Dk. Moon et al., SYNTHESIS OF POLY(1-AMINONAPHTHALENE) AND POLY(1-AMINOANTHRACENE) BY CHEMICAL OXIDATIVE POLYMERIZATION AND CHARACTERIZATION OF THE POLYMERS, Macromolecules, 26(25), 1993, pp. 6992-6997
Poly(1-aminonaphthalene) and poly(1-aminoanthracene) have been synthes
ized in high yields (90-96%) by chemical oxidative polymerization of 1
-aminonaphthalene and 1-aminoanthracene using H2O2 in the presence of
Fe catalyst. The oxidative polymerization of 1-aminonaphthalene and 1-
aminoanthracene proceeds via successive coupling that gives the polyme
r structure similar to polyaniline. The polymers are brown powders and
soluble in dimethyl sulfoxide (DMSO), dimethylformamide (DMF), N-meth
yl-2-pyrrolidone (NMP), H2SO4, and HCOOH. The obtained poly(1-aminonap
hthalene) and poly(1-aminoanthracene) show electrical conductivities o
f 1.7 X 10(-6) and 1.6 x 10(-4) S cm-1, respectively, which increase t
o 3.8 X 10(-4) 1.5 X 10(-3) S cm-1 on doping with HCl or I2. Light sca
ttering measurement of the polymers in NMP shows a large degree of dep
olarization (rho(v) = 0.33), indicating that the polymers have a linea
r and stiff structure. The number-average molecular weights (M(n)) of
poly(1-aminonaphthalene) and poly(1-aminoanthracene) obtained are dete
rmined as 4300 and 4500, respectively, with narrow molecular weight di
stribution by gel permeation chromatography (vs polystyrene). The weig
ht-average molecular weight (M(w)) of poly(1-aminoanthracene) determin
ed by the light scattering method is 7000. H-1 NMR spectra of PNA and
PAA in DMSO-d6 give rise to the absorption of the NH hydrogen in the r
egion of delta 5-6 ppm, and the NH hydrogen of PNA is exchangeable wit
h the water hydrogen contained in DMSO-d6 on the NMR time scale with a
n activation energy of 27 kJ mol-1. PNA and PAA do not show a distinct
absorption peak in the visible region.