Abstract
Vinyl acetate polymerization initiated by azo radical sources in the presence of cobalt(II) tetramesitylporphyrin ((TMP)Co II ) shows an induction period followed by an organo-cobalt mediated living radical polymerization (LRP). The induction period corresponds to converting (TMP)Co II to an organo-cobalt porphyrin derivative (organo-Co(TMP)). Living character at low vinyl acetate conversion is demonstrated by a linear increase in molecular weight with conversion, relatively low polydispersity homopolymers, and formation of block copolymers with methyl acrylate ((TMP)Co-PVAc-b-PMA). Deviations from ideal LRP occur by radical termination and chain transfer events at moderate conversion of vinyl acetate (VAc). Mechanistic studies demonstrate that the VAc radical polymerization is controlled by a degenerative transfer mechanism that utilizes organo-cobalt complexes as the transfer agent. Kinetic studies are utilized in comparing radical polymerization of vinyl acetate and methyl acrylate that are mediated by organo-cobalt complexes. © 2008 American Chemical Society.