Efficient Conversion of Inert Nitriles to Multifunctional Poly(5-amino-1,2,3-triazole)s via Regioselective Click Polymerization with Azide Monomers under Ambient Conditions

Nitrile compounds are abundant, stable, cheap, and readily available natural and chemical industrial sources. However, the efficient conversion of nitrile monomers to functional polymers is mostly limited due to their inert reactivity, and developing efficient polymerizations based on nitrile monomers under very mild conditions is still a big challenge. In this work, a facile and powerful base-catalyzed acetonitrile-azide click polymerization was successfully established under ambient conditions. This polymerization also enjoys the merits of short reaction time (15 min), 100% atom economy, transition-metal-free catalyst system, and regioselectivity. A series of poly(5-amino-1,2,3-triazole)s (PATAs) with high weight-average molecular weights (M_w, up to 204,000) were produced in excellent yields (up to 99%). The PATAs containing tetraphenylethene (TPE) moieties exhibit unique aggregation-induced emission (AIE) characteristics, which could be used to sensitively detect Fe(III) ions with a low limit of detection (1.205 × 10^-7 M) and to specifically image lysosomes of living cells. Notably, PATAs could be facilely post-modified due to their containing primary amino groups in the polymer chains even through a one-pot tandem reaction. Thus, this work not only establishes a new powerful click polymerization to convert stable nitriles but also generates a series of PATAs with versatile properties for diverse applications.