ABSTRACT
We demonstrated the photoredox catalytic performances of fluorescein derivatives, bearing heavy halogen atoms (Br or I) on a benzoic acid group, using photoinitiated free-radical polymerization. 4,5,6,7-Tetrabromofluorescein and 4,5,6,7-tetraiodofluorescein were used as visible-light-photoredox catalysts to initiate polymerization of poly(ethylene glycol) diacrylate and N-vinylpyrrolidone in the presence of triethanolamine under aerobic conditions. Their photocatalytic performances were evaluated by the hydrogelation of photopolymerization both on the surface of an agarose film and in a liquid solution. The polymerization degree increased considerably in the following order: tetraiodofluorescein
