Abstract
In synthesizing chlorine-terminated telechelic polyisobutylene (PIB) with a p-DCCCp-dichlorocumene/BCl3/CH2Cl2 system, it is found that cycloalkylation occurs parallel with propagation. The factors leading to cycloalkylation were investigated in detail, to clarify its origin, to define its effects upon the molecular parameters of the polymer produced and to find ways to suppress it. It is found that cycloalkylation drastically influences MW, MWD and functionality of the polymer produced. High temperature, high medium polarity, low monomer concentration and the order of addition of BCl3 and p-DCC are the main factors favoring cycloalkylation.
Similar content being viewed by others
References
J.P.Kennedy and R.A.Smith, J.Polym. Scin., Polym. Chem. Ed., 18, 1523 (1980).
A. Fehervart, J.P.Kennedy, and F.Tudos, Polym. Prepr., 20(2), 320 (1979).
A. Fehervart, J.P.Kennedy, J. Macronol. Sci., Chem., A15(2), 215 (1980).
Wu Guanying, Chen Bin, Zhao Yixin, Polym. Bull, in press.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Guanying, W., Bin, C. & Yixin, Z. The synthesis of chlorine-terminated telechelic polyisobutylene. Polymer Bulletin 20, 221–228 (1988). https://doi.org/10.1007/BF00261972
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00261972