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首页> 外文期刊>Macromolecular symposia >Anionic Synthesis of α-Functionalized Polymers by Combination of 1,1-Diphenylethylene and Hydrosilation Chemistry
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Anionic Synthesis of α-Functionalized Polymers by Combination of 1,1-Diphenylethylene and Hydrosilation Chemistry

机译:1,1-二苯基乙烯与硅氢化反应的阴离子合成α-官能化聚合物

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摘要

A new general anionic functionalization method (GFM) for preparing α-chain-end functionalized polymers utilizes the initiator formed from sec-butyllithium and dimethyl[4-(1-phenylvinyl)-phenyl]silane (DPESiH) followed by hydrosilation with substituted alkenes. α-(4-dimethylsilyl hydride)phenyl-functionalized polystyrene and poly(methyl methacrylate) were synthesized in quantitative yield by living anionic polymerization. These α-silyl hydride-functionalized polymers were further functionalized by reaction with tridecafluorooctene in the present of Karstedt's hydrosilation catalyst. These tridecafluorooctane-functionalized polymers were characterized by SEC, FTIR, ~1H-, ~(13)C- and ~(19)F-NMR spectroscopy.
机译:一种用于制备α-链端官能化聚合物的新型通用阴离子官能化方法(GFM),该方法利用了由仲丁基锂和二甲基[4-(1-苯基乙烯基)-苯基]硅烷(DPESiH)形成的引发剂,然后与取代的烯烃进行硅氢化反应。通过活性阴离子聚合以定量收率合成了α-(4-二甲基甲硅烷基氢化物)苯基官能化的聚苯乙烯和聚(甲基丙烯酸甲酯)。通过在Karstedt的氢化硅烷化催化剂的存在下与十三氟辛烯反应,将这些α-甲硅烷基氢化物官能化的聚合物进一步官能化。这些十三氟辛烷官能化的聚合物通过SEC,FTIR,〜1H-,〜(13)C-和〜(19)F-NMR光谱进行了表征。

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