We take 5,6,11,12,17,18-hexaaztrinaphthylene and dibenzo[a,c]phenazine as our central core that with dove-tailed side chains. It is shown that the size-related increase of steric interactions among the peripheral side chains substituted to the aromatic core leads to a dramatically lowered isotropization temperature.

The dibenzo[a,c]phenazine dimers with the branched alkoxy chain of disc were synthesized simplely. We now show on the synthesis of this series of compounds which were found to exhibit mesomorphism as determined by polarized optical microscopy (POM), differential scanning calorimetry (DSC) and X-ray diffraction (XRD). These materials showed polymeso- morphism and glass formation. In our investigations, we also observed that the effects of branched chains on dibenzo[a,c]phenazine enhanced columnar liquid crystal phase stability indeed.

Discotic liquid crystals (DLC) have been reported with a large number of discoid cores to improve the degree of intermolecular ordering because the liquid crystals own to self-assembly into columnar stacking and self¡Vhealing ability. In my research, a series of disc-like £k-conjugated molecules based on aromatic rigid cores have been newly synthesized. I focus on the hexaazatrinaphthylene (HATN) and dibenzo-[a,c]- phenazine as aromatic cores, changing different side chains to control the mesomorphic behavior and their supermolecular assembly.