A series of new liquid crystalline compounds with BCH- and CBC- structures
was synthesized. They differ from the known carbocyclic analogs by the 1,2,
4-oxadiazole fragment placed in various positions of the long mesomorphic m
olecule. The cross-coupling reaction of the aromatic boric acids and bromid
es is a new way for mesogenic heterocycles design. The transition temperatu
res of these new liquid crystals are lower as compared with carbocyclic BCH
- and CBC- analogs and significantly depend on the position of the nonlinea
r heterocyclic unit in the molecular chain.