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
Os. Kwon et al., 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, Macromolecular chemistry and physics, 195(6), 1994, pp. 2187-2194
The polymerization of styrene was studied by using a bifunctional init
iator, 1,4-bis(1-chloroethyl)benzene (1). It was demonstrated that liv
ing polymerization can be achieved in the styrene/l/SnCl4 system in ch
loroform at - 15-degrees-C in the presence of 2,6-di-tert-butylpyridin
e. The number-average molecular weight of the obtained polymers increa
ses with monomer conversion and with addition of a fresh feed of monom
er 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)BAR/M(n)BAR < 1,2) througho
ut the polymerization. In the absence of 2,6-di-tert-butylpyridine, th
e initiating system results polystyrene with a bimodal MWD. Also a bim
odal MWD was obtained with H2O/SnCl4 as initiating system. 2,6-Di-tert
-butylpyridine in conjunction with H2O/SnCl4 does not lead to polymeri
zation.