We report the synthesis and liquid crystalline properties of a new type of tribranched compound built up from triazine as the central core and electron-rich triazine rings as peripheral groups. An equimolar mixture of the star-shaped compound based on the 1,3,5-triazine core with 4-dodecyloxybenzoic acid produced an organic salt exhibiting a columnar mesophase with a dendritic growing texture at low temperatures. The liquid crystalline properties of the triazine-based compound and organic salt were investigated by differential scanning calorimetry and polarizing optical microscopy.

A new six-armed compounds consist of benzene ring as a central core substituted with aromatic ring and three rod-like armed of 2-chloro-4,6-bis(dodecyloxy)-1,3,5-triazine as the peripheral arms unit which obtained by sequential nucleophilic substitution of chlorine atoms in cyanuric chloride. The substitution took place at the acetylenic periphery on the central benzene ring by Sonogashira coupling. Equimolar mixtures of the six-armed compounds based on the benzene core with the complementary 4-dodecyloxybenzoic acid, which already possessed liquid crystal property, resulted in an organic salt. The organic salts and structures were investigated by differential scanning calorimetry (DSC), and confirmed by spectroscopic methods (1H-NMR, 13C-NMR and Mass spectroscopy)

In this study, we reported the synthesis of a new tribranched macromolecule liquid crystal with triazine in the centre. The central triazine core is bonded via sequences of Sonigashira coupling to 3 triazine unites through acetylenic bridges. The triazines at the periphery are substituted with 2 chiral citronellyloxy side groups. The salt of the resulting star-shaped macromolecule, which was oily at room temperature, with 4-dodecyloxybenzoic acid at 1:1 ratio exhibited a Smectic C (SmC) mesophase. The liquid crystalline properties of organic salt were investigated using DSC (differential scanning calorimetry) and POM (polarizing optical microscopy).

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