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Synthesis of cyclic polystyrene via a combination of intramolecular coupling and ATRP
Authors:Xu?Hua?Shi,Hai?Tao?Xu,Tao?Yan,Ri?Wen?Yu,Yin?Peng?Xu,Han?Jia?Chen  author-information"  >  author-information__contact u-icon-before"  >  mailto:hjchen@stu.edu.cn"   title="  hjchen@stu.edu.cn"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) School of Science, Shantou University, Shantou, 515063, China;(2) Analytical and Testing Center, Shantou University, Shantou, 515063, China;
Abstract:Cyclic polystyrene with narrow molecular weight distribution was synthesized by intramolecular coupling of α-carboxyl-ω-butylamino heterotelechelic polystyrene using 2-chloro-1-methylpyridinium and triethylamine as the catalyst in highly dilute solution. The linear precursor α-carboxyl-ω-butylamine polystyrene was first prepared by atom transfer radical polymerization using 4-(chloromethyl)benzoic acid as the initiator and followed by nucleophilic substituted with n-butylamine. The results of IR, 1H NMR, and gel permeation chromatography revealed that highly pure cyclic polystyrene was synthesized via a combination of intramolecular coupling and atom transfer radical polymerization, and can be isolated easily by column chromatography on silica gel using ethyl acetate as the eluant.
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