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作 者:GAO Long-cheng PAN Qi-wei FAN Xing-he CHEN Xiao-fang WAN Xin-hua ZHOU Qi-feng
机构地区:[1]College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, P. R. China [2]Key Laboratory of Polymer Chemistry and Physics of Ministry of Education, Bering 100871, P. R. China
出 处:《Chemical Research in Chinese Universities》2005年第5期615-618,共4页高等学校化学研究(英文版)
基 金:Supported by the National Natural Science Foundation of China(No. 20134010) ;the Science Research Fund of the Minis-try of Education of P. R. China(No. 104005).
摘 要:Bifunctional alkoxyamine bis-TIPNO derived from 2,2,5-trimethyl-4-phenyl-3-azahexane-3-oxyl (TIPNO) and α, ω-alkyl bromide by atom transfer radical addition(ATRA) was employed as “biradical initiator” for nitroxide-mediated radical polymerization(NMRP) of isoprene and styrene. The kinetics study for the polymerization of styrene at different time showed living features. The poly(styrene-b-isoprene-b-styrene) (SIS) copolymers have two glass transition temperatures, indicating the immiscibility of the corresponding blocks.Bifunctional alkoxyamine bis-TIPNO derived from 2,2,5-trimethyl-4-phenyl-3-azahexane-3-oxyl (TIPNO) and α, ω-alkyl bromide by atom transfer radical addition(ATRA) was employed as “biradical initiator” for nitroxide-mediated radical polymerization(NMRP) of isoprene and styrene. The kinetics study for the polymerization of styrene at different time showed living features. The poly(styrene-b-isoprene-b-styrene) (SIS) copolymers have two glass transition temperatures, indicating the immiscibility of the corresponding blocks.
关 键 词:Radical polymerization Block copolymer NITROXIDE ISOPRENE
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