Abstract
In the catalytic chain transfer polymerization of methyl methacrylate, butyl methacrylate and 2‐ethylhexyl methacrylate in toluene, it was found that the chain transfer constants (C~T~) were independent of solvent concentration and therefore of solution viscosity, and did not differ from the bulk polymerization values. For a diffusion controlled system, theoretical calculations predict an increase in C~T~ when the solution viscosity is lowered. This points at a non‐diffusion controlled catalytic chain transfer step. These results were obtained when the solvent was thoroughly purified using a Grubbs‐type set‐up, whereas a large reduction in C~T~ was found in unpurified solvent. Similar results were obtained for butyl acetate. Therefore it is concluded that the decrease of C~T~ in non‐purified solvents is not related to the solvent itself, but to solvent impurities. Further we found that methyl methacrylate ended radicals do not covalently bind to the cobalt complex, in contrast to styrene and acrylate ended radicals.
Chain transfer constant for the CCT polymerization of 2‐ethylhexyl methacrylate in toluene, and predictions for diffusion controlled systems.
magnified imageChain transfer constant for the CCT polymerization of 2‐ethylhexyl methacrylate in toluene, and predictions for diffusion controlled systems.