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Aspects of Living Radical Polymerization Mediated by Cobalt Porphyrin Complexes
Author(s) -
Peng ChiHow,
Li Shan,
Wayland Bradford B.
Publication year - 2009
Publication title -
journal of the chinese chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.329
H-Index - 45
eISSN - 2192-6549
pISSN - 0009-4536
DOI - 10.1002/jccs.200900032
Subject(s) - chemistry , polymer chemistry , porphyrin , polymerization , methyl acrylate , cobalt , copolymer , catalytic chain transfer , living free radical polymerization , living polymerization , vinyl acetate , radical polymerization , dispersity , reversible addition−fragmentation chain transfer polymerization , cobalt mediated radical polymerization , chain transfer , acrylate , polymer , photochemistry , organic chemistry
Living radical polymerization (LRP) of methyl acrylate (MA), acrylic acid (AA), and vinyl acetate (VAc) mediated by cobalt(II) porphyrin complexes ((TMP)Co II ·, (TMPS)Co II ·) are reported. The polymeric products with relatively low polydispersity and controlled number average molecular weight ( M n ) based on one polymer chain per cobalt complex demonstrate the living characters of the polymerization process. The formation of block copolymers of poly(methyl acrylate)‐b‐poly(vinyl acetate) (PMA‐b‐PVAc) and poly(methyl acrylate)‐b‐poly(vinyl pyrrolidone) (PMA‐b‐PVP) demonstrate another important feature of LRP and extend the application of cobalt porphyrin mediated radical polymerization to a wider array of functionalized monomers. Kinetic studies using 1 H NMR to follow the formation of orGano‐cobalt complexes reveal that two mechanisms, reversible termination (RT) and degenerative transfer (DT), occur during the polymerization process. MA and VAc polymerization mediated by cobalt porphyrin complexes are used to illustrate the properties of these two LRP pathways and evaluate the kinetic and thermodynamic properties for several of the central reactions.