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Characterization of Aliphatic Polyesters Synthesized via Enzymatic Ring-Opening Polymerization in Ionic Liquids

机译:通过离子液体中酶的开环聚合反应合成的脂肪族聚酯的表征

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To evaluate the effects of ionic liquids (ILs) on the microstructural features of aliphatic polyesters for biomedical applications, a series of copolymers were synthesized by lipase ring opening polymerization of rac -lactide ( rac -LA) and ε-caprolactone (CL). The chemical structures of resulting polymers were characterized by 1 H- and 13 C-NMR and the average molecular weight ( M n ) and dispersity index were characterized by gel permeation chromatography. The structure of the copolymers confirms the presence of linear polymer chains with end-functional hydroxyl groups allowing covalent coupling of the therapeutic agents. Chain microstructure of copolymers indicates the presence of both random and block copolymers depending on the synthesis conditions. Moreover, it was found that CL is the most active co-monomer during copolymerization which enhances the polymerizability of rac -LA and allows to obtain higher M n of the copolymers. The results demonstrate that ILs could be promising solvents in synthesis of aliphatic esters for biomedical applications.
机译:为了评估离子液体(ILs)对用于生物医学应用的脂肪族聚酯的微观结构特征的影响,通过外消旋丙交酯(rac -LA)和ε-己内酯(CL)的脂酶开环聚合反应,合成了一系列共聚物。所得聚合物的化学结构通过1 H-和13 C-NMR表征,并且平均分子量(M n)和分散指数通过凝胶渗透色谱表征。共聚物的结构证实了具有末端官能羟基的线性聚合物链的存在,从而允许治疗剂共价偶联。共聚物的链微结构表明无规共聚物和嵌段共聚物的存在,这取决于合成条件。此外,发现CL是共聚期间最活跃的共聚单体,其增强了rac-LA的可聚合性并允许获得更高的共聚物的M n。结果表明,ILs可能是用于生物医学应用的脂族酯合成的有前途的溶剂。

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