Abstract
AbstractBy the use of various boron compounds methyl methacrylate and styrene were copolymerized under photoirradiations at −20°C. The alternately regulating activities of the boron compounds in the copolymerizations were in the following order: boron trichloride > ethylboron dichloride > boron trifluoride > diethylboron chloride ≫ triethylboron (≃0). Boron trichloride and ethylboron dichloride exhibited such high regulating activities that their presence in 1 mol% in the charged methyl methacrylate was sufficient to complete equimolar alternating copolymerization. The alternating copolymerization proceeded in the steady state. The copolymerization rates decreased in the following order: boron trichloride ≫ ethylboron dichloride > diethylboron chloride ≫ triethylboron (≃0). The cotacticities of methyl methacrylate‐centered triads in the resulting copolymers were identical to those prepared with boron trichloride, ethylboron dichloride, and diethylboron chloride. The mechanism of the alternating copolymerization is discussed.
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