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Fast and convenient synthesis of amine-terminated polylactide as a macroinitiator for ω-benzyloxycarbonyl-L-lysine-N-carboxyanhydrides  ( EI收录)  

文献类型:期刊文献

英文题名:Fast and convenient synthesis of amine-terminated polylactide as a macroinitiator for ω-benzyloxycarbonyl-L-lysine-N-carboxyanhydrides

作者:Ju, Mingjie[1]; Gong, Feirong[1]; Cheng, Shujun[1]; Gao, Yun[1]

机构:[1] Key Laboratory for Ultrafine Materials of Ministry of Education, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China

年份:2011

卷号:2011

外文期刊名:International Journal of Polymer Science

收录:EI(收录号:20214511124951)

语种:英文

外文关键词:Ring opening polymerization - Molecular weight

摘要:Amine-terminated poly (L-lactide) (NH2-PLLA) with various chain lengths were successfully synthesized by sequential tert-butyl-N-(3- hydroxypropyl) carbamate initiated bulk ring-opening polymerization (ROP) of L-lactide (L-LA) in the presence of Stannous(II) 2-ethylhexanoate (Sn(Oct) 2) and deprotection of the N-tert-butoxycarbonyl (Boc) group at the end of the polymer chain. The polymers obtained were characterized by FT-IR, 1H NMR, and GPC method. NH2-PLLA thus prepared was used to initiate the polymerization of ω-benzyloxycarbonyl-L-lysine-N- carboxyanhydride (Lys (Z)-NCA), and the result confirmed the high nucleophilicity of the terminal amine group. This method was not only suitable for the preparation of low molecular weight NH2-PLLA, but also quite efficient in the synthesis of high molecular weight samples. Copyright ? 2011 Mingjie Ju et al.

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