Polymerization of 9-(2,3-epoxypropyl)carbazole (EPC) and 1,2-epoxy-6-(
9-carbazolyl)-4-oxahexane (ECOH) with triphenylearbenium hexachloroant
imonate and triphenylcarbenium tetrafluoroborate have been studied by
the microoalorimetric technique. Triphenylcarbenium salts have turn ou
t to be more efficient catalyst for the polymerization of carbazolyl-c
ontaining epoxides than Lewis acids, giving high yields at low initial
concentration of the catalyst. Using comparatively restricted conditi
ons of reaction ([triphenylcarbenium salt]o greater-than-or-equal-to 0
.02 mol/l, t greater-than-or-equal-to 50-degrees-C) transition from th
e conventional active chain end mechanism to the activated monomer mec
hanism has been observed at a sufficiently high degree of conversion o
fmonomer.