A series of copolymers were synthesized by chemically oxidative polymerizat
ion of pyrrole (PY) and m-toluidine (MT) in hydrochloride aqueous medium at
ambient temperature. The yield, intrinsic viscosity, and solubility of the
copolymers were studied by changing PY/MT molar ratio from 0/100 to 88/12.
The as-prepared PY/MT copolymer bases were characterized by FT-IR. UV-VIS,
H-1 NMR, DSC, and wide-angle X-ray diffraction. The results suggested that
the oxidative polymerization from pyrrole and m-toluidine is exothermic an
d the resulting copolymers are more easily soluble in most of the organic s
olvents than polypyrrole. The polymer obtained is a real copolymer containi
ng pyrrole and m-toluidine units, but the PY content calculated on the basi
s of the proton NMR spectra is lower than feed PY content. (C) 2001 Elsevie
r Science B.V. All rights reserved.