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DC Field | Value | Language |
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dc.citation.endPage | 392 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 385 | - |
dc.citation.title | NEW JOURNAL OF CHEMISTRY | - |
dc.citation.volume | 40 | - |
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.accessioned | 2023-12-22T00:11:40Z | - |
dc.date.available | 2023-12-22T00:11:40Z | - |
dc.date.created | 2020-03-17 | - |
dc.date.issued | 2016-01 | - |
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. | - |
dc.identifier.bibliographicCitation | NEW JOURNAL OF CHEMISTRY, v.40, no.1, pp.385 - 392 | - |
dc.identifier.doi | 10.1039/c5nj02631h | - |
dc.identifier.issn | 1144-0546 | - |
dc.identifier.scopusid | 2-s2.0-84953299104 | - |
dc.identifier.uri | https://scholarworks.unist.ac.kr/handle/201301/31594 | - |
dc.identifier.url | https://pubs.rsc.org/en/content/articlelanding/2016/nj/c5nj02631h#!divAbstract | - |
dc.identifier.wosid | 000367621300050 | - |
dc.language | 영어 | - |
dc.publisher | ROYAL SOC 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.description.isOpenAccess | FALSE | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.type.docType | Article | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | SENSITIZED SOLAR-CELLS | - |
dc.subject.keywordPlus | FIELD-EFFECT TRANSISTORS | - |
dc.subject.keywordPlus | SOLID-STATE PROPERTIES | - |
dc.subject.keywordPlus | SMALL-MOLECULE | - |
dc.subject.keywordPlus | HIGH-PERFORMANCE | - |
dc.subject.keywordPlus | CHARGE-TRANSPORT | - |
dc.subject.keywordPlus | P-CHANNEL | - |
dc.subject.keywordPlus | MOBILITY | - |
dc.subject.keywordPlus | SEMICONDUCTOR | - |
dc.subject.keywordPlus | CRYSTALLINITY | - |
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