化工进展

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烷氧基团在聚碳酸酯合成反应中的活性

孙建正,周宏勇,李云庆,王小梅,王家喜   

  1. 河北工业大学化工学院,天津 300130
  • 出版日期:2011-09-05 发布日期:2011-09-05

Reaction activity of alkyloxy group in synthesis of polycarbonate

SUN Jianzheng,ZHOU Hongyong,LI Yunqing,WANG Xiaomei,WANG Jiaxi   

  1. School of Chemical Engineering,Hebei University of Technology,Tianjin 300130,China
  • Online:2011-09-05 Published:2011-09-05

摘要:

采用碳酸酯(二甲酯二乙酯二正丙酯二异丙酯及二正丁酯)与1,6-己二醇反应制备不同端基的碳酸酯齐聚物,产物结构分析表明,碳酸二甲酯及碳酸二正丁酯的反应活性较高,碳酸二正丙酯碳酸二乙酯及碳酸二异丙酯的反应活性相近。结合不同封端的齐聚碳酸酯与乙二醇反应产物的核磁共振分析,碳酸酯中烷氧基的反应活性顺序为:甲氧基>丁氧基>丙氧基>乙氧基>异丙氧基。同时,讨论了酯交换反应的可能机理。

Abstract:

The carbonates with different terminal groups were synthesized by transesterification of 1,6-hexanediol and dimethyl carbonatediethyl carbonatedipropyl carbonatediisopropyl carbonatedibutyl carbonaterespectively. Based on the analysis of productsthe activities of dimethyl carbonate and dibutyl carbonate were higherwhile the activities of diethyl carbonatedipropyl carbonatediisopropyl carbonate were similar. Referring to the NMR analysis of products of carbonate oligomer with different end group with glycerolthe activity of alkyloxy group in carbonate was in the orderMeO> BuO>PrO> EtO>i-PrO. The possible mechanism of the transesterification was proposed.

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