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首页> 外文期刊>Polymer: The International Journal for the Science and Technology of Polymers >Synthesis of biocompatible tadpole-shaped copolymer with one poly(ethylene oxide) (PEO) ring, two poly(ε-caprolactone) (PCL) tails by combination of glaser coupling with ring-opening polymerization
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Synthesis of biocompatible tadpole-shaped copolymer with one poly(ethylene oxide) (PEO) ring, two poly(ε-caprolactone) (PCL) tails by combination of glaser coupling with ring-opening polymerization

机译:通过玻璃偶联与开环聚合反应合成具有一个聚环氧乙烷(PEO)环,两个聚ε-己内酯(PCL)尾巴的生物相容性pole形共聚物

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摘要

The biocompatible tadpole-shaped copolymers [cyclic-poly(ethylene oxide) (PEO)]-b-[linear poly(ε-caprolactone) (PCL)] _2 [(c-PEO)-b-PCL _2] with one PEO ring and two PCL tails were synthesized by combination of glaser coupling with ring-opening polymerization (ROP). First, a linear PEO precursor with two alkyne groups at the chain terminal and two hydroxyl groups at the chain middle was prepared by ROP of EO monomer and the following transformation of functional groups. Then, cyclic PEO with two hydroxyl groups at the same site was obtained by the "Glaser" cyclization. Finally, the hydroxyl groups on cyclic PEO directly initiated the ROP of ε-CL monomer to produce the target copolymers (c-PEO)-b-PCL _2. The target copolymers and intermediates were all well characterized by GPC, MALDI-TOF MS, ~1H NMR and FT-IR.
机译:具有一个PEO环的生物相容性t形共聚物[环状-聚环氧乙烷(PEO)]-b- [线性聚(ε-己内酯)(PCL)] _2 [(c-PEO)-b-PCL _2]并通过玻璃偶联和开环聚合(ROP)合成了两条PCL尾巴。首先,通过EO单体的ROP和随后的官能团转化,制备了在链末端具有两个炔基并且在链中间具有两个羟基的线性PEO前体。然后,通过“ Glaser”环化获得在相同位置具有两个羟基的环状PEO。最后,环状PEO上的羟基直接引发了ε-CL单体的ROP,从而生成了目标共聚物(c-PEO)-b-PCL _2。目标共聚物和中间体均通过GPC,MALDI-TOF MS,〜1H NMR和FT-IR进行了很好的表征。

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