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A colorimetric chemosensor for distinct color change with (E)-2-(1-(3-aminophenyl)ethylideneamino)benzenethiol to detect Cu2+ in real water samples

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dc.contributor.authorPatil, Nilima-
dc.contributor.authorDhake, R. B.-
dc.contributor.authorPhalak, Raju-
dc.contributor.authorFegade, Umesh-
dc.contributor.authorInamuddin-
dc.contributor.authorNaushad, Mu.-
dc.contributor.authorBathula, Chinna-
dc.contributor.authorKanchi, Suvardhan-
dc.contributor.authorGovender, Krishna-
dc.date.accessioned2024-08-08T10:01:13Z-
dc.date.available2024-08-08T10:01:13Z-
dc.date.issued2023-08-
dc.identifier.issn0910-6340-
dc.identifier.issn1348-2246-
dc.identifier.urihttps://scholarworks.dongguk.edu/handle/sw.dongguk/21170-
dc.description.abstractThe study reports the synthesis of chemosensor (E)-2-(1-(3-aminophenyl)ethylideneamino)benzenethiol (C1), a highly sensitive, colorimetric metal probe that shows distinct selectivity for the detection of Cu2+ ion in various real water samples. Upon complexation with Cu2+ in CH3OH/H2O (60:40 v/v) (aqueous methanol), the C1 demonstrate significant enhancement in the absorption at 250 nm and 300 nm with a color change from light yellow to brown which was visualized using naked-eye. Therefore, these properties make C1 as an effective candidate for on-site Cu2+ ions detection. The emission spectrum of C1 illustrated "TURN-ON" recognition of Cu2+ with a limit of detection (LOD) of 46 nM. Furthermore, Density Functional Theory (DFT) calculations were performed to better understand the interactions between C1 and Cu2+. The obtained results suggested that the electron clouds present around the -NH2 in nitrogen and sulfur in -SH play a pivotal role in the formation of a stable complex. The computational results were in good agreement with the experimental UV-visible spectrometry results.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherSPRINGER NATURE-
dc.titleA colorimetric chemosensor for distinct color change with (E)-2-(1-(3-aminophenyl)ethylideneamino)benzenethiol to detect Cu2+ in real water samples-
dc.typeArticle-
dc.publisher.location영국-
dc.identifier.doi10.1007/s44211-023-00355-z-
dc.identifier.scopusid2-s2.0-85160933423-
dc.identifier.wosid001002724900001-
dc.identifier.bibliographicCitationAnalytical Sciences, v.39, no.8, pp 1413 - 1423-
dc.citation.titleAnalytical Sciences-
dc.citation.volume39-
dc.citation.number8-
dc.citation.startPage1413-
dc.citation.endPage1423-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Analytical-
dc.subject.keywordPlusFLUORESCENCE PROBE-
dc.subject.keywordPlusLIVING CELLS-
dc.subject.keywordPlusSOFT ACIDS-
dc.subject.keywordPlusCOPPER-
dc.subject.keywordPlusRECEPTOR-
dc.subject.keywordPlusSENSOR-
dc.subject.keywordPlusCATION-
dc.subject.keywordPlusNI2+-
dc.subject.keywordPlusRECOGNITION-
dc.subject.keywordPlusPYRENE-
dc.subject.keywordAuthorColorimetry-
dc.subject.keywordAuthorChemosensor-
dc.subject.keywordAuthorSchiff base-
dc.subject.keywordAuthorWater samples-
dc.subject.keywordAuthorDFT studies-
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College of Engineering (Department of Electronics and Electrical Engineering)
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