Please use this identifier to cite or link to this item: https://doi.org/10.1002/asia.200700294
Title: Synthesis and characterization of a water-soluble carboxylated polyfluorene and its fluorescence quenching by cationic quenchers and proteins
Authors: Zhang, Y. 
Liu, B. 
Cao, Y.
Keywords: Biosensors
Fluorescence quenching
Polyfluorenes
Polymers
Proteins
Issue Date: 7-Apr-2008
Citation: Zhang, Y., Liu, B., Cao, Y. (2008-04-07). Synthesis and characterization of a water-soluble carboxylated polyfluorene and its fluorescence quenching by cationic quenchers and proteins. Chemistry - An Asian Journal 3 (4) : 739-745. ScholarBank@NUS Repository. https://doi.org/10.1002/asia.200700294
Abstract: We have developed a new intermediate monomer, 2,7-[bis(4,4,5,5-tetramethyl- 1,3,2-dioxaborolan-2-yl)-9,9-bis(3-(tert-butyl propanoate))]fluorene, that allows the easy synthesis of water-soluble carboxylated polyfluorenes. As an example, poly[9,9′-bis(3″-propanoate)fluoren-2,7-yl] sodium salt was synthesized by the Suzuki coupling reaction, and the properties of the polymer were studied in aqueous solutions of different pH. Fluorescence quenching of the polymer by different cationic quenchers (MV2+, MV4+, and NO2MV2+; MV=methyl viologen) was studied, and the quenching constants were found to be dependent on the charge and electron affinity of the quencher molecule and the pH of the medium. The largest quenching constant was observed to be 1.39×108M-1 for NO2MV2+ at pH 7. The change in polymer fluorescence upon interaction with different proteins was also studied. Strong fluorescence quenching of the polymer was observed in the presence of cytochrome c, whereas weak quenching was observed in the presence of myoglobin and bovine serum albumin. Lysozyme quenched the polymer emission at low protein concentrations, and the quenching became saturated at high protein concentrations. Under similar experimental conditions, the polymer showed improved quenching efficiencies toward cationic quenchers and a more selective response to proteins relative to other carboxylated conjugated polymers. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.
Source Title: Chemistry - An Asian Journal
URI: http://scholarbank.nus.edu.sg/handle/10635/90255
ISSN: 18614728
DOI: 10.1002/asia.200700294
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