NMR studies on the stereospecific polymerization of methyl vinyl ether. Part II. Polymerization by sulfuric acid–aluminum sulfate complex: Enantiomorphic catalyst sites model

Abstract

AbstractHighly crystalline poly(methyl vinyl ether) (PMVE) was produced in toluene in a temperature range of 0 to −20°C. with the use of sulfuric acid–aluminum sulfate complex (SA catalyst). It was found from the NMR spectra that these polymers contained more than 50% of the triad isotactic fraction and the melting point of the unfractionated polymer was about 130°C. However, PMVE containing a large amount of the isotactic fraction was insoluble in nitromethane, so the triad tacticity of highly crystalline PMVE could not be quantitatively determined. The molecular weight of PMVE increased with increasing conversion and increasing polymerization temperature. This behavior is different from that in metal halide catalysts. Also, the stereoregularity of PMVE decreased with increasing monomer concentration. However, addition of a polar solvent and increasing the polymerization temperature had little effect on the stereoregularity of the polymer. The increase in the isotactic fraction at high catalyst concentration and the difference in the monomer composition in the copolymerization of methyl vinyl ether with 2‐chloroethyl vinyl ether by SA catalyst from that obtained by BF3·O(C2H5)2 suggest that the absorption of MVE on a catalyst surface is an important step in the propagation step by SA catalyst. The fraction of the triad tacticity calculated from the enantiomorphic catalyst sites model8 coincided with the experimental results. This fact shows that the steric structure of the adding monomer is determined only by the nature of the catalyst irrespective of the nature of a growing chain end. It is concluded, on considering also the results of the previous paper, that completely different factors can control the steric structure of a polymer even for the same monomer when different catalysts are used.