Chaiprasert T.Chanmungkalakul S.Liu Y.Bureerug T.Silpcharu K.Unno M.Xiaogang L.Ervithayasuporn V.Chang Y.T.Rashatasakhon P.Mahidol University2023-06-182023-06-182022-12-01Dyes and Pigments Vol.208 (2022)01437208https://repository.li.mahidol.ac.th/handle/20.500.14594/84031Two 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.Chemical EngineeringArticleSCOPUS10.1016/j.dyepig.2022.1107932-s2.0-8513931549918733743