Living cationic polymerization of styrene by the bifunctional initiating system 1,4-bis(1-chloroethyl)benzene/SnCl4 in the presence of 2,6-di-tert-butylpyridine

✍ Scribed by Oh-Sig Kwon; Chang Gi Gho; Byong-Seok Choi; Sam-Kwon Choi

• Publisher: John Wiley and Sons
• Year: 1994
• Tongue: English
• Weight: 393 KB
• Volume: 195
• Category: Article
• ISSN: 1022-1352
• DOI: 10.1002/macp.1994.021950625

✦ Synopsis

Abstract

The polymerization of styrene was studied by using a bifunctional initiator, 1,4‐bis(1‐chloroethyl)benzene (1). It was demonstrated that living polymerization can be achieved in the styrene/1/SnCl~4~ system in chloroform at −15°C in the presence of 2,6‐di‐tert‐butylpyridine. The number‐average molecular weight of the obtained polymers increases with monomer conversion and with addition of a fresh feed of monomer at the end of the first‐stage polymerization. The molecular weight distribution (MWD) of the obtained polymers is narrow ratio of weight‐ to number‐average molecular weights (M~w~/M~n~ < 1,2) throughout the polymerization. In the absence of 2,6‐di‐tert‐butylpyridine, the initiating system results polystyrene with a bimodal MWD. Also a bimodal MWD was obtained with H~2~O/SnCl~4~ as initiating system. 2,6‐Di‐tert‐butylpyridine in conjunction with H~2~O/SnCl~4~ does not lead to polymerization.