View : 826 Download: 0

Full metadata record

DC Field Value Language
dc.contributor.author김성진*
dc.contributor.author김영미*
dc.contributor.author윤주영*
dc.contributor.authorK.M.K Swamy*
dc.date.accessioned2019-07-22T16:30:45Z-
dc.date.available2019-07-22T16:30:45Z-
dc.date.issued2019*
dc.identifier.issn0143-7208*
dc.identifier.otherOAK-25092*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/250149-
dc.description.abstractThe results of the current study show that fluoride and cyanide recognition by two naphthoimidazolium derivatives can be applied to CO2 sensing. Among various anions, only fluoride and cyanide promote changes in absorption and fluorescence wavelegnth maxima of the naphthoimidazolium derivative in CH3CN. The changes are attributed to (C–H)+—anion- ionic hydrogen bonding interactions between the conjugated imidazolium salts and these anions. Especially important is the observations that the fluorescence emission maxima of the naphthoimidazolium derivative at 465 nm undergo hysochromic shifts to 375 nm upon addition of fluoride and cyanide exclusively. The naphthoimidazolium derivatives undergo highly selective changes in their fluoerecence maximum from 465 nm to 375 nm upon addition of CN− even when 2% water is present in the CH3CN solution. Moreover, exposure of the solution of CN− activated naphthoimidazolium derivative to CO2 promotes a red shift of emission maximum back to 465 nm. The results demonstrate that the naphthoimidazolium derivatives can be utilized for anion activated ratiometric sensing of CO2. © 2019*
dc.languageEnglish*
dc.publisherElsevier Ltd*
dc.subjectcarbon dioxide sensor*
dc.subjectCyanide selective fluorescent probe*
dc.subjectFluoride selective fluorescent probe*
dc.subjectImidazolium receptor for anions*
dc.subjectRatiomertic fluorescent sensor*
dc.titleNaphthoimidazolium based ratiometric fluorescent probes for F− and CN−, and anion-activated CO2 sensing*
dc.typeArticle*
dc.relation.volume171*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.journaltitleDyes and Pigments*
dc.identifier.doi10.1016/j.dyepig.2019.107679*
dc.identifier.wosidWOS:000484870700038*
dc.identifier.scopusid2-s2.0-85068483865*
dc.author.googleKwon N.*
dc.author.googleBaek G.*
dc.author.googleSwamy K.M.K.*
dc.author.googleLee M.*
dc.author.googleXu Q.*
dc.author.googleKim Y.*
dc.author.googleKim S.-J.*
dc.author.googleYoon J.*
dc.contributor.scopusid김성진(56812714700)*
dc.contributor.scopusid김영미(57207443602)*
dc.contributor.scopusid윤주영(7403587371)*
dc.contributor.scopusidK.M.K Swamy(8384468700)*
dc.date.modifydate20240301081003*
Appears in Collections:
자연과학대학 > 화학·나노과학전공 > Journal papers
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML


qrcode

BROWSE