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Pure aluminum isopropoxide was shown to be a highly active catalyst for the polymerization of ε-caprolactone: the overall kinetics of this polymerization follow a first current order in monomer and a first order in catalyst. Mechanistical studies indicate also that this system operates through a selective acyloxygen cleavage of the lactone ring, with insertion in the aluminum-oxygen bond. Moreover, the polymerization proceeds by a perfectly “living” process on catalytic coordination aggregates.
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Ouhadi et al. (1975) studied this question.
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