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首页> 外文期刊>Macromolecular rapid communications: Publishing the newsletters of the European Polymer Federation >Preparation of Clickable Poly(3-hydroxyalkanoate) (PHA): Application to Poly(ethylene glycol) (PEG) Graft Copolymers Synthesis
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Preparation of Clickable Poly(3-hydroxyalkanoate) (PHA): Application to Poly(ethylene glycol) (PEG) Graft Copolymers Synthesis

机译:可点击的聚(3-羟基链烷酸酯)(PHA)的制备:在聚(乙二醇)(PEG)接枝共聚物合成中的应用

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摘要

A new synthesis of amphiphilic biodegradable copolymers consisting of hydrophobic poly(3-hydroxyalkanoate) (PHA) backbone and hydrophilic poly(ethylene glycol) (PEG) units as side chains is described. Poly[(3-hydroxyoctanoate)-co-(3-hydroxyundecenoate)] (PHOU) was first methanolyzed and its unsaturated side chains were quantitatively oxidized to carboxylic acid. Esterification with propargyl alcohol led to an alkyne-containing "clickable" PHA in 71% conversion. Its reactivity was successfully demonstrated by grafting azide-terminated PEG chains of 550 and 5 000 g . mol(-1), respectively. All products were fully characterized using GPC, H-1, and COSY NMR.
机译:描述了由疏水性聚(3-羟基链烷酸酯)(PHA)主链和亲水性聚(乙二醇)(PEG)单元作为侧链的两亲生物可降解共聚物的新合成方法。首先将聚[(3-羟基辛酸酯)-共-(3-羟基十一碳酸酯)](PHOU)甲醇化,并将其不饱和侧链定量氧化为羧酸。用炔丙醇酯化得到含炔的“可点击的” PHA,转化率为71%。通过接枝550和5000 g叠氮化物末端的PEG链成功证明了其反应活性。 mol(-1)。所有产品均使用GPC,H-1和COZY NMR进行了全面表征。

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