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Stereocontrol during the free‐radical polymerization of methacrylamides in the presence of Lewis acids
Authors:Yutaka Isobe  Yoshikatsu Suito  Shigeki Habaue  Yoshio Okamoto
Abstract:The effects of Lewis acids, that is, rare earth metal trifluoromethanesulfonates, on the free‐radical polymerization of N‐methylmethacrylamide (MMAM), N‐isopropylmethacrylamide (IPMAM), Ntert‐butylmethacrylamide (tBMAM), N‐phenylmethacrylamide (PMAM), and methacrylamide were examined under various conditions. A catalytic amount of Yb(OSO2CF3)3 significantly affected the stereochemistry during the radical polymerization. Polymerization solvents strongly influenced the effect of the Lewis acids. Methanol was the best solvent for increasing the isotactic specificity during the polymerization of MMAM and IPMAM, whereas tetrahydrofuran was more effective for the tBMAM and PMAM polymerizations. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 1027–1033, 2003
Keywords:radical polymerization  methacrylamides  stereospecific polymers  isotactic  Lewis acid
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