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A molecular recognition platform for the simultaneous sensing of diverse chemical weapons

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dc.contributor.authorZeng, Lintao-
dc.contributor.authorChen, Tianhong-
dc.contributor.authorZhu, Beitong-
dc.contributor.authorKoo, Seyoung-
dc.contributor.authorTang, Yonghe-
dc.contributor.authorLin, Weiying-
dc.contributor.authorJames, Tony D.-
dc.contributor.authorKim, Jong Seung-
dc.date.accessioned2024-09-23T08:30:20Z-
dc.date.available2024-09-23T08:30:20Z-
dc.date.issued2022-04-
dc.identifier.issn2041-6520-
dc.identifier.issn2041-6539-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/120544-
dc.description.abstractChemical warfare agents (CWAs) such as phosgene and nerve agents pose serious threats to our lives and public security, but no tools can simultaneously screen multiple CWAs in seconds. Here, we rationally designed a robust sensing platform based on 8-cyclohexanyldiamino-BODIPY (BODIPY-DCH) to monitor diverse CWAs in different emission channels. Trans-cyclohexanyldiamine as the reactive site provides optimal geometry and high reactivity, allowing trans-BODIPY-DCH to detect CWAs with a quick response and high sensitivity, while cis-BODIPY-DCH has much weaker reactivity to CWAs due to intramolecular H-bonding. Upon reaction with phosgene, trans-BODIPY-DCH was rapidly converted to imidazolone BODIPY (<3 s), triggering green fluorescence with good sensitivity (LOD = 0.52 nM). trans-BODIPY-DCH coupled with nerve agent mimics, affording a blue fluorescent 8-amino-BODIPY tautomer. Furthermore, a portable test kit using trans-BODIPY-DCH displayed an instant response and low detection limits for multiple CWAs. This platform enables rapid and highly sensitive visual screening of various CWAs. © 2022 The Royal Society of Chemistry-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherRoyal Society of Chemistry-
dc.titleA molecular recognition platform for the simultaneous sensing of diverse chemical weapons-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1039/d2sc00299j-
dc.identifier.scopusid2-s2.0-85127326597-
dc.identifier.wosid000772119000001-
dc.identifier.bibliographicCitationChemical Science, v.13, no.16, pp 4523 - 4532-
dc.citation.titleChemical Science-
dc.citation.volume13-
dc.citation.number16-
dc.citation.startPage4523-
dc.citation.endPage4532-
dc.type.docType정기학술지(Article(Perspective Article포함))-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusFLUORESCENT SENSOR-
dc.subject.keywordPlusWARFARE AGENTS-
dc.subject.keywordPlusSULFUR MUSTARD-
dc.subject.keywordPlusLUNG INJURY-
dc.subject.keywordPlusTURN-ON-
dc.subject.keywordPlusPHOSGENE-
dc.subject.keywordPlusPROBE-
dc.subject.keywordPlusSARIN-
dc.subject.keywordPlusCHLORIDE-
dc.identifier.urlhttps://pubs.rsc.org/en/content/articlelanding/2022/sc/d2sc00299j-
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ERICA 공학대학 (ERICA 에너지바이오학과)
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