pH-responsive and antimicrobial polymers were synthesized by photoinduced electron transfer-reversible addition-fragmentation chain transfer (PET-RAFT) polymerization under blue light (λmax = 485 nm) using a scalable continuous flow method. The effect of pendant alkylamino groups with different alkyl substituents on methacrylate monomers under blue light is investigated in the absence of a tertiary alkylamine reagent and in the presence of cyanopentanoic acid dithiobenzoate and 4-cyano-4-(dodecylsulfanylthiocarbonyl) sulfanylpentanoic acid as RAFT agents. The rate of polymerization is found to vary with the size of the alkyl chain and with the tertiary, secondary, or quaternary nature of the amino group. The ability of pendant alkylamino groups to transfer electrons to the photocatalyst is shown using cyclic voltammetry and fluorescence quenching experiments; the tendency to suppress dye aggregation is observed using UV–vis spectroscopy; and the rates of polymerization could be correlated with the trend in these results. The mechanism of polymerization is proposed to follow a reductive or oxidative electron transfer pathway depending on the nature of the pendant group. Statistical and diblock copolymers with 2-hydroxyethyl methacrylate are synthesized in batch and continuous flow processes with a comparative study of kinetics in the two methods. The synthesis of high-molecular-weight homopolymer (55,000 g/mol) and statistical copolymer (85,000 g/mol) of N,N-diisopropylaminoethyl methacrylate is shown in continuous flow. The solution self-assembly of diblock copolymers is studied, and the pH-responsive morphology change leading to disassembly is shown. The antimicrobial properties of polymers with a quaternary ammonium pendant group are evaluated. The thermal degradation of statistical copolymers is analyzed.
Patil et al. (Thu,) studied this question.