Abstract
The photoinitiated copper(I) catalyzed azide-alkyne cycloaddition (photo-CuAAC) is a 'click' reaction that enables spatially and temporally controlled polymerizations. The solvent-less photopolymerization of multi-functional azide and cationic alkyne monomers results in the rapid formation of a charged polymer network. Full conversion of these monomers is achieved within 30 minutes under mild, blue-light irradiation conditions (470 nm light at 30 mW/cm(2)). The modulus of the material is readily tuned by controlling the ratio of di- and tri-functional alkyne monomers. Facile exchange of the hydrophobic bistriflimide counterion for a hydroxide anion yields an ion conductive polymer network with photopatternable charged regions. The spatiotemporal nature of the ionic photo-CuAAC reaction coupled with the chemical stability and mechanical flexibility suggests this chemistry is a facile and novel approach for ion-containing material synthesis (e.g., alkaline fuel cells components).