A Photomechanical Film in which Liquid Crystal Design Shifts the Absorption into the Visible Light Range.

Liquid crystalline polymer networks (LCN) with azobenzene monomers bend reversibly under UV-light irradiation, combining photomechanical and photothermal effects. However, the harmful nature of UV-light limits their use in biology and soft robotics. Although visible light-absorbing tetra-ortho-fluoro-substituted azobenzenes exist, liquid crystalline monomers have never been prepared. Previously, such azobenzenes were added as photoactive additives (up to 10%) to otherwise passive liquid crystalline polymer networks. In this work, a molecular design of a liquid crystalline, polymerizable azobenzene switchable by visible light is presented. The monomer assembles in a highly fluid nematic phase, but polymerizes in a layered smectic C phase. The films are produced solely from the monomer without additional liquid crystalline components and are actuated with visible light. Bending experiments in air and under water differentiate photomechanical and photothermal effects. Remarkably, a 60 µm splay aligned film maintains its deformation for hours, slowly reverting over days. Monomer liquid crystallinity is characterized using differential scanning calorimetry (DSC), wide-angle X-ray scattering (WAXS), and polarized optical microscopy (POM); polymer films are analyzed using WAXS and DSC on a homogeneously aligned film. The synthetic procedure is high yielding and polymer film fabrication is scalable, which enables the use of safe and efficient photomechanical LCNs in soft robotics, engineering and biology.

From molecular biaxiality of real board-shaped mesogens to phase biaxiality? On the hunt for the holy grail of liquid crystal science.

In the search of the predicted biaxial nematic phase, a series of shape-persistent board-shaped mesogens with maximum molecular biaxiality and a dipole along the minor molecular axis were designed to form nematic (N) mesophases. One compound exhibits a wide nematic temperature range, which can be supercooled to room temperature. A comprehensive variable temperature X-ray study on aligned samples reveals patterns being dominated by the form factor of very small aggregates, from which the aspect ratio of the lead compound with length (L) : breadth (B) : width (W) of 10.73 : 3.16 : 1.23 could be obtained. The ratio is close to the predicted optimum molecular biaxiality by Straley's hard particle model. Hence variable temperature proton relaxation studies on this mesogen were carried out over a wide frequency range. The global fit of the frequency dispersions at five temperatures with a motional model requires in addition to the usual rotation/reorientation contribution, two independent director fluctuations contributions: one for the conventional nematic order director (n) fluctuations and the other for the minor director (m) fluctuations (normal to n). The correlation length of the minor directors determined by NMR could extend to 5-8 molecules in the W direction, but only to the nearest neighbour in the B direction, as found by X-ray diffraction. Both X-ray and NMR studies indicate that these new types of lead structure are extremely promising to find the long sought-after biaxial N mesophase.

Fullerene-Filled Stilbene Stars: The Balance between Isolated C60 Helices and 3D Networks in Liquid-Crystal Self-Assemblies.

A series of shape-persistent star-shaped oligo(phenylene vinylene) liquid crystals and derivatives with fullerene tethered through spacers of different lengths to one arm were successfully synthesized. Solution studies by NMR, UV/Vis and fluorescence spectroscopy revealed the preferential location of the C60 acceptor in the vicinity of the peripheral donor unit, which affects the quenching of the emission of the conjugated stilbenoid scaffold in the donor-acceptor dyad. The fluorescence was completely absent in the liquid crystal phase due to the extraordinary hierarchical self-assembly. In this family of mesogens, the intrinsic free space has to be filled either by an extremely tight packing of the stars or by the fullerenes as guests. The spacer lengths control the nanosegregation of the C60 units in the cavities of the stars in either independent triple helices or unprecedented 3D networks, in which fullerenes are positioned at the interface of neighboring columns. Eventually, the clearing temperature of such large complex donor-acceptor systems can be tuned by an entropy effect defined by the length of the spacer. The accessibility of the isotropic phase without decomposition is an important prerequisite for future alignment studies associated with potential material applications in organic electronics.