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A novel route to poly(2-hydroxyethyl methacrylate) and its amphiphilic block copolymers
Authors:Eli Ruckenstein  Hongmin Zhang
Abstract:The vinyl of the ester group of 2-vinyloxyethyl methacrylate was first selectively reacted with acetic acid to obtain 2-1-(acetoxy)ethoxy]ethyl methacrylate ( 2 ). This protected monomer was subjected to anionic polymerization in tetrahydrofuran at ?60°C in the presence of LiCl, using 1,1-diphenylhexyllithium as initiator. The molecular weight of the polymer could thus be controlled and a narrow molecular weight distribution obtained. The protecting group, 1-(acetoxy)ethyl, could be easily eliminated (by quenching the polymerization reaction with methanol and water) to generate poly(2-hydroxyethyl methacrylate) (poly(HEMA)). Block copolymers were also prepared by the sequential anionic polymerization of MMA and 2 or styrene and 2 . They possess narrow molecular weight distributions, and controlled molecular weights and compositions. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 1865–1872, 1998
Keywords:anionic polymerization  poly(2-hydroxyethyl methacrylate)  amphiphilic block copolymer  poly(methyl methacrylate)-b-poly(2-hydroxyethyl methacrylate)  poly(styrene)-b-poly(2-hydroxyethyl methacrylate)
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