Liquid crystals are unique in their properties and use and has an essential role in the area of technological applications such as electrical, optical, displayers, temperature maps, and switching materials. This study aimed to synthesize hexaethynylbenzene derivatives starting from 1,3,5-trichlorobenzene benzene as a central core substituted with three aromatic ring and three armed of 2-chloro-4,6-bis((3,7-dimethyloct-6-en-1-yl) oxy)-1,3,5-triazine. These molecules are formed by the covalent linking of three arms symmetrically to a central core which may be attached to the central core through flexible, semi-flexible or rigid linkers. The substitution occured at the acetylenic periphery on the central benzene ring and was achieved efficiently by Sonogashira coupling. The six-armed compounds based on the benzene core was mixed with the complementary 4-dodecyloxybenzoic acid 1:1 ratio, which already possessed liquid crystal property to increase the formation of these resulting in an organic salt. The obtained organic salts were investigated for their liquid crystal behaviour by polarizing optical microscopy (POM) and differential scanning calorimetry (DSC). All the intermediate and final compounds were confirmed by spectroscopic techniques (1H NMR, 13C NMR, and mass spectrometry).
Synthesis and Liquid Crystal Property of 4,5-Disubstituted Phenanthrene and 9,10-Dihydrophenanthrene Derivatives
