Chem. J. Chinese Universities ›› 2000, Vol. 21 ›› Issue (S1): 473.

• Synthetic Sciences • Previous Articles     Next Articles

Synthesis of β-Pinene/THF Block Copolymers

LU Jiang, LIANG Hui, LI Bao-En   

  1. Department of Polymer and Material Science, Zhongshan University, Guangzhou 510275
  • Online:2000-12-31 Published:2000-12-31
  • Supported by:

    Financial support given by National Natural Science Foundation of China (29874040), and Specialty Foundation for Excellent Young Teachers of the Education Department of China, is gratefully acknowledged.

Abstract:

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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