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One-step chemoenzymatic synthesis of poly(epsilon-caprolactone-block-methyl methacrylate) in supercritical CO2

机译:超临界CO2中一步法化学酶法合成聚ε-己内酯嵌段甲基丙烯酸甲酯

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摘要

Enzymatic ring-opening polymerization (eROP) of epsilon-caprolactone (epsilon-CL) and atom-transfer radical polymerization (ATRP) of methyl methacrylate (MMA) were integrated into a one-step chemoenzymatic route to yield poly(epsilon-CL-block-MMA) (PCL-b-PMMA) in supercritical carbon dioxide (scCO2). The interaction between eROP and ATRP during the copolymerization was studied: Cu(I) Br/bpy as ATRP catalyst was compatible with eROP, while Ni(PPh)(3)Br-2 inhibited enzyme activity; under the reaction conditions, both epsilon-CL and PCL improved the solubility of poly(MMA) (PMMA) in the reaction system, and thus the ATRP proceeded successfully. The propagation of PMMA block exhibited living kinetics during the copolymerization, ensuring the molecular weight was well controlled. PCL-b-PMMA copolymers with varying molecular weight were synthesized with good control of the composition of the block copolymer. The one-step chemoenzymatic polymerization provides a very simple and versatile route for the synthesis of block copolymers.
机译:将ε-己内酯(ε-CL)的酶开环聚合(eROP)和甲基丙烯酸甲酯(MMA)的原子转移自由基聚合(ATRP)整合到一步化学酶法路线中,生成聚ε-CL-嵌段-MMA)(PCL-b-PMMA)中的超临界二氧化碳(scCO2)。研究了共聚过程中eROP与ATRP之间的相互作用:作为ATRP催化剂的Cu(I)Br / bpy与eROP相容,而Ni(PPh)(3)Br-2抑制了酶活性。在反应条件下,ε-CL和PCL均提高了聚(MMA)(PMMA)在反应体系中的溶解度,从而使ATRP顺利进行。 PMMA嵌段的扩散在共聚过程中表现出活性,确保分子量得到很好的控制。合成了分子量变化的PCL-b-PMMA共聚物,并很好地控制了嵌段共聚物的组成。一步化学酶促聚合为嵌段共聚物的合成提供了一种非常简单和通用的途径。

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