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线性聚(环氧乙烷)-嵌段-聚(环氧丙烷)-嵌段-聚(ε-己内酯)(PEO-PPO-PCL)共聚物的合成、表征及自组装。

Synthesis, characterization, and self-assembly of linear poly(ethylene oxide)-block-poly(propylene oxide)-block-poly(ε-caprolactone) (PEO-PPO-PCL) copolymers.

机构信息

College of Science, China University of Petroleum, 66 West Changjiang Road, Qingdao, Shandong 266580, PR China.

出版信息

J Colloid Interface Sci. 2013 Mar 1;393:174-81. doi: 10.1016/j.jcis.2012.10.051. Epub 2012 Nov 8.

Abstract

Amphiphilic triblock copolymers of PEO-PPO-PCL with various block compositions have been synthesized by ring-opening polymerization (ROP) of ε-caprolactone (ε-CL) initiated by the OH group of methoxy-poly(ethylene oxide)-poly(propylene oxide) (Me-PEO-PPO). Their structures were confirmed by Fourier transform infrared (FT-IR) measurements, and their self-assembly in aqueous solution was studied using fluorescence spectroscopy, transmission electron microscopy (TEM), UV-vis spectra, differential scanning calorimetry (DSC), and surface tension. For the copolymers studied in this paper, the critical aggregation concentrations (CAC) ranged from 5×10(3) to 2 mg/L. The critical micelle concentrations (CMC) decreased with increasing PCL block length, and the downtrend was more significant in the short PCL block length. All of the three copolymers were capable of solubilizing hydrophobic molecules (pyrene) in aqueous solution and copolymers with a longer PCL block exhibited a stronger solubilizing ability. The TEM images showed that the size and morphology of the aggregations could be tuned by varying the compositions or the concentration.

摘要

具有不同嵌段组成的 PEO-PPO-PCL 两亲性嵌段共聚物已通过由甲氧基聚(环氧乙烷)-聚(环氧丙烷)(Me-PEO-PPO)的 OH 基团引发的ε-己内酯(ε-CL)的开环聚合(ROP)合成。它们的结构通过傅里叶变换红外(FT-IR)测量得到证实,并且通过荧光光谱法、透射电子显微镜(TEM)、紫外-可见光谱、差示扫描量热法(DSC)和表面张力研究了它们在水溶液中的自组装。对于本文研究的共聚物,临界聚集浓度(CAC)范围为 5×10(3)至 2mg/L。临界胶束浓度(CMC)随 PCL 嵌段长度的增加而降低,在短 PCL 嵌段长度下下降趋势更为明显。所有三种共聚物都能够在水溶液中溶解疏水分子(芘),并且具有较长 PCL 嵌段的共聚物表现出更强的溶解能力。TEM 图像表明,可以通过改变组成或浓度来调节聚集物的大小和形态。

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