高等学校化学学报 ›› 2000, Vol. 21 ›› Issue (S1): 473.
• Synthetic Sciences • 上一篇 下一篇
LU Jiang, LIANG Hui, LI Bao-En
LU Jiang, LIANG Hui, LI Bao-En
摘要:
The living cationic polymerization of β-pinene was carried out with α-chloroethylbenzene(PEC)/TiCl4/Ti(OiPr)4 initiating system in CH2C12 at -40℃. After 25 min of reaction(β-pinene conversion~100%),the resulted living poly(β-pinene) was capped with a few units of styrene and then the polymerization was quenched to give β-pinene macroinitiator with benzenyl chloride chain end (P(β-p)-St-Cl). The structure of the macroinitiator was confirmed by 1H NMR (Fig.l). The macroinitiator, in conjunction with AgSbF6 or AgC1O4,was used to initiate the ring-opening cationic polymerization of THF in the presence of propylene oxide promoter. GPC analysis of the obtained polymers showed that AgSbF6 system led to almost pure block copolymers of β-pinene with THF, whereas AgC1O4 system gave mixtures of block copolymers and low molecular weight homopolymers of THF and unreacted macroinitiator (Fig.2). 1H NMR analysis further confirmed the formation of β-pinene/THF block copolymers with macroinitiaor/AgSbF6 system (Fig.3).
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