A series of main-chain Liquid-crystalline ionomers containing sulfonate gro
ups pendant on the polymer backbone were synthesized by an interfacial cond
ensation reaction of 4,4'-dihydroxy-alpha,alpha'-dimethyl benzalazine, a me
sogenic monomer, with brilliant yellow (BY), a sulfonate-containing monomer
, and a 1/9 mixture of terephthaloyl and sebacoyl dichloride. The structure
s of the polymers were characterized by LR and UV spectroscopies. DSC and t
hermogravimetric analysis were used to measure the thermal properties of th
ose polymers, and the mesogenic properties were characterized by a polarize
d optical microscope, DSC, and wide-angle X-ray diffraction. The ionomers w
ere thermally stable to about 310 degreesC. They were thermotropic liquid-c
rystalline polymers (LCPs) with high mesomorphic-phase transition temperatu
res and exhibited broad nematic mesogenic regions of 160-170 degreesC, and
they were lyotropic LCPs with willowy leaf-shaped textures in sulfuric acid
. However, the thermotropic liquid-crystalline properties were somewhat wea
kened because the concentration of BY was more than 8%. The inherent viscos
ity in N-methyl-2-pyrrolidone suggested that intramolecular associations of
sulfonate groups occurred at low concentration, and intermolecular associa
tions predominated at higher concentration. (C) 2001 John Wiley & Sons, Inc
.