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 |