Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.polymer.2006.05.045
Title: A bipyridine-containing water-soluble conjugated polymer: Highly efficient fluorescence chemosensor for convenient transition metal ion detection in aqueous solution
Authors: Chen, Y.
Fan, Q.-L.
Wang, P.
Zhang, B.
Huang, Y.-Q.
Zhang, G.-W.
Lu, X.-M.
Chan, H.S.O. 
Huang, W. 
Keywords: Bipyridyl
Fluorescence chemosensor
Water-soluble conjugated polymer
Issue Date: 12-Jul-2006
Citation: Chen, Y., Fan, Q.-L., Wang, P., Zhang, B., Huang, Y.-Q., Zhang, G.-W., Lu, X.-M., Chan, H.S.O., Huang, W. (2006-07-12). A bipyridine-containing water-soluble conjugated polymer: Highly efficient fluorescence chemosensor for convenient transition metal ion detection in aqueous solution. Polymer 47 (15) : 5228-5232. ScholarBank@NUS Repository. https://doi.org/10.1016/j.polymer.2006.05.045
Abstract: A novel sulfonato-functionalized water-soluble conjugated polymer (WSCP), which containing 2′2-bipyridine units as receptors for transition metal ions in the main chain was successfully synthesized by Sonogashira-coupling reaction for the first time. This polymer could easily dissolve in water (5 mg/mL) and some polar organic solvents such as methanol. Its fluorescence in aqueous solution can be completely quenched upon addition of transition metal ions. The Ksv of different transition metal ions in aqueous solution were much higher than previous reports in organic solutions and showed highest selectivity to Ni2+. These results opened opportunities for developing novel chemosensors by introducing selective fluorescent chromophore into the water-soluble conjugated backbone. © 2006 Elsevier Ltd. All rights reserved.
Source Title: Polymer
URI: http://scholarbank.nus.edu.sg/handle/10635/91841
ISSN: 00323861
DOI: 10.1016/j.polymer.2006.05.045
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.