“…At the same time, the differences should be noted between the conditions of ring-opening polymerisation between small lactones and macrolactones that are caused by little or no ring strain in the case of the compounds with 12 or more atoms, which requires specific catalysts to obtain optimal yields [ 2 , 3 , 4 , 5 , 6 , 7 , 8 ]. Recently, one of the most studied macrolactones that is of particular interest is ethylene brassylate (EB), a 17-membered lactone ring, investigated essentially by ring-opening polymerisation [ 9 , 10 , 11 , 12 , 13 , 14 , 15 , 16 , 17 , 18 , 19 ]. The synthesised homopolymer, as well as other different EB-based block/copolymers, can provide an amphiphilic character; for example, in the poly(ethylene glycol)-b-poly(ethylene brassylate) copolymer [ 10 ], a higher crystallisation rate of about 67 °C and chains easily susceptible to hydrolytic degradation in the case of copolymers based on D, L-lactide and EB [ 13 ] improved mechanical behaviour, flexibility, and ductility compared to polylactides, since only a molar content of 5% EB comonomer increases the elongation at break from 2 to 87% [ 13 ], and also due to a self-assembled morphology, building block capacity, and network formation.…”