Triblock copolyesters derived from lactic acid and glucose: synthesis, nanoparticle formation and simulation

ABA triblock copolyesters were synthesized by ring-opening polymerization (ROP) of l-lactide in solution initiated by a telechelic d-glucose-based polyester macroinitiator. The macroinitiator with a number-average molecular weight about 2500 g mol-1 was synthesized by non-stoichiometric polycondensation in the melt of 2,4:3,5-di-O-methylene-d-glucitol and dimethyl succinate. Two triblock copolyesters of Mn ranging between ~6000 and ~9000 g mol-1, and differing in the length of the polylactide blocks were prepared. These copolyesters started to decompose when heated at ~220 °C and degraded slowly upon aqueous incubation under physiological conditions. They did not display any perceivable crystallinity and showed a single glass transition temperature (Tg) around 60 °C with the higher value corresponding to the larger content in glucitol units. The copolyesters were able to form nanoparticles with average diameters of ~100–130 nm and satisfactory dispersity. The effect of the block lengths on size, ¿-potential values and physical stability of the nanoparticles was evaluated. A molecular dynamics simulation study allowed modelling the two-phase structure of the nanoparticles and evidenced the preference of the glucose-based block to be peripherally located.Peer ReviewedPostprint (author's final draft

Enzymatic recycling of polymacrolactones

The use of renewable monomers to make new polyesters which could replace the ones obtained from petrochemical resources employing green processes is attracting a lot of attention these days. With this in mind, three different macrolactones, ¿-pentadecalactone, globalide and 6-hexadecenlactone, have been polymerized in bulk by enzymatic ring opening polymerization (e-ROP) using immobilized Candida antarctica lipase B to give their corresponding polymacrolactones (PMLs). For the first time, these PMLs have been depolymerized enzymatically in solution with the concourse of the same enzyme and at mild temperatures. GPC, NMR and ESI MS demonstrated that the main products recovered after the enzymatic processive recycling were cyclic monomers and dimers, with a small amount of higher size macrocyclic oligoesters (MCOs). It was observed that these depolymerizations followed a Michaelis–Menten kinetic model. Finally it was shown that these MCOs could be repolymerized. This research provides a biosynthetic method for chemical recycling of these interesting polymeric materials providing a pathway towards a circular economy.Peer ReviewedPostprint (author's final draft

Triblock copolyesters derived from lactic acid and glucose: synthesis, nanoparticle formation and simulation

ABA triblock copolyesters were synthesized by ring-opening polymerization (ROP) of l-lactide in solution initiated by a telechelic d-glucose-based polyester macroinitiator. The macroinitiator with a number-average molecular weight about 2500 g mol-1 was synthesized by non-stoichiometric polycondensation in the melt of 2,4:3,5-di-O-methylene-d-glucitol and dimethyl succinate. Two triblock copolyesters of Mn ranging between ~6000 and ~9000 g mol-1, and differing in the length of the polylactide blocks were prepared. These copolyesters started to decompose when heated at ~220 °C and degraded slowly upon aqueous incubation under physiological conditions. They did not display any perceivable crystallinity and showed a single glass transition temperature (Tg) around 60 °C with the higher value corresponding to the larger content in glucitol units. The copolyesters were able to form nanoparticles with average diameters of ~100–130 nm and satisfactory dispersity. The effect of the block lengths on size, ¿-potential values and physical stability of the nanoparticles was evaluated. A molecular dynamics simulation study allowed modelling the two-phase structure of the nanoparticles and evidenced the preference of the glucose-based block to be peripherally located.Peer Reviewe