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Cited 393 time in webofscience Cited 394 time in scopus
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dc.contributor.authorJun, ME-
dc.contributor.authorRoy, B-
dc.contributor.authorAhn, KH-
dc.date.accessioned2015-06-25T01:43:08Z-
dc.date.available2015-06-25T01:43:08Z-
dc.date.created2011-08-11-
dc.date.issued2011-01-
dc.identifier.issn1359-7345-
dc.identifier.other2015-OAK-0000023958en_US
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/9990-
dc.description.abstractChemical probes are valuable tools for the investigation of biochemical processes, diagnosis of disease markers, detection of hazardous compounds, and other purposes. Therefore, the development of chemical probes continues to grow through various approaches with different disciplines and design strategies. Fluorescent probes have received much attention because they are sensitive and easy-to-operate, in general. To realize desired selectivity toward a given analyte, the recognition site of a fluorescent probe is designed in such a way to maximize the binding interactions, usually through weak molecular forces such as hydrogen bonding, toward the analyte over other competing ones. In addition to such a supramolecular approach, the development of fluorescent probes that sense analytes through chemical reactions has witnessed its usefulness for achieving high selectivity, in many cases, superior to that obtainable by the supramolecular approach. Creative incorporations of the reactive groups to latent fluorophores have provided novel chemical probes for various analytes. In this feature article, we overview the recent progress in the development of turn-on fluorescent probes that are operating through chemical reactions triggered by target analytes. Various chemical reactions have been implemented in the development of many reactive probes with very high selectivity and sensitivity toward target analytes. A major emphasis has been focused on the type of chemical reactions utilized, with the hope that further explorations can be made with new chemical reactions to develop reactive probes useful for various applications.-
dc.description.statementofresponsibilityopenen_US
dc.languageEnglish-
dc.publisherROYAL SOC CHEMISTRY-
dc.relation.isPartOfCHEMICAL COMMUNICATIONS-
dc.rightsBY_NC_NDen_US
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/2.0/kren_US
dc.titleTurn-on" fluorescent sensing with "reactive" probes-
dc.typeArticle-
dc.contributor.college화학과en_US
dc.identifier.doi10.1039/C1CC00014D-
dc.author.googleJun, MEen_US
dc.author.googleRoy, Ben_US
dc.author.googleAhn, KHen_US
dc.relation.volume47en_US
dc.relation.issue27en_US
dc.relation.startpage7583en_US
dc.relation.lastpage7601en_US
dc.contributor.id10087916en_US
dc.relation.journalCHEMICAL COMMUNICATIONSen_US
dc.relation.indexSCI급, SCOPUS 등재논문en_US
dc.relation.sciSCIen_US
dc.collections.nameJournal Papersen_US
dc.type.rimsART-
dc.identifier.bibliographicCitationCHEMICAL COMMUNICATIONS, v.47, no.27, pp.7583 - 7601-
dc.identifier.wosid000292113700003-
dc.date.tcdate2019-01-01-
dc.citation.endPage7601-
dc.citation.number27-
dc.citation.startPage7583-
dc.citation.titleCHEMICAL COMMUNICATIONS-
dc.citation.volume47-
dc.contributor.affiliatedAuthorAhn, KH-
dc.identifier.scopusid2-s2.0-79959790583-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc288-
dc.description.scptc282*
dc.date.scptcdate2018-10-274*
dc.type.docTypeArticle-
dc.subject.keywordPlusPHOTOINDUCED ELECTRON-TRANSFER-
dc.subject.keywordPlusRHODAMINE-BASED FLUORESCENT-
dc.subject.keywordPlusIMAGING HYDROGEN-PEROXIDE-
dc.subject.keywordPlusNITRIC-OXIDE-
dc.subject.keywordPlusSELECTIVE CHEMODOSIMETERS-
dc.subject.keywordPlusFLUOROGENIC REAGENTS-
dc.subject.keywordPlusFLUOROMETRIC ASSAY-
dc.subject.keywordPlusRATIONAL DESIGN-
dc.subject.keywordPlusBORONIC ACID-
dc.subject.keywordPlusCYANIDE-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-

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안교한AHN, KYO HAN
Dept of Chemistry
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