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机构地区:[1]武汉大学化学与分子科学学院
出 处:《武汉大学学报(理学版)》2007年第2期165-169,共5页Journal of Wuhan University:Natural Science Edition
基 金:国家自然科学基金资助项目(20572081)
摘 要:给出了新型功能化单体5-苄氧甲基-1,4-二氧六环-2-酮(BDON)的合成方法,并将其中间体5-羟甲基-1,4-二氧六环-2-酮(HDON)的产率由文献值的35%提高到48%,同时还研究了BDON在不同催化剂Sn(Oct)2、Al(OiPr)3和Al(OiBu)3的存在下的本体开环聚合,得到分子量为19 200的聚合物,研究了聚合温度、时间、催化剂以及催化剂浓度对单体转化率和分子量的影响.通过催化氢化去除苄基保护基得到聚(5-羟甲基-1,4-二氧六环-2-酮)(PHDON),并用FTIR、1H NMR、13C NMR和GPC等方法对聚合物进行了表征.另外,研究了3种聚合物PHDON、PBDON和PDON在不同条件下的体外降解速率以及BDON和DON的共聚和聚合物的亲水性.This paper described the synthesis of a new functional dioxanone monomer, 5-benzyloxym-ethyl-1,4-dioxan-2-one (BDON), and the yield of poly(5-hydroxy-methyl-1,4-dioxan-2-one) (HDON) was enhanced from 35G reported to 48G. We also studied on its ring-opening polymerization in bulk using Sn (Oct)2, AI(O^iPr)3 or Al(O^iBu)3 as an initiator. The polymer was obtained with a molecular weight of 19 200. The influence of reaction conditions, such as polymerization temperature, time, initiator and initiator concel^tration on the monomer conversion, and molecular weight have been investigated. The protecting benzyl group was removed subsequently by catalytic hydrogenation to give poly(5-hydroxymethyl-1,4- dioxan-2-one) (PHDON) with pendant hydroxyl groups. The polymers obtained were characterized by FTIR, ^1 H NMR, 13 C NMR and GPC. In vitro degradation rates of the three polymers PHDON, PBDON and PDON under different conditions were also investigated. Several copolymers P(BDON-co-DON)s were also synthesized.
关 键 词:5-苄氧甲基-1 4-二氧六环-2-酮 5-羟甲基-1 4-二氧六环-2-酮 开环聚合 聚(5-苄氧甲基-1 4-二氧六环-2-酮) 聚(5-羟甲基-1 4-二氧六环2-酮)
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