The only two series of carboxylic acids, 3-nitro- or 3-cyano-4-alkoxybiphen
yl-4-carboxylic acid, are known to exhibit the optically isotropic phase (S
ID). Now we synthesised 4-(branched alkoxy)-anilinebenzylidene-4'-carboxyli
c acid series, all being racemic, and investigated their mesophase properti
es by means of DSC, optical microscopy and X-ray measurement. A, a result,
some branched azomethine derivatives were found to form a SD phase. We also
synthesised cinnamic acid derivatives with branched alkoxy tail that were
turned out to exhibit either SD phase or hexagonal columnar phase. We tried
biphenyl or azobenzene core analogues which were found to produce a highly
ordered smectic phase or no mesophase, respectively. At this stage, we sup
pose it plays an important role that the branch is introduced into the term
inal chain and a certain dipole moment is located within the mesogenic core
. These factors may allow the peculiar molecular packing that causes an opt
ically isotropic property.