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A unique gyroid cubic phase has been discovered for a discotic star mesogen with three covalently attached DNA bases. In this cubic Ia3‾d ${Ia\bar{3}d}$ phase, the conjugated core of the mesogens and the thymine pseudo guests self‐assemble in mirror image continuous networks, representing a semiconducting material with three‐dimensional transport pathways. The hole carrier mobilities are found to be in the typical range of poly(phenylenevinylene) scaffolds. This structure is stabilized by a weak hydrogen bonding between the thymine bases and can be switched to a columnar liquid crystal – thermally and by the addition of complementary adenine guests. [ABSTRACT FROM AUTHOR]

Shape‐persistent conjugated mesogens with oligothiophene arms of different lengths have been synthesized. Such mesogens possess free intrinsic space between their conjugated arms. They form columnar liquid‐crystalline phases, in which the void is filled by dense helical packing in the neat phase similar to an oligo(phenylene vinylene) derivative of equal size. The void can also be compensated by the inclusion of the small acceptor molecule 2,4,7‐trinitrofluorenone. In solution, the acceptor interacts with the core as the largest π‐surface, while in the solid material, it is incorporated between the arms and sandwiched by the star‐shaped neighbours along the columnar assemblies. The TNF acceptors are not nanosegregated from the star‐shaped donors, thus the liquid crystal structure converts to a nano‐reservoir for TNF (endo‐receptor). These host–guest arrangements are confirmed by comprehensive X‐ray scattering experiments and solid‐state NMR spectroscopy. This results in ordered columnar hexagonal phases at high temperatures, which change to helical columnar mesophases or to columnar soft crystals at room temperature. [ABSTRACT FROM AUTHOR]

We report the H-type self-aggregation of a new linear water-soluble BODIPY bolaamphiphile equipped with amide groups and oligoethylene glycol chains. Intermolecular π-π interactions, amide-based hydrogen bonds and hydrophobic interactions lead to a highly cooperative self-assembly process. Detailed spectroscopic studies suggest that strong hydrophobic interactions are the driving force for a rotational displacement of the dye molecules within the stack in order to shield the hydrophobic π-system from water molecules. The so formed highly-ordered micellar structures have been further characterized by NMR, AFM, TEM, DLS studies and theoretical calculations. [ABSTRACT FROM AUTHOR]

The self‐assembly of umbrella‐shaped mesogens is explored with subphthalocyanine cores and oligo(thienyl) arms with different lengths in the light of their application as light‐harvesting and photoconducting materials. While the shortest arm derivatives self‐assemble in a conventional columnar phase with a single mesogen as a repeating unit, the more extended derivatives generate dimers that pile up into liquid crystalline columns. In contrast to the antiparallel arrangement known from single crystals, the present mesogens align as parallel dimers in polar columnar phases as confirmed by X‐ray scattering, experimental densities, dielectric spectroscopy, second harmonic generation, alignment, and conductivity studies. UV–vis and fluorescence spectroscopies reveal a broad absorption in the visible range and only weak emission of the Q‐band. Thus, these light‐collecting molecules forming strongly polar columnar mesophases are attractive for application in the area of photoconductive materials. [ABSTRACT FROM AUTHOR]