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Synthesis of fulleropyrrolidines through the reaction of [60]fullerene with quaternary ammonium salts and amino acids
Authors:Bo Jin  Ru-Fang Peng  Juan Shen  Shi-Jin Chu
Institution:aDepartment of Chemistry, Southwest University of Science and Technology, Mianyang 621010, China;bSchool of Chemical Engineering and Environment, Beijing Institute of Technology, Beijing 100081, China;cAnalytical & Testing Center, Sichuan University, Chengdu 610064, China
Abstract:The reactions of 60]fullerene with amino acids and quaternary ammonium salts in toluene afforded two fulleropyrrolidine derivatives. One fulleropyrrolidine derivative contained a RCH moiety originating from quaternary ammonium salts through C–N bond cleavages and other fulleropyrrolidine derivatives contained a PhCH moiety originating from toluene through C–H bond cleavage. By using chlorobenzene instead of toluene as solvent, only one fulleropyrrolidine derivative containing a RCH moiety was obtained in the reactions.
Keywords:Fullerene  Amino acids  Cycloaddition reaction  Quaternary ammonium salts
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