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dc.contributor.author김영미*
dc.date.accessioned2018-11-21T16:30:39Z-
dc.date.available2018-11-21T16:30:39Z-
dc.date.issued2018*
dc.identifier.issn0143-7208*
dc.identifier.otherOAK-22212*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/246818-
dc.description.abstractTubular-shaped chromophores have great potential in chemical and material sciences. A naphthalene-containing macrocyclic diacetylene (MCDA-Naph) was synthesized to access covalently linked organic nanotubes (ONTs) through topochemical polymerization. Single crystal X-ray analysis revealed that MCDA-Naph adopts the desired tubular array with favorable molecular orientation. UV irradiation of the molecularly stacked MCDA-Naph resulted in 1,4-addition polymerization and the generation of conjugated ene-yne chromophores. Density functional theory (DFT) provided evidence for tubular polydiacetylene nanotubes. © 2018*
dc.description.sponsorshipSamsung*
dc.languageEnglish*
dc.publisherElsevier Ltd*
dc.subjectChromophore*
dc.subjectConjugated polymer*
dc.subjectMacrocyclic diacetylene*
dc.subjectPolydiacetylene*
dc.subjectTopochemical polymerization*
dc.titleTopochemical polymerization of macrocyclic diacetylene with a naphthalene moiety for a tubular-shaped polydiacetylene chromophore*
dc.typeArticle*
dc.relation.volume154*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage199*
dc.relation.lastpage204*
dc.relation.journaltitleDyes and Pigments*
dc.identifier.doi10.1016/j.dyepig.2018.02.039*
dc.identifier.wosidWOS:000432501000026*
dc.identifier.scopusid2-s2.0-85042940458*
dc.author.googleKantha C.*
dc.author.googleKim H.*
dc.author.googleKim Y.*
dc.author.googleHeo J.-M.*
dc.author.googleJoung J.F.*
dc.author.googlePark S.*
dc.author.googleKim J.-M.*
dc.contributor.scopusid김영미(57207443602)*
dc.date.modifydate20240301081003*
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자연과학대학 > 화학·나노과학전공 > Journal papers
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