Self-assembled “supra-molecular” liquid-crystalline phases were investigated in one of a series of symmetrically tapered bisamides based on an amide core of 1,2-bis[3,4,5-tris(alkan-1-yloxy)benzamido]benzene and three alkyl tails on each side of the core. One of this series of bisamides having 14 carbon atoms in each tail (abbreviated as C 14 PhBA) served as an example in this study. Differential scanning calorimetry thermal diagrams showed two main phase transition processes in C 14 PhBA. Wide-angle X-ray diffraction results revealed that the high-temperature phase transition is between the isotropic melt (I) and a 2D low-ordered oblique columnar phase (I ↔ Φ OB ). The low-temperature phase transition was attributed to the transition between a highly ordered, oblique columnar (Φ OK ) phase and the Φ OB phase. Supra-molecular columns were directly visualized using transmission electron microscopy and atomic force microscopy. The formation of these supra-molecular structures is critically dependent upon the construction of building blocks (“columns”) by C 14 PhBA molecules. These building blocks developed via rigid amide core/alkyl tail micro-phase separation and the hydrogen (H) bond formation between the N−H and carbonyl groups among the cores. Spectroscopic studies showed that the columns were stabilized by intercore H-bonds oriented along the column long axis, and the alkyl tails in the Φ OK phase were packed into an ordered mesophase having about 64% of the methylene carbon atoms in long trans segments at room temperature. In the Φ OB phase, the alkyl tails adopt liquidlike disordered conformations. The high- and low-temperature phase transitions were thus mainly attributed to the sudden changes in H-bonding and alkyl tail conformation, respectively. A detailed packing model of the Φ OK phase was proposed and qualitatively proven using a simulated structural diffraction.
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Xue et al. (2004) studied this question.
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