Synthesis, Thermoresponsive Behavior, and Catalytic Properties of Amphiphilic Diblock Copolymers of N-Vinylcaprolactam and N-Vinylimidazole

Thermoresponsive diblock copolymers (DCs) were prepared by two-stage reversible addition-fragmentation chain transfer/macromolecular design by interchange of xanthate (RAFT/MADIX) polymerization of N-vinylcaprolactam and N-vinylimidazole (VI). The poly(N-vinylcaprolactam) (PVCL) blocks were first synthesized and used as macro-chain transfer agent in VI polymerization. The temperature behavior of PVCL and DCs in aqueous media has been studied by static and dynamic light scattering. It has been shown that the phase separation temperature of both PVCLs and DCs depends on the length of the PVCL chain and the composition of aqueous solvent. The temperature range above the PVCL theta temperature and below the cloud point is characterized by the conformational rearrangements leading to the formation of mesoglobules. The study of catalytic activity of DCs in the hydrolysis reaction of p-nitrophenyl propionate has shown that their activity substantially increases in this transitional temperature region owing to the formation of highly developed hydrophilic-hydrophobic interfaces inside the mesoglobules.

Automated summary

Thermoresponsive diblock copolymers were prepared by reversible addition-fragmentation chain transfer/macromolecular design and studied for their temperature behavior and catalytic activity. The phase separation temperature of the copolymers depended on the length of the PVCL chain and the composition of the solvent, and the formation of hydrophilic-hydrophobic interfaces inside mesoglobules enhanced catalytic activity.