窄分子量分布双亲性嵌段共聚物PEO-b-PtBA的合成及其水解窄分子量分布双亲性嵌段共聚物PEO-b-PtBA的合成及其水解
doi: 10.3969/j.issn.1000-5641.2015.03.014
Synthesis of amphiphilic copolymer PEO-b-PtBA with narrow molecular weight distribution and its hydrolysis
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摘要: 以PEO-Br为大分子引发剂,通过ATRP法合成了一组两亲性两嵌段共聚物PEO45-b-PtBAx(x=28, 35, 53).采用HNMR、FTIR、 SEC和TEM对产物进行了表征,讨论了投料比对控制产物的分子链结构,分子量及其分布的影响.结果表明,tBA的转化率较高,1H NMR结果显示成功制得目标产物,所得嵌段共聚物均具有极窄的分子量分布(Mw/Mn1.07).在tBA相对于PEOBr的投料比较小时可以对嵌段共聚物结构进行精确调控.tBA投入量的增大会导致分子量分布变宽及引发效率下降.PEO45-b-PtBA35被成功水解为PEO45-b-PAA35,在中性水溶液中PEO45-b-PAA35自组装形成了分散较为均匀的球形胶束.Abstract: A group of amphiphilic diblock copolymers PEO45-b-PtBAx(x=28, 35, 53) were synthesized by ATRP using PEO-Br as macroinitiator. Samples were characterized by SEC, 1H NMR, FTIR and TEM. The influence of feed ratio to the control of the structure, molecular weight and molecular weight distributions were discussed. The results showed that, the conversion of tBA was high and the 1H NMR results confirmed the targeted products were synthesized successfully. All three copolymers had a narrow molecular weight distributions (Mw/Mn1.07). When the feed ratio of tBA to PEOBr was low, the structures of copolymers could be controlled accurately. The increase of feed ratio of tBA to PEOBr caused broadening of molecular weight distributions and the decreasing of initiating efficiency. The hydrolysis of PEO45-b-PtBA35 to PEO45-b-PAA35 was performed successfully. PEO45-b-PAA35was selfassembled into well dispersed spherical micelles in neutral aqueous solution.
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Key words:
- amphiphilic copolymerATRPPEO-PtBAhydrolysis /
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