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Oligo(glycerol) Methacrylate Macromonomers
Authors:Anja Thomas  Florian K Wolf  Holger Frey
Abstract:Linear, protected ω‐methoxy oligo(glycerol) methacrylate (OGlyPMA) macromonomers are synthesized via anionic ring‐opening polymerization of ethoxyethyl glycidyl ether (EEGE) followed by termination with methacrylic acid anhydride (equation image = 3–11, PDI < 1.30). The covalently bound methacrylate moiety allows the homopolymerization of OGlyPMA as well as copolymerization with low molecular weight comonomers. In homopolymerizations, macromonomers are polymerized by atom transfer radical polymerization (ATRP) yielding well‐defined graft polymers (equation image = 20 000–30 000 g mol−1). Acidic hydrolysis of the protecting groups releases water‐soluble polyhydroxy‐functional structures. First results on the copolymerization with 2‐hydroxyethyl methacrylate (HEMA) are given in the final part of this work.
Keywords:macromonomers  polyethers  polyglycerol  poly(hydroxyethyl methacrylate)  water‐soluble polymers
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