -
dc.subject.keywordPlus Cyclic Potentiometry -
dc.subject.keywordPlus Density Functional Theory -
dc.subject.keywordPlus Electron -
dc.subject.keywordPlus FIELD-EFFECT TRANSISTORS -
dc.subject.keywordPlus Field Effect Transistor -
dc.subject.keywordPlus Film -
dc.subject.keywordPlus HIGH-PERFORMANCE -
dc.subject.keywordPlus MOBILITY -
dc.subject.keywordPlus Optics -
dc.subject.keywordPlus P-CHANNEL -
dc.subject.keywordPlus PALLADIUM -
dc.subject.keywordPlus Priority Journal -
dc.subject.keywordPlus Pyrrole Derivative -
dc.subject.keywordPlus SemICONDUCTOR -
dc.subject.keywordPlus SENSITIZED SOLAR-CELLS -
dc.subject.keywordPlus SMALL-MOLECULE -
dc.subject.keywordPlus SOLID-STATE PROPERTIES -
dc.subject.keywordPlus Synthesis -
dc.subject.keywordPlus Thermogravimetry -
dc.subject.keywordPlus Thermostability -
dc.subject.keywordPlus Ultraviolet Spectroscopy -
dc.subject.keywordPlus Unclassified Drug -
dc.subject.keywordPlus X Ray Diffraction -
dc.citation.endPage 392 -
dc.citation.number 1 -
dc.citation.startPage 385 -
dc.citation.title New Journal of Chemistry -
dc.citation.volume 40 -
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ETC 1. Journal Articles
Center for Core Research Facilities 1. Journal Articles

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