The self-assembly of a rod-coil amphiphilic block copolymer (ABCP) led to Im3‾ m and Pn3‾ m polymer cubosomes and p6mm polymer hexasomes. This is the first time that these structures are observed in a rod-coil system. By varying the hydrophobic chain length, the initial concentration of the polymer solution, or the solubility parameter of the mixed solvent, head-tail asymmetry is adjusted to control the formation of polymer cubosomes or hexasomes. The formation mechanism of the polymer cubosomes was also studied. This research opens up a new way for further study of the bicontinuous and inverse phases in different ABCP systems.
The large-area formation of functional micropatterns with liquid crystals is of great significance for diversified applications in interdisciplinary fields. Meanwhile, the control of molecular alignment in the patterns is fundamental and prerequisite for the adequate exploitation of their photoelectric properties. However, it would be extremely complicated and challenging for discotic liquid crystals (DLCs) to achieve the goal, because they are insensitive to external fields and surface chemistry. Herein, a simple method of patterning and aligning DLCs on flat substrates is disclosed through precise control of the formation and dewetting of the capillary liquid bridges, within which the DLC molecules are confined. Large-area uniform alignment occurs spontaneously due to directional shearing force when the solvent is slowly evaporated and programmable patterns could be directly generated on desired substrates. Moreover, the in-plane column direction of DLCs is tunable by slightly tailoring their chemical structures which changes their self-assembly behaviors in liquid bridges. The patterned DLCs show molecular orientation-dependent charge transport properties and are promising for templating self-assembly of other materials. The study provides a facile method for manipulation of the macroscopic patterns and microscopic molecular orientation which opens up new opportunities for electronic applications of DLCs.
A polynorbornene-based mesogen-jacketed liquid crystalline polymer (MJLCP) containing polyhedral oligomeric silsesquioxane (POSS) in the side chain, PNb10POSS, was synthesized through ring-opening metathesis polymerization. The chemical structure of the monomer was confirmed by 1 H/ 13 C NMR, high-resolution mass spectrometry, and elemental analysis. Molecular characterizations on the polymer were performed with 1 H NMR, gel permeation chromatography, and thermogravimetric analysis. The phase behavior of this new organic-inorganic hybrid polymer was investigated by differential scanning calorimetry, 2 polarized light microscopy, one-dimensional wide-angle X-ray scattering, synchrotron-radiation SAXS, two-dimensional wide-angle X-ray diffraction, and high-resolution transmission electron microscopy. With the competitive self-assemblies of the two covalently connected building blocks, namely MJLCP and POSS moieties, PNb10POSS shows various phase structures including an angstrom POSS crystal (Cr), a hexagonal columnar (Col h ) phase and the Cr coexisting, and the Col h phase at different temperatures. The POSS crystal has a tremendous effect on the liquid crystalline (LC) behavior of the MJLCP. The results show that the competition between the crystallization of POSS and the LC formation of the polymer as a whole results in the complex phase behavior of the MJLCP-based nanohybrid. The polymer self-assembles into an organic-inorganic hybrid inclusion complex on the sub-10 nm scale. This work provides a new approach for the design and synthesis of ordered structures constructed by self-assembly on the sub-10 nm scale.
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