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A Supramolecular Approach to Metal Ion Sensing: Cystine-based Designer Systems for Cu2+, Hg2+, Cd2+ and Pb2+ Sensing

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dc.contributor.author Kumar, P P P
dc.contributor.author Suresh, C H
dc.contributor.author Haridas, V
dc.date.accessioned 2024-02-29T09:54:05Z
dc.date.available 2024-02-29T09:54:05Z
dc.date.issued 2015
dc.identifier.citation RSC Advances;5(11):7842-7847 en_US
dc.identifier.uri https://doi.org/10.1039/c4ra14389b
dc.identifier.uri http://localhost:8080/xmlui/handle/123456789/4792
dc.description.abstract We have synthesized two cystine containing molecules S1 (pyrene-labelled) and S2 (tryptophan-labelled) and demonstrated that the former can detect Cu2+, and the latter can detect Hg2+ in acetonitrile. The 1 : 1 mixture of S1 and S2 forms a heterodimeric system S1 : S2, which was confirmed by mass spectrometric, UV-Visible and fluorescence spectroscopic studies. Additional proof for the formation of S1 : S2 came from 1H NMR, CD, ITC, ultramicroscopic and computational studies. The supramolecularly assembled S1 : S2 detects Pb2+ in nanomolar levels. A control compound S3 containing tryptophan and pyrene units showed totally different binding properties compared to S1, S2 and S1 : S2. DFT studies on S1 : S2 establish that S1 in S1 : S2 adopts an extended conformation, thereby keeping the pyrene units proximal to the indole moiety of S2 for energy transfer. The binding of Pb2+ with S1 : S2 brings the two pyrene units into proximity resulting in a folded structure and the formation of the excimer. These results clearly demonstrate a hitherto unknown and unexpected organization of two fluorescent molecules leading to a new supramolecular system capable of Pb2+ detection. en_US
dc.language.iso en en_US
dc.publisher Royal society of chemistry en_US
dc.subject ion sensing en_US
dc.subject Cu2+, Hg2+, Cd2+ and Pb2+ en_US
dc.title A Supramolecular Approach to Metal Ion Sensing: Cystine-based Designer Systems for Cu2+, Hg2+, Cd2+ and Pb2+ Sensing en_US
dc.type Article en_US


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