Polylactones, 7. The mechanism of cationic polymerization of β-propiolactone and ϵ-caprolactone

Homopolymerisations of β-propiolactone and ?-caprolactone, initiated by means of methyl trifluorosulfonate, triethyloxonium tetrafluoroborate or acetylium perchlorate, were investigated. Both ¹H and ¹³C NMR spectra proved that the alkylating initiators yield polyesters with alkyl ester end groups, indicating a chain growth via alkyl-oxygen cleavage of the lactone. At temperatures below 100°C cationic polymerizations initiated by alkylating reagents were found to proceed via end groups which may cause degradation due to back-biting. When ?-caprolactone was reacted with excess methyl triflate, high concentration of triflate ester end groups were formed, whereas in the case of β-propiolactone active end groups were not detectable by ¹H NMR spectroscopy. Initiation with acetylium perchlorate yielded a polyester with acetate end groups. Acetate end groups were also obtained, when “living” polymers, initiated with methyl triflate, were reacted with acetic anhydride. It could be shown that the formation of acetate end groups does not indicate an electrophilic attack at the endocyclic oxygen. Furthermore, it is discussed that any experimental evidence for a cationic chain growth via acyloxygen bond cleavage is lacking.