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作 者:Hui Peng Wan-li Chen Jie Kong Zhi-quan Shen 凌君
机构地区:[1]MOE Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University [2]Center of Analysis & Measurement, Zhejiang University of Technology [3]Shaanxi Key Laboratory of Macromolecular Science and Technology, School of Science, Northwestern Polytechnical University
出 处:《Chinese Journal of Polymer Science》2014年第6期743-750,共8页高分子科学(英文版)
基 金:financially supported by the National Natural Science Foundation of China(No.21174122);Special Funds for Major Basic Research Projects(No.G2011CB606001);Zhejiang Provincial Natural Science Foundation of China(No.Y4110115)
摘 要:It is reported that alkali-metal borohydrides (MBH4, M = Li, Na and K) are efficient catalysts for ring opening polymerization (ROP) of α-amino acid N-carboxyanhydrides (NCAs). Polypeptides are prepared in quantitative yields with relatively narrow molecular weight distributions (MWDs = 1.1-1.5) which depend on the reaction temperature. End groups of the produced polypeptide are studied in detail by MALDI-ToF MS, IH-NMR, 13C-NMR, IH-1H COSY and IH-13C HMQC analyses. The results indicate that α-hydroxy-ω-aminotelechelic polypeptides are formed which are suitable for post- polymerization functionalization.It is reported that alkali-metal borohydrides (MBH4, M = Li, Na and K) are efficient catalysts for ring opening polymerization (ROP) of α-amino acid N-carboxyanhydrides (NCAs). Polypeptides are prepared in quantitative yields with relatively narrow molecular weight distributions (MWDs = 1.1-1.5) which depend on the reaction temperature. End groups of the produced polypeptide are studied in detail by MALDI-ToF MS, IH-NMR, 13C-NMR, IH-1H COSY and IH-13C HMQC analyses. The results indicate that α-hydroxy-ω-aminotelechelic polypeptides are formed which are suitable for post- polymerization functionalization.
关 键 词:POLYPEPTIDE Alkali-metal borohydride α -Amino acid N-carboxyanhydride End group functionalization.
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