Chen Jian-Zhuang, Cui Kun, Zhang Shu-Yuan, Xie Peng, Zhao Qiao-Ling, Huang Jin, Shi Li-Ping, Li Guang-Yu, Ma Zhi
Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, P.R. China; Department of Chemistry, Zhengzhou University, Zhengzhou 450052, P.R. China.
Macromol Rapid Commun. 2009 Apr 1;30(7):532-8. doi: 10.1002/marc.200800683. Epub 2009 Feb 10.
Well-defined polymethylene-block-polystyrene (PM-b-PS) diblock copolymers were synthesized via a combination of living polymerization of ylides and atom transfer radical polymerization (ATRP) of styrene. A series of hydroxyl-terminated polymethylenes (PM-OHs) with different molecular weight and narrow molecular weight distribution were prepared using living polymerization of ylides following efficient oxidation in a quantitive functionality. Then, the macroinitiators (PM-MIs ($\overline M _{\rm n}$ = 1 900-15 000; PDI = 1.12-1.23)) transformed from PM-OHs in ≈ 100% conversion initiated ATRPs of styrene to construct PM-b-PS copolymers. The GPC traces indicated the successful extension of PS segment ($\overline M _{\rm n}$ of PM-b-PS = 5 000-41 800; PDI = 1.08-1.23). Such copolymers were characterized by (1) H NMR and DSC.
通过叶立德的活性聚合与苯乙烯的原子转移自由基聚合(ATRP)相结合的方法,合成了结构明确的聚亚甲基-嵌段-聚苯乙烯(PM-b-PS)二嵌段共聚物。在定量官能团中进行高效氧化后,利用叶立德的活性聚合制备了一系列具有不同分子量且分子量分布窄的羟基封端聚亚甲基(PM-OHs)。然后,由PM-OHs转化而来的宏观引发剂(PM-MIs($\overline M _{\rm n}$ = 1 900 - 15 000;PDI = 1.12 - 1.23))以约100%的转化率引发苯乙烯的ATRP反应,从而构建PM-b-PS共聚物。凝胶渗透色谱(GPC)曲线表明PS链段成功得到延长(PM-b-PS的$\overline M _{\rm n}$ = 5 000 - 41 800;PDI = 1.08 - 1.23)。此类共聚物通过(1)H NMR和DSC进行表征。