Customizing STEM organogels using PET-RAFT polymerization

Abstract

Photoinduced electron/energy transfer (PET) reversible addition-fragmentation chain transfer (RAFT) polymerization results in more uniform polymer networks compared to networks synthesized by thermally initiated RAFT polymerizations. However, how PET-RAFT polymerizations affect molecular weight control and physical properties during parent-to-daughter block copolymer network synthesis is unclear. Herein, we synthesized a structurally tailored and engineered macromolecular (STEM) organogel composed of poly(methyl acrylate) and a degradable crosslinker. Chain extensions on the STEM organogel were performed using PET-RAFT polymerization of either methyl acrylate (MA) or N,N-dimethylacrylamide (DMA) with or without additional crosslinker. We found that physical properties were dependent on monomer composition and crosslinking. The swelling ratios of the diblock networks were similar in DMAc. Conversely, swelling ratios in water increased by 430% for networks extended with MA and 5200% for networks extended with DMA compared to the parent organogels. Rheological analysis showed a tunable modulus from 1000-4000 Pa. However, size exclusion chromatography analysis of the degraded gels revealed that the PET-RAFT polymerization chain extension yielded disperse block copolymers with poor control over the molecular weight. These results indicate that PET-RAFT polymerizations can be used to expand organogel networks to block copolymer networks to modulate physical properties, but control over the chain extension polymerization is lost. Looking forward, this report points to opportunities to gain control over PET-RAFT block copolymer network synthesis via secondary reversible deactivation pathways. PET-RAFT polymerization was used to modify STEM organogels, while degradable linkers enabled the characterization of the resulting block copolymers.