A caveat to common hemicyanine dye components and their resolution

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dc.contributor.authorPark, Hyeon Jinko
dc.contributor.authorSong, Chang Wookko
dc.contributor.authorSarkar, Souravko
dc.contributor.authorJun, Yong Woongko
dc.contributor.authorReo, Ye Jinko
dc.contributor.authorDai, Mingchongko
dc.contributor.authorAhn, Kyo Hanko
dc.date.accessioned2023-05-03T07:00:54Z-
dc.date.available2023-05-03T07:00:54Z-
dc.date.created2023-05-03-
dc.date.created2023-05-03-
dc.date.created2023-05-03-
dc.date.issued2020-06-
dc.identifier.citationCHEMICAL COMMUNICATIONS, v.56, no.51, pp.7025 - 7028-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10203/306512-
dc.description.abstractNear-infrared-emitting hemicyanine dyes are widely used in activatable fluorescent probes for various biological analytes; however, they are chemically unstable and show photoinstability, as shown here with naphthalene-based hemicyanines containing a typical hemicyanine moiety, 2-indolium. These issues can be resolved with a 4-pyridinium derivative, which also has good two-photon imaging capability.-
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.titleA caveat to common hemicyanine dye components and their resolution-
dc.typeArticle-
dc.identifier.wosid000542898200023-
dc.identifier.scopusid2-s2.0-85087110761-
dc.type.rimsART-
dc.citation.volume56-
dc.citation.issue51-
dc.citation.beginningpage7025-
dc.citation.endingpage7028-
dc.citation.publicationnameCHEMICAL COMMUNICATIONS-
dc.identifier.doi10.1039/d0cc01833c-
dc.contributor.localauthorJun, Yong Woong-
dc.contributor.nonIdAuthorPark, Hyeon Jin-
dc.contributor.nonIdAuthorSong, Chang Wook-
dc.contributor.nonIdAuthorSarkar, Sourav-
dc.contributor.nonIdAuthorReo, Ye Jin-
dc.contributor.nonIdAuthorDai, Mingchong-
dc.contributor.nonIdAuthorAhn, Kyo Han-
dc.description.isOpenAccessN-
dc.type.journalArticleArticle-
dc.subject.keywordPlusRATIOMETRIC FLUORESCENT-PROBE-
dc.subject.keywordPlusSO2 DERIVATIVES BISULFITE-
dc.subject.keywordPlusRAPID DETECTION-
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