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作 者:CHEN Min CHEN Xiaonong YUAN Xinhua ZHANG Yan ZHANG Chunyan LIU Hua DAI Qixun
机构地区:[1]College of Chemical Engineering,Jiangsu University,Zhenjiang 212013,China [2]College of Material Science and Engineering,Jiangsu University,Zhenjiang212013,China
出 处:《Chinese Journal of Reactive Polymers》2006年第2期108-114,共7页中国反应性高分子(英文版)
基 金:National Natural Science Foundation of China (No. 20207003)
摘 要:To obtain new functional aromatic polymer materiul. 3,3'-biacenaphthene, which is used as macromolecule intermediate of,funcrion aromatic polymer material, was synthesized through the coupling reaction of acenaphthene catalyzing by ionic liquid ([bmim]CI/FeCl3) at mild reaction condition. Pure 3,3'-biacenaphthene was obtained hy recrystalling and column chromatography from the reaction mixture and was determined by GC/MS, SHNMR arid FTIR analysis. The influence of various reaction conditions on the yield of 3,3'-biacenaphthene were studied by GC analysis. The result shows that the optimun synthesis conditions of the coupling reaction are, as following: the molar ratio of FeCl3 to [BmimlCl being 3, the mole ratio of FeCl3 in [Bmim]Cl/FeCl3 to acenaphthene being 4. the reaction temperamre being 20 ℃ the reaction time being 4h and the solvent of the reaction system being PhNO2 Under those conditions, the yield of the 3.3'-biacenaphthene will be 48.71% and selectivity, of that will be 78.56 %. Farther more, [bmim]Cl/FeCl3 has no pollution to environments and can be reused.To obtain new functional aromatic polymer material, 3,3’-biacenaphthene, which is used as macromolecule intermediate of function aromatic polymer material, was synthesized through the coupling reaction of acenaphthene catalyzing by ionic liquid ([bmim]Cl/FeCl3) at mild reaction condition. Pure 3,3’-biacenaphthene was obtained by recrystalling and column chromatography from the reaction mixture and was determined by GC/MS, 1HNMR and FTIR analysis. The influence of various reaction conditions on the yield of 3,3’-biacenaphthene were studied by GC analysis. The result shows that the optimum synthesis conditions of the coupling reaction are as following: the molar ratio of FeCl3 to [Bmim]Cl being 3, the mole ratio of FeCl3 in [Bmim]Cl/FeCl3 to acenaphthene being 4, the reaction temperature being 20 ℃, the reaction time being 4h and the solvent of the reaction system being PhNO2. Under those conditions, the yield of the 3,3’-biacenaphthene will be 48.71 % and selectivity of that will be 78.56 %. Further more, [bmim]Cl/FeCl3 has no pollution to environments and can be reused.
关 键 词:Functional macromolecule intermediate 3 3'-biacenaphthene Synthesis Coupling reactions Ionic liquid CATALYZE
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