Abstract
Thermal and mesomorphic properties of possible 1:1 supramolecular complexes (SMCs) (I-m/I-n) designed from two members of 4-[(4-(n-alkoxy)phenylimino)methyl]benzoic acid with symmetrical or un-symmetrical alkoxy terminal flexible chains (carbons of m and n = 6, 8 and 16), were analyzed by differential scan-calorimetry (DSC), thermogravemetric (TG) analysis, and their mesophases identified by polarized optical microscopy (POM). The equimolecular mixtures of the two acids possess symmetrical and un-symmetrical terminal lengths. The mesomorphic properties of the binary mixtures were examined as a function of the total alkoxy chain length on both sides. Results revealed that the nematic mesophase temperature range increases as the total terminal length increases for all designed un-symmetrical mixtures. A comparison was constructed between the formed SMCs and of those of the previously prepared 4-n-alkoxyphenylazo benzoic acids as well as the 4-n-alkoxy benzoic acids, to examine the impact of mesogenic core on the mesomorphic properties. The comparison indicated that as the mesogenic portion lengthens the thermal mesophase stability exhibits higher values of phase transition temperatures; whereas, the azo and Schiff base moieties exhibited near thermal properties.