Hydrophilic polymer supports grafted by poly(ethylene glycol) derivatives via atom transfer radical polymerization

In this study, a newly structured hydrophilic polymer supports are prepared by the chemical modification (grafting) of the polystyrene-based preformed beads via atom transfer radical polymerization (ATRP) employing the CuBr/PMDETA catalyst system. Hydrophilic monomers including N,N-dimethylacrylamide (DMA) and poly(ethylene glycol) (PEG) macromonomers were grafted onto Merrifield type resin. Based on optical microscopic data, the particle sizes of the resins were increased in the order of 10 μm after the polymerization. This increment indicated that monomers are grafted not only to the particle surface but also to within a polymer matrix. These resins demonstrate well-swellability in polar solvent, and they enable high functional loadings up to 0.7-1.8 mmol g−1. The high loading capacity in polar solvents and favorable mechanical properties of resins render them to have great potential applications in peptide and oligonucletide syntheses.