Quinone transfer radical polymerization (QTRP) of styrene: Catalysis by different metal complexes

Styrene has been polymerized by a Quinone Transfer Radical Polymerization (QTRP) based on the redox reaction of an ortho‐quinone and a metal catalyst. Several metal acetylacetonates have been tested in this work. The radical polymerization of styrene is largely controlled when phenanthrenequinone (PhQ) is used with catalytic amounts of Co(acac)₂, Ni(acac)₂, Mn(acac)_{2 or 3}, and Al(acac)₃. As a rule, in the presence of all these metallic complexes, the polystyrene molar mass increases with the monomer conversion, and polydispersity (M_w/M_n) is in the 1.3–1.6 range (at least until 40% monomer conversion). Styrene polymerization has also been resumed by polystyrene chains prepared by QTRP. In the specific case of manganese acetylacetonates, an amine or phosphine ligand has to be added for the control to be effective. Finally, two mechanistic hypotheses have been proposed, depending on whether the oxidation state of the metal can be easily changed or not. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 2723‐2733, 2005