A new mesogenic monomer was prepared from biphenyl-3,3',4,4' -tetracarboxyl
ic dianhydride and 4-aminophenol followed by the acylation of OH groups wit
h propionic anhydride. This diphenol propionate was polycondensed by transe
sterification with decane-1,10-dicarboxylic acid, dodecane-1,12-dicarboxyli
c acid, and eicosane-1,20-dicarboxylic acid or with equimolar mixtures of t
wo dicarboxylic acids. The resulting poly(ester imide)s were characterized
by elemental analyses, H-1 NMR spectra, inherent viscosities, DSC measureme
nts, optical microscopy, and X-ray measurements with synchrotron radiation
at variable temperatures. An enantiotropic smectic A phase in the molten st
ate and a crystalline smectic E (or H) phase in the solid state were found
in all cases. (C) 2000 John Wiley & Sons, Inc.