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    壳聚糖-O-聚(寡聚乙二醇甲基丙烯酸酯)的原子转移自由基聚合与表征

    Chitosan-O-Poly(oligo(ethylene glycol) methacrylate)Brush Polymers:ATRP Synthesis and Characterization

    • 摘要: 基于原子转移自由基聚合(ATRP)和十二烷基硫酸钠(SDS)壳聚糖(CS)复合物(SCC)的位置选择性改性策略,合成了结构可控的壳聚糖-O-聚(寡聚乙二醇甲基丙烯酸甲酯)(CSPOEGMA)刷状衍生物。通过在SCC的羟基上引入溴代异丁酸后脱除SDS得到大分子引发剂O溴化壳聚糖(CS-Br)。用红外光谱(FT-IR)与核磁共振(1HNMR)表征了产物结构。结果表明:改变溴代度(DS)可调节聚(寡聚乙二醇甲基丙烯酸甲酯)(POEGMA)的接枝度,而改变寡聚乙二醇甲基丙烯酸甲酯(OEGMA)与CSBr

       

      Abstract: Chitosanderived brush polymers with welldefined chemical structure were synthesized by combining ATRP with sodium dodecyl sulphatechitosan complex (SCC)based regioselective modification strategy. ATRP macromolecular initiator, O-bromobutyrated CS (CS-Br), was conveniently prepared by grafting bromoisobutyrate onto the hydroxy groups of SCC and subsequently removing SDS from the Obromobutyrated SCC. The structure of product was characterized by FTIR and 1HNMR. Results showed that the grafting level of POEGMA could be adjusted by varying the degree of substitution (DS) of bromobutyrate. By changing molar feeding ratio of OEGMA to CSBr, the degree of polymerization of POEGMA could be modulated.

       

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