Zhang Jinghan, Wu Yibo, Chen Kaixuan, Zhang Min, Gong Liangfa, Yang Dan, Li Shuxin, Guo Wenli
College of Material Science and Engineering, Beijing University of Chemical Technology, Beijing 100029, China.
Beijing Key Lab of Special Elastomeric Composite Materials, Beijing 102617, China.
Polymers (Basel). 2019 Mar 14;11(3):500. doi: 10.3390/polym11030500.
Aqueous cationic polymerizations of vinyl ethers (isobutyl vinyl ether (IBVE), 2-chloroethyl vinyl ether (CEVE), and -butyl vinyl ether (-BVE)) were performed for the first time by a CumOH/B(C₆F₅)₃/Et₂O initiating system in an air atmosphere. The polymerization proceeded in a reproducible manner through the careful design of experimental conditions (adding initiator, co-solvents, and surfactant or decreasing the reaction temperature), and the polymerization characteristics were systematically tested and compared in the suspension and emulsion. The significant difference with traditional cationic polymerization is that the polymerization rate in aqueous media using B(C₆F₅)₃/Et₂O as a co-initiator decreases when the temperature is lowered. The polymerization sites are located on the monomer/water surface. Density functional theory (DFT) was applied to investigate the competition between H₂O and alcohol combined with B(C₆F₅)₃ for providing a theoretical basis. The effectiveness of the proposed mechanism for the aqueous cationic polymerization of vinyl ethers using CumOH/B(C₆F₅)₃/Et₂O was confirmed.
首次在空气氛围中,通过CumOH/B(C₆F₅)₃/Et₂O引发体系进行了乙烯基醚(异丁基乙烯基醚(IBVE)、2-氯乙基乙烯基醚(CEVE)和丁基乙烯基醚(-BVE))的水相阳离子聚合反应。通过精心设计实验条件(添加引发剂、共溶剂和表面活性剂或降低反应温度),聚合反应以可重复的方式进行,并在悬浮液和乳液中对聚合特性进行了系统测试和比较。与传统阳离子聚合的显著差异在于,以B(C₆F₅)₃/Et₂O作为共引发剂时,水相介质中的聚合速率在温度降低时会下降。聚合位点位于单体/水表面。应用密度泛函理论(DFT)研究了H₂O和醇与B(C₆F₅)₃之间的竞争,从而提供了理论依据。证实了所提出的使用CumOH/B(C₆F₅)₃/Et₂O进行乙烯基醚水相阳离子聚合反应机理的有效性。