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4-Acryloyl-1,2,2,6,6-pentamethyl-piperidinol (APMP) is a reactive hindered amine that prolongs the service life of the polymeric materials and exhibits high stability, good resistance to extraction, and low toxicity. In this paper, a photoinduced free radical copolymerization of APMP and methyl methacrylate (MMA) is accomplished at ambient temperature in solution. APMP plays a key role in the copolymerization, owing to the nitroxides generated in situ from the moiety of 1,2,2,6,6-pentamethyl-piperidine under UV irradiation, and mediates the copolymerization, which is confirmed by the linear kinetics. With the increment of initial monomer feed ratios of APMP/MMA, both the copolymerization rate and the average molecular weight increase. According to the reactivity ratios from the extended Kelen-Tüdos (KT) method at high conversion by 1H NMR spectroscopy, a nonlinear model is established and the sequential distribution in the copolymers is also investigated. The dispersion of APMP units is regulated by the feed ratios and reactivity ratios

Photoinduced Copolymerization of APMP-MMA: The Role of Reactive Hindered Amine APMP