Fluorene‐based conjugated polymer with tethered thymines: click postpolymerization synthesis and optical response to mercury(II)

A kind of fluorene‐based conjugated polymer with tethered thymine (T) groups {poly[(9,9‐dioctyl)‐2,7‐fluorene‐{9,9‐dioctyl‐4–1,2,3‐triazol‐[5‐(hydroxymethyl)tetrahydrofuran‐2‐yl]‐5‐methylpyrimidine‐2,4(1H,3H)‐dione}‐2,7‐fluorene]‐ co ‐[(9,9‐dioctyl)‐2,7‐fluorene‐4,7‐bis(5‐thiophen‐2‐yl)benzo‐2,1,3‐thiadiazole] ( P‐3 )} was successfully synthesized by a Cu(I)‐catalyzed click reaction between the acetylene‐substituted polymer precursor {poly[(9,9‐dioctyl)‐2,7‐fluorene‐(9,9‐dioctyl‐4‐phenylacetylene fluorene)]‐ co ‐[(9,9‐dioctyl)‐2,7‐fluorene‐4,7‐bis(5‐thiophen‐2‐yl)benzo‐2,1,3‐thiadiazole]} and 3′‐azido‐3′‐deoxythymidine. The chemical structures of the intermediates and target polymer were verified by Fourier transform infrared spectroscopy and 1 H‐NMR analyses. The specific binding with Hg 2+ of P‐3 was corroborated by ultraviolet–visible spectroscopy and photoluminescence analyses against other metal ions. The results show that P‐3 possessed selectivity and sensitivity toward Hg 2+ . Around 77% of photoluminescence intensity of P‐3 was quenched when the concentration of Hg 2+ reached 7.7 × 10 −4 M and with a detection limit in the range of about 4.8 μ M . A comparison experiment suggested that a synergic effect of the tethered T and S atoms interrelated with Hg 2+ existed in P‐3 . Most of the fluorescence intensity of P‐3 was recovered upon the addition of iodide anions to the P‐3 /Hg 2+ complex; this suggested that P‐3 could be used as a potential reversible optical Hg 2+ probe. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013