Full metadata record
DC Field | Value | Language |
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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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