Radical copolymerization, with various monomer feeds of phenyl vinylethylene carbonate (PVEC) and N-phenylmaleimide (PMI), successfully proceeded through selective vinyl and alternating polymerization to obtain copolymers having the maleimide unit in… Click to show full abstract
Radical copolymerization, with various monomer feeds of phenyl vinylethylene carbonate (PVEC) and N-phenylmaleimide (PMI), successfully proceeded through selective vinyl and alternating polymerization to obtain copolymers having the maleimide unit in the main-chain and the five-membered cyclic carbonate group in the side-chain. The structure of these copolymers was analyzed in detail using NMR, IR, and UV-Vis methods. The UV-Vis spectra supported the tautomerization of the maleimide unit based on the solvent effect and the alternating and/or homo sequence constructed depending on the monomer feeds. Furthermore, these copolymers exhibited sensitive and reversible color changes based on acid–base switching not only in solution but also in the solid-state. In particular, the color change in the solid-state occurred immediately after exposure to the amine vapor.
               
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