“…Generally, lateral substitution decreases the thermal stability of both solid and mesophases [1][2][3][4][5][6]. Supramolecular liquid crystals are frequently induced, through hydrogen bonding, between aromatic carboxylic acids, as proton donor, and pyridine-based components, as proton acceptor [7][8][9][10][11][12][13][14][15]. We have previously reported [16][17][18] the preparation and characterization of some supramolecular, hydrogen-bonded, complexes between derivatives of pyridylazophenyl substituted benzoates (as proton-acceptors) and 4-alkoxybenzoic acids (as the proton donors).…”