Cu2+ Ion-Induced Self-Assembly of Pyrenylquinoline with a Pyrenyl Excimer Formation
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Jung, Hyo Sung | - |
dc.contributor.author | Park, Mirae | - |
dc.contributor.author | Han, Do Young | - |
dc.contributor.author | Kim, Eunmi | - |
dc.contributor.author | Lee, Chewook | - |
dc.contributor.author | Ham, Sihyun | - |
dc.contributor.author | Kim, Jong Seung | - |
dc.date.accessioned | 2021-09-08T14:51:37Z | - |
dc.date.available | 2021-09-08T14:51:37Z | - |
dc.date.created | 2021-06-10 | - |
dc.date.issued | 2009-08-06 | - |
dc.identifier.issn | 1523-7060 | - |
dc.identifier.uri | https://scholar.korea.ac.kr/handle/2021.sw.korea/119503 | - |
dc.description.abstract | Synthesis of a novel pyrene derivative sensor (1) and its intermolecular binding pattern to Cu2+ in CH3CN were investigated. Upon Cu2+ binding, the sensor exhibited a strong static excimer emission at 460 nm, along with a weak monomer emission at 388 nm. The excimer emission intensity induced by the Cu2+ ion declined as the spacer length between the pyrene and quinolinylamide unit increased. The Cu2+ ion-induced self-assembled pyrenyl excimer formation is rationalized by fluorescence experiments and theoretical DFT calculations. | - |
dc.language | English | - |
dc.language.iso | en | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.subject | SELECTIVE FLUORESCENT SENSOR | - |
dc.subject | TRANSITION-METAL IONS | - |
dc.subject | STATES | - |
dc.subject | FLUOROIONOPHORE | - |
dc.subject | COMPLEXATION | - |
dc.subject | CHEMOSENSORS | - |
dc.subject | RECOGNITION | - |
dc.subject | RATIOMETRY | - |
dc.subject | MOLECULES | - |
dc.subject | CHEMISTRY | - |
dc.title | Cu2+ Ion-Induced Self-Assembly of Pyrenylquinoline with a Pyrenyl Excimer Formation | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Kim, Jong Seung | - |
dc.identifier.doi | 10.1021/ol901221q | - |
dc.identifier.scopusid | 2-s2.0-68149089673 | - |
dc.identifier.wosid | 000268479900055 | - |
dc.identifier.bibliographicCitation | ORGANIC LETTERS, v.11, no.15, pp.3378 - 3381 | - |
dc.relation.isPartOf | ORGANIC LETTERS | - |
dc.citation.title | ORGANIC LETTERS | - |
dc.citation.volume | 11 | - |
dc.citation.number | 15 | - |
dc.citation.startPage | 3378 | - |
dc.citation.endPage | 3381 | - |
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 | SELECTIVE FLUORESCENT SENSOR | - |
dc.subject.keywordPlus | TRANSITION-METAL IONS | - |
dc.subject.keywordPlus | STATES | - |
dc.subject.keywordPlus | FLUOROIONOPHORE | - |
dc.subject.keywordPlus | COMPLEXATION | - |
dc.subject.keywordPlus | CHEMOSENSORS | - |
dc.subject.keywordPlus | RECOGNITION | - |
dc.subject.keywordPlus | RATIOMETRY | - |
dc.subject.keywordPlus | MOLECULES | - |
dc.subject.keywordPlus | CHEMISTRY | - |
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