Mesomorphic behaviour of N,N '-dialkanoyl-3,4,5,6-tetramethylbenzene-1,2-diamines and related compounds

DSC, X-ray, broad-line proton NMR, and microscopy studies on several series of N,N-dialkanoylbenzene-1,2-diamines are presented. The melting point and associated enthalpy are not much affected by methylation of the aromatic n ucleus. While the dimethyl compounds carrying heptanoyl-to-hexadecanoyl gro ups generate metastable mesophases below 111 degreesC, the 3,4,5,6-tetramet hyl compounds carrying propionyl-to-hexadecanoyl groups produce stable hexa gonal columnar mesophases appearing mostly above 200 degreesC. N,N'-dialkyl benzene-1,2-carboxamides are transformed into birefringent viscous fluids e xhibiting a focal-conic texture at a temperature between 76 and 99 degreesC when the alkyl groups are decyl, undecyl, dodecyl, and tetradecyl.