Biodegradable polymers with advantageous physical and chemical properties are described, as well as methods for making such polymers. In one embodiment, a new chemical synthesis route to technologically important biodegradable poly(3-hydroxybutyrate) (P3HB) with high isotacticity and molecular weight required for a practical use is described. The new route can utilize racemic eight-membered cyclic diolide (rac-DL), meso-DL, or a rac-DL and meso-DL mixture, derived from bio-sourced dimethyl succinate, and enantiomeric (R,R)-DL and (S,S)-DL, optically resolved by metal-based catalysts. With a stereoselective racemic molecular catalyst, the ROP of rac-DL under ambient conditions produces rapidly P3HB with essentially perfect isotacticity ([mm]>99%), high crystallinity and melting temperature (T.sub.m=171 C.), as well as high molecular weight and low dispersity (M.sub.n=1.5410.sup.5 g/mol, =1.01).

Biodegradable polymers with advantageous physical and chemical properties are described, as well as methods for making such polymers. In one embodiment, a new chemical synthesis route to technologically important biodegradable poly(3-hydroxybutyrate) (P3HB) with high isotacticity and molecular weight required for a practical use is described. The new route can utilize racemic eight-membered cyclic diolide (rac-DL), meso-DL, or a rac-DL and meso-DL mixture, derived from bio-sourced dimethyl succinate, and enantiomeric (R,R)-DL and (S,S)-DL, optically resolved by metal-based catalysts. With a stereoselective racemic molecular catalyst, the ROP of rac-DL under ambient conditions produces rapidly P3HB with essentially perfect isotacticity ([mm] >99%), high crystallinity and melting temperature (T.sub.m=171 C.), as well as high molecular weight and low dispersity (M.sub.n=1.5410.sup.5 g/mol, =1.01).

This invention relates to the synthesis of multi-block bioresorbable polymers bearing hard and soft polymeric segments. The invention further relates to bioresorbable polymers for shape memory properties. The invention also relates to the use of such polymers as bone filler, vascular closure devices, hemostasis device, aneurysms, mastectomy devices and stent applications. The invention relates also to the use of such polymers for applications in fast degradation applications and 3D printing. The invention also relates to the use of such polymers as drug delivery platforms applications.

Techniques regarding the synthesis of one or more polymers through one or more ring-opening polymerizations conducted within a flow reactor and facilitated by one or more anionic catalysts are provided. For example, one or more embodiments can comprise a method, which can comprise polymerizing, via a ring-opening polymerization within a flow reactor, a cyclic monomer in the presence of one or more anionic organocatalysts.

Novel processes of preparing block polyester copolymers while precisely controlling the stereoconfiguration (e.g., tacticity), chemical composition and/or length of each unit (block) are provided. Block polyester copolymers featuring desirable combinations of two or more blocks featuring different stereoconfiguration (e.g., tacticity), chemical composition and/or length, including triblock, tetrablock and higher block copolymers are also provided. A novel family of organometallic magnesium complexes and uses thereof in preparing polyesters and block polyester copolymers are also provided.

A method for preparing a film of solid polymer electrolyte, including: (i) providing a composition including, in one or more solvents, at least one (co)polymer of at least one cyclic monomer selected from lactones and cyclic carbonates with five to eight ring members; the (co)polymer or (co)polymers having free terminal hydroxyl functions; at least one crosslinking agent, at least one ionic conductive salt; and optionally, in the case of a crosslinking agent bearing at least one photosensitive reactive function, at least one photoinitiator compound; (ii) forming a dry film from the composition, in conditions unfavourable to crosslinking of the (co)polymer or (co)polymers; and (iii) bringing the film into conditions favourable to crosslinking of the (co)polymer or (co)polymers to form the film of solid polymer electrolyte. Also disclosed is a film of solid polymer electrolyte and use thereof in an electrochemical system, in particular in a lithium battery.

In one or more embodiments, the present invention is directed to a novel method for synthesizing Mg(BHT).sub.2(THF).sub.2 catalyst, which has several advantages over previous methods. Dry toluene or pentane are not required for synthesizing the catalyst, and the reaction is done in a bulk solution of BHT and THF. Further, because the Mg(BHT).sub.2(THF).sub.2 is made in a one-step (one-pot) synthesis, the time required for synthesizing and drying the catalyst is reduced. Using the new method of the present invention, the Mg(BHT).sub.2(THF).sub.2 is pure after removing excess THF, thereby eliminating the need for washes and recrystallization.

A method for synthesizing a polybutylene adipate terephthalate-polylactic acid (PBAT-PLA) copolyester, the method including: uniformly blending a first prepolymer PBAT and a second prepolymer PLA to yield a mixture, 0putting the mixture in a vacuum reactor with a vacuum degree of between 5 and 100 pascal, heating the vacuum reactor to a temperature of between 100 and 110 C., and allowing to react for between 0.5 and 1 hr; stepwise increasing the temperature to be between 145 and 155 C. in between 1 and 2 hrs, and allowing to react for between 5 and 10 hrs, to yield a PBAT-PLA copolyester with a weight-average molecular weight of between 100000 and 250000. The method for synthesizing the PBAT-PLA copolyester is eco-friendly, non-toxic and cost-efficient.

It is provided a method for manufacturing a hyperbranched polyester polyol derivative, comprising the following steps: a) reacting only glycidol and -caprolactone at a temperature lying in a range of between 40 C. and 140 C. to obtain a hyperbranched polyester polyol in which caprolactone residues are randomly arranged; b) reacting the hyperbranched polyester polyol of step a) with a sulfation reagent to obtain a sulfated hyperbranched polyester polyol as hyperbranched polyester polyol derivative.

It is provided a method for manufacturing a hyperbranched polyester polyol derivative, comprising the following steps: a) reacting only glycidol and -caprolactone at a temperature lying in a range of between 40 C. and 140 C. to obtain a hyperbranched polyester polyol in which caprolactone residues are randomly arranged; b) reacting the hyperbranched polyester polyol of step a) with a sulfation reagent to obtain a sulfated hyperbranched polyester polyol as hyperbranched polyester polyol derivative.