Fluorescent Janus ring siloxanes for detection of Au(III) and L-cysteine
Two new all-cis pyrene-substituted cyclic tetrasiloxanes (JR-01 and JR-02) are synthesized and studied as selective metal ion sensors. Both compounds exhibit solvent- and concentration-dependent excimer fluorescence emission at 482 nm. They also show highly selective fluorescence quenching by Au(III...
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th-mahidol.840312023-06-18T23:53:45Z Fluorescent Janus ring siloxanes for detection of Au(III) and L-cysteine Chaiprasert T. Mahidol University Chemical Engineering Two new all-cis pyrene-substituted cyclic tetrasiloxanes (JR-01 and JR-02) are synthesized and studied as selective metal ion sensors. Both compounds exhibit solvent- and concentration-dependent excimer fluorescence emission at 482 nm. They also show highly selective fluorescence quenching by Au(III) ion with detection limits of 0.9 and 0.8 μM for JR-01 and JR-02, respectively. Data from the Stern-Volmer's plots at various temperatures, zetasizers, NMR, and UV–Vis spectroscopy indicate a plausible mechanism involving the formation of a non-emissive Au(III) complex. An application of JR-01 as Au(III) sensor in real water samples reveals a good sensing efficiency which is comparable to the analysis result from ICP-QMS. In addition, when an excess amount of L-cysteine is added to the JR-01/Au(III) mixture, the fluorescence signal is restored and the 1H NMR data suggests that JR-01 remains intact. As an extension of this study, we successfully demonstrate the detection of L-cysteine by fluorescence turn-on process using the JR-01/Au(III) mixture with a detection limit of 14.0 μM. 2023-06-18T16:53:45Z 2023-06-18T16:53:45Z 2022-12-01 Article Dyes and Pigments Vol.208 (2022) 10.1016/j.dyepig.2022.110793 18733743 01437208 2-s2.0-85139315499 https://repository.li.mahidol.ac.th/handle/123456789/84031 SCOPUS |
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Chemical Engineering Chaiprasert T. Fluorescent Janus ring siloxanes for detection of Au(III) and L-cysteine |
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Two new all-cis pyrene-substituted cyclic tetrasiloxanes (JR-01 and JR-02) are synthesized and studied as selective metal ion sensors. Both compounds exhibit solvent- and concentration-dependent excimer fluorescence emission at 482 nm. They also show highly selective fluorescence quenching by Au(III) ion with detection limits of 0.9 and 0.8 μM for JR-01 and JR-02, respectively. Data from the Stern-Volmer's plots at various temperatures, zetasizers, NMR, and UV–Vis spectroscopy indicate a plausible mechanism involving the formation of a non-emissive Au(III) complex. An application of JR-01 as Au(III) sensor in real water samples reveals a good sensing efficiency which is comparable to the analysis result from ICP-QMS. In addition, when an excess amount of L-cysteine is added to the JR-01/Au(III) mixture, the fluorescence signal is restored and the 1H NMR data suggests that JR-01 remains intact. As an extension of this study, we successfully demonstrate the detection of L-cysteine by fluorescence turn-on process using the JR-01/Au(III) mixture with a detection limit of 14.0 μM. |
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Mahidol University |
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Mahidol University Chaiprasert T. |
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Chaiprasert T. |
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Chaiprasert T. |
title |
Fluorescent Janus ring siloxanes for detection of Au(III) and L-cysteine |
title_short |
Fluorescent Janus ring siloxanes for detection of Au(III) and L-cysteine |
title_full |
Fluorescent Janus ring siloxanes for detection of Au(III) and L-cysteine |
title_fullStr |
Fluorescent Janus ring siloxanes for detection of Au(III) and L-cysteine |
title_full_unstemmed |
Fluorescent Janus ring siloxanes for detection of Au(III) and L-cysteine |
title_sort |
fluorescent janus ring siloxanes for detection of au(iii) and l-cysteine |
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2023 |
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https://repository.li.mahidol.ac.th/handle/123456789/84031 |
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