Free-radical copolymerization of ethyl α-hydroxymethylacrylate with methyl methacrylate by reversible addition–fragmentation chain transfer

Autor: Rocío Cuervo-Rodríguez, Manuel Sánchez-Chaves, Marta Fernández-García, Vanesa Bordegé
Rok vydání: 2006
Předmět:
Zdroj: Journal of Polymer Science Part A: Polymer Chemistry. 44:5618-5629
ISSN: 1099-0518
0887-624X
DOI: 10.1002/pola.21702
Popis: The controlled free-radical homopolymerization of ethyl α-hydroxymethylacrylate and copolymerization with methyl methacrylate were performed in chlorobenzene at 70 °C by the reversible addition–fragmentation chain transfer polymerization technique with 2,2′-azobisisobutyronitrile as the initiator. 2-Phenylprop-2-yl dithiobenzoate and 2-cyanoprop-2-yl dithiobenzoate were used as chain-transfer agents in the homopolymerization, whereas only the former was used in the copolymerization. All reactions presented pseudolinear kinetics. The effect of the monomer feed ratio on the copolymerization kinetics was examined. The conversion level decreased when the proportion of ethyl α-hydroxymethylacrylate in the monomer feed was larger. Kinetic studies indicated that the radical polymerizations proceeded with apparent living character according to experiments, demonstrating an increase in the molar mass with the monomer conversion and a relatively narrow molar mass distribution. All copolymers were statistical in chain structure, as confirmed by determinations of the monomer reactivity ratios. The monomer reactivity ratios were determined, and the Mayo–Lewis terminal model provided excellent predictions for the variations of the intermolecular structure over the entire conversion range. Additionally, the chemical modification of poly(ethyl α-hydroxymethylacrylate) was carried out to introduce glucose pendant groups into the structure. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 5618–5629, 2006
Databáze: OpenAIRE
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