Abstract
The radical polymerization of methyl methacrylate catalyzed by systems based on the carborane complexes of ruthenium(III) is studied in the presence of a number of activating agents: tin 2-ethyl hexanoate, aluminum isopropoxide, isopropylamine, and AIBN. It is shown that in the presence of the systems under consideration, polymerization proceeds in a controlled mode via the ATRP mechanism (AGET or ICAR ATRP) at catalyst concentrations with ppm level relative to that of the monomer. As the degree of monomer conversion grows, the molecular weight of the polymer increases linearly while its polydispersity coefficients decrease linearly. The role of the mentioned agents is to transfer the catalyst to the active form containing a metal atom in the oxidation number +2 and able to interact with halogen-terminated dormant polymer chains. It is first shown that the carborane complexes of ruthenium(II) are applicable for the catalysis of controlled radical polymerization.
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