Abstract
The oxygen inhibition and migration of micromolecules which stem from photoinitiators (PIs) remain two critical challenges to address in radical photocuring. In this work, we reported a one-step ternary copolymerization strategy to construct a one-component macromolecular photoinitiator (PPI) using polymerizable thioxanthone (TX), amine (N), and fluorinated alkane (F) as monomers. Then, we utilize the low surface energy of F unit and macromolecular skeleton to reduce oxygen inhibition and migration. Compared to micromolecule TX, PPI also exhibits a broad absorption in the 250-430 nm range, and a higher molar extinction coefficient. The effects of the TX, N, and F component ratios on the photoinitiation efficiency of PPI were systematically investigated, and the photopolymerization kinetics revealed that the increased content of F unit can eliminate the oxygen inhibition of PPI. As a result, PPI demonstrates the more superior photoinitiation efficiency compared to the traditional TX/N two-component macromolecule photoinitiation system. Migration experiments indicated that there is a 60% reduction in the migration rate for PPI compared to the TX/N photoinitiation system. This work provides an effective strategy to address oxygen inhibition and micromolecule migration issues in radical photocuring, showing potential applications in food and pharmaceutical packaging fields.