Abstract
The kinetics and mechanism of the polymerization of isobutylene catalyzed by FeCl3 center dot ether complexes in hexane at 0 degrees C were investigated. The polymerization rates increased in the diisopropyl ether< 2-chloroethyl ethyl ether < bis(2-chloroethyl) ether order, attributed to electronic effects. The polymerization rates increased with increasing initiator and catalyst concentrations. The first order plots, however, deviated from the linear suggesting that the cation concentration decreases with time. The previously proposed mechanism is inadequate to explain this finding. The decrease in the polymerization rate with time is explained by the low solubility of the H+ROR'FeCl4- complexes that precipitate during polymerization. Based on mechanistic studies the revised mechanism now also includes the equilibrium H+ROR'FeCl4- reversible arrow HCl + FeCl3 center dot ROR'.