A successive method for preparing novel amphiphilic graft copolymers with a hydrophilic backbone and hydrophobic side chains was developed. An anionic copolymerization of two bifunctional monomers, namely, allyl methacrylate (AMA) and a small amount of glycidyl methacrylate (GMA), was carried out in
A novel route to poly(2-hydroxyethyl methacrylate) and its amphiphilic block copolymers
β Scribed by Eli Ruckenstein; Hongmin Zhang
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 166 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0887-624X
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β¦ Synopsis
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 060ΠC 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.
π SIMILAR VOLUMES
2-Hydroxyethyl methacrylate (0Γ01 mol) was allowed to react with 0Γ01 mol of hexamethylene di-isocyanate and the product was coupled to 0Γ01 mol of b-cyclodextrin to form a new cyclodextrin-based copolymer. The interaction of the polymer with di β erent steroids was investigated and the extent of ads
## Abstract Diblock copolymers of poly(Lβlactide)β__block__βpoly(methyl methacrylate) (PLLAβ__b__βPMMA) were synthesized through a sequential twoβstep strategy, which combines ringβopening polymerization (ROP) and atom transfer radical polymerization (ATRP), using a bifunctional initiator, 2,2,2βtr