I. Mav et M. Zigon, Synthesis and NMR characterization of a novel polyaniline derivative - Thecopolymer of 2-methoxyaniline and 3-aminobenzenesulfonic acid, POLYM BULL, 45(1), 2000, pp. 61-68
The synthesis and solution-state NMR investigation of the structure of a no
vel type of water-soluble polyaniline (PANI) derivative in leucoemeraldine
and emeraldine oxidation states is presented. Copolymers of 3-aminobenzenes
ulfonic acid and 2-methoxyaniline (PMAOMA) with various monomer molar ratio
s were synthesized by chemical polymerization in a hydrochloric acid medium
. Due to a large difference in the reactivities of 2-methoxyaniline (OMA) a
nd 3-aminobenzenesulfonic acid (MA), the content of OMA in the copolymers w
as much higher (over 0.65 of the mole fraction) than in the reaction mixtur
e. Structural characterization of the reaction products was performed using
one- (H-1, C-13) and two-dimensional (GHSQC and GCOSY) NMR spectroscopy. T
he NMR data indicated an almost block structure of OMA sequences of variabl
e length separated by shorter sequences of MA units. It was also shown that
the incorporation of MA units in the copolymer chains favors the formation
of a less oxidized material.