Bazin Alfred, Avérous Luc, Pollet Eric
BioTeam/ICPEES-ECPM, UMR CNRS 7515, Université de Strasbourg, 25 Rue Becquerel, CEDEX 2, 67087 Strasbourg, France.
Polymers (Basel). 2021 Oct 27;13(21):3693. doi: 10.3390/polym13213693.
Enzymatic synthesis of aromatic biobased polyesters is a recent and rapidly expanding research field. However, the direct lipase-catalyzed synthesis of polyesters from ferulic acid has not yet been reported. In this work, various ferulic-based monomers were considered for their capability to undergo CALB-catalyzed polymerization. After conversion into diesters of different lengths, the CALB-catalyzed polymerization of these monomers with 1,4-butanediol resulted in short oligomers with a DP up to 5. Hydrogenation of the double bond resulted in monomers allowing obtaining polyesters of higher molar masses with DP up to 58 and M up to 33,100 g·mol. These polyesters presented good thermal resistance up to 350 °C and T up to 7 °C. Reduction of the ferulic-based diesters into diols allowed preserving the double bond and synthesizing polyesters with a DP up to 19 and M up to 15,500 g·mol and higher T (up to 21 °C). Thus, this study has shown that the monomer hydrogenation strategy proved to be the most promising route to achieve ferulic-based polyester chains of high DP. This study also demonstrates for the first time that ferulic-based diols allow the synthesis of high T polyesters. Therefore, this is an important first step toward the synthesis of competitive biobased aromatic polyesters by enzymatic catalysis.
芳香族生物基聚酯的酶促合成是一个新兴且发展迅速的研究领域。然而,尚未有关于由阿魏酸直接通过脂肪酶催化合成聚酯的报道。在这项工作中,研究了各种基于阿魏酸的单体进行CALB催化聚合反应的能力。将这些单体转化为不同长度的二酯后,它们与1,4 - 丁二醇在CALB催化下聚合生成了聚合度高达5的短低聚物。双键氢化后得到的单体能够制备出聚合度高达58且摩尔质量高达33100 g·mol的更高摩尔质量的聚酯。这些聚酯在高达350 °C的温度下具有良好的耐热性,玻璃化转变温度高达7 °C。将基于阿魏酸的二酯还原为二醇能够保留双键,并合成聚合度高达19且摩尔质量高达15500 g·mol以及更高玻璃化转变温度(高达21 °C)的聚酯。因此,本研究表明单体氢化策略被证明是获得高聚合度的基于阿魏酸的聚酯链最有前景的途径。本研究还首次证明基于阿魏酸的二醇能够合成高玻璃化转变温度的聚酯。因此,这是通过酶催化合成具有竞争力的生物基芳香族聚酯的重要第一步。