Enzyme-catalyzed polycarbonate and polycarbonate ester synthesis
View Patent ↗An enzymatic process for preparing aliphatic polycarbonates via terpolymerization or transesterification using a dialkyl carbonate, an aliphatic diester, and an aliphatic diol or triol reactant. A catalyst having an enzyme capable of catalyzing an ester hydrolysis reaction in an aqueous environment is subsequently added to the reaction mixture. Next, polymerization of the reaction proceeds for an allotted time at a temperature≦100° C. Finally, the copolymer is isolated from an the catalyst via filtration.
1. A method for preparing a poly(carbonate-co-ester) polymer by enzyme catalysis comprising:
(a) selecting reactants for a reaction such that a first reactant is a dialkyl carbonate, a second reactant is an aliphatic diester, a third reactant is an aliphatic diol or triol reactant, and a fourth reactant is a cyclic lactone, and combining the reactants as a reaction mixture;
(b) selecting a catalyst capable of catalyzing an ester hydrolysis reaction in an aqueous environment;
(c) adding the catalyst to the reaction mixture and allowing polymerization to proceed; and
(d) isolating the product poly(carbonate-co-ester).
2. The method according to claim 1 , wherein carbonate units along chains are formed by reactions between diols/triols and alkyl carbonates and ester repeat units are formed by lactone ring-opening.
3. The method according to claim 2 , wherein the dialkyl carbonate has the formula CO(OR) 2 wherein R represents a straight-chain or branched C1-C5-alkyl (CnH 2n+1 ).
4. The method according to claim 2 , wherein the aliphatic ester has the formula R—((CO)—R1) 2 wherein R represents a generalized group.
5. The method according to claim 2 , wherein the aliphatic diol or triol has the formula HO—R—OH wherein R represents a generalized group.
6. The method according to claim 2 , wherein the lactones are selected from the group consisting of ε-caprolactone, para-dioxanone, glycolide, macrolactones, ω-pentadecalactone, and other lactones capable of preparing polyesters by enzyme-catalyzed lactone ring-opening polymerizations.
7. The method according to claim 3 , wherein the dialkyl carbonate is selected from the group consisting of: dimethyl, diethyl, di(n-propyl), di(n-butyl), di(sec-butyl), diisobutyl, di(tert-butyl), di(n-pentyl), diisoamyl, and dineopentyl carbonates.
8. The method according to claim 4 , wherein the aliphatic ester is selected from the group consisting of: linear or branched hydrocarbon groups having 3-10 carbon atoms; linear or branched C4-C8 diacids; and a mixture of diacids.
9. The method according to claim 5 , wherein the aliphatic diol is selected from the group consisting of: 1,2-ethanediol, 1,3-propanediol, 1,4-butanediol, 1,6-hexanediol, 1,5-pentanediol, 1,10-decanediol, 2-methyl-1,3-propanediol, 2-methyl-2-butyl-1,3-propanediol and 2,2-dimethyl-1,4-butanediol, neopentylglycol hydroxypivalate, diethylene glycol, triethylene glycol, and methyldiethanolamine.
10. The method according to claim 5 , wherein the triol has 2 primary hydroxyl groups forming a linear polycarbonate polyol.
11. The method according to claim 5 , wherein the triol has 3 primary hydroxyl groups forming a hyper-branched polymer.
12. The method according to claim 5 , wherein the triol is glycerol or tris-hydroxymethyl ethane.
13. The method according to claim 2 , wherein the reaction temperature of the method is ≦100° C.
14. The method according to claim 2 , wherein the first stage is pressurized under low vacuum and the second stage is pressured under high vacuum.
15. The method according to claim 2 , wherein the copolymer is poly(BC-co-BS), has a polydisperity between 1.7 and 2.0, upon completion has a molecular weight≧9 800, and has a random or block distribution of BC and BS units.
16. The method according to claim 15 , wherein the highest molecular weight of the copolymer upon completion of the reaction is derived at a reaction temperature of approximately 80° C.
17. The method according to claim 2 , wherein the copolymer is poly(HC-co-HA), has a polydisperity between 1.5 and 1.6, upon completion has a molecular weight≧14 800, and has a random or block distribution of HC and HA units.
18. The method according to claim 17 , wherein a molecular weight of the copolymer gradually increases as temperature increases.
19. The method according to claim 1 , wherein the enzyme is selected from the group consisting of lipases and cutinases.
20. The method according to claim 15 , wherein end-group structures of poly(BC-co-BS) are defined by:
(a) fixing the molar ratio of DES to BD at 0.5:1; and
(b) varying the molar ratio of DEC to (BD-DES) while (BD-DES) remains constant,
wherein the content of hydroxyl end groups in polymer chains are decreased and the content of ethyl carbonate plus ethyl ester end groups in copolymers are increased.