The homopolymerization of methyl methacrylate (MMA) in the presence of 2,2,6,6-tetramethyl-l-piperidinyloxy (TEMPO) is described and compared to the TEMPO-mediated polymerization of styrene. Furthermore, the formation of block copolymers between MMA and styrene from polystyrene chains with TEMPO fra
Synthesis of block copolymers via redox polymerization
✍ Scribed by Oya Gali̇oğlu Atici; Ahmet Akar; Yusuf Ayar; Oğuz Meci̇t
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- English
- Weight
- 237 KB
- Volume
- 71
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
✦ Synopsis
Polymerization and copolymerization of vinyl monomers such as acrylamide, acrylonitrile, vinyl acetate, and acrylic acid with a redox system of Ce(IV) and organic reducing agents containing hydroxy groups were studied. The reducing compounds were poly(ethylene glycol)s, halogen-containing polyols, and depolymerization products of poly(ethylene terephthalate). Copolymers of poly(ethylene glycol)s-b-polyacrylonitrile, poly(ethylene glycol)s-b-poly(acrylonitrile-co-vinyl acetate), poly(ethylene glycol)s-b-polyacrylamide, poly(ethylene glycol)s-b-poly(acrylamide-co-vinyl acetate), poly(1-chloromethyl ethylene glycol)-bpoly(acrylonitrile-co-vinyl acetate), and bis[poly-(ethylene glycol terephthalate)]-b-poly(acrylonitrile-co-vinyl acetate) were produced. The yield of acrylamide polymerization and the molecular weight of the copolymer increased considerably if about 4% vinyl acetate was added into the acrylamide monomer. However, the molecular weight of the copolymer was decreased when 4% vinyl acetate was added into the acrylonitrile monomer. Physical properties such as solubility, water absorption, resistance to UV light, and viscosities of the copolymers were studied and their possible uses are discussed.
📜 SIMILAR VOLUMES
End-functional polystyrenes with an N,N-diethyldithiocarbamyl group were prepared by the photopolymerization of styrene with novel diethyldithiocarbamate derivatives as photoiniferters. Under ultraviolet light, the end-functional polymers could initiate a second monomer to polymerize and form block
A series of triblock copolymers of the type A-B-A were synthesized using tungsten chloride-anchored hydroxyl-terminated polybutadiene (HTPBD) catalyst. Monomers like phenylacetylene (PA), norbornene (NBE), cyclooctadiene (COD), and cyclopentene (CP) were polymerized via metathesis pathway using this