Fluorescence Control on Panchromatic Spectra via C-Alkylation on Arylated Quinoxalines
DC Field | Value | Language |
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dc.contributor.author | Son, Ho-Jin | - |
dc.contributor.author | Han, Won-Sik | - |
dc.contributor.author | You, Dae-Hwan | - |
dc.contributor.author | Min, Kyoung-Tae | - |
dc.contributor.author | Kwon, Soon-Nam | - |
dc.contributor.author | Ko, Jaejung | - |
dc.contributor.author | Kang, Sang Ook | - |
dc.date.accessioned | 2021-09-08T18:04:20Z | - |
dc.date.available | 2021-09-08T18:04:20Z | - |
dc.date.created | 2021-06-10 | - |
dc.date.issued | 2009-04-17 | - |
dc.identifier.issn | 0022-3263 | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/120233 | - |
dc.description.abstract | A coherent green fluorescence was obtained by butylation at the 2-position of panchromatic 2,3-diaryl-5,8-diarylquinoxalines (2) to give corresponding 2-butyl-2,3-diaryl-5,8diaryl-1H-quinoxalines (3). Full color quinoxaline derivatives (2) were prepared from electronic modification at either the 2,3- or 5,8-positions at the peripheral ArX group or X group (X = -H, -OMe, -NPh2, -NMe2, -NMePh) of the quinoxalines. 2-Butylation converted one imine unit of the pyrazine ring to an amine group, which effectively altered the electron donor and acceptor functions to produce a coherent green fluorescence. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.subject | LIGHT-EMITTING-DIODES | - |
dc.subject | CHARGE-TRANSFER PHOTOPHYSICS | - |
dc.subject | ELECTRON-TRANSPORT MATERIALS | - |
dc.subject | ELECTROLUMINESCENT MATERIALS | - |
dc.subject | OPTOELECTRONIC APPLICATIONS | - |
dc.subject | DERIVATIVES | - |
dc.subject | MOLECULES | - |
dc.subject | DEVICES | - |
dc.subject | CHROMOPHORES | - |
dc.subject | EMISSION | - |
dc.title | Fluorescence Control on Panchromatic Spectra via C-Alkylation on Arylated Quinoxalines | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Ko, Jaejung | - |
dc.contributor.affiliatedAuthor | Kang, Sang Ook | - |
dc.identifier.doi | 10.1021/jo9002147 | - |
dc.identifier.scopusid | 2-s2.0-65249106212 | - |
dc.identifier.wosid | 000265073700039 | - |
dc.identifier.bibliographicCitation | JOURNAL OF ORGANIC CHEMISTRY, v.74, no.8, pp.3175 - 3178 | - |
dc.relation.isPartOf | JOURNAL OF ORGANIC CHEMISTRY | - |
dc.citation.title | JOURNAL OF ORGANIC CHEMISTRY | - |
dc.citation.volume | 74 | - |
dc.citation.number | 8 | - |
dc.citation.startPage | 3175 | - |
dc.citation.endPage | 3178 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Chemistry | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |
dc.subject.keywordPlus | LIGHT-EMITTING-DIODES | - |
dc.subject.keywordPlus | CHARGE-TRANSFER PHOTOPHYSICS | - |
dc.subject.keywordPlus | ELECTRON-TRANSPORT MATERIALS | - |
dc.subject.keywordPlus | ELECTROLUMINESCENT MATERIALS | - |
dc.subject.keywordPlus | OPTOELECTRONIC APPLICATIONS | - |
dc.subject.keywordPlus | DERIVATIVES | - |
dc.subject.keywordPlus | MOLECULES | - |
dc.subject.keywordPlus | DEVICES | - |
dc.subject.keywordPlus | CHROMOPHORES | - |
dc.subject.keywordPlus | EMISSION | - |
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