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A set of short-tailed discotic liquid crystals are presented which feature a mesophase despite having methoxy units as tails. Their unusual properties are a result of strategic fluorination, with more fluorination leading to broader mesophase ranges. 

Abstract Manipulating light is an important area of optical research and development. To that end, tunable dichroic devices in which the reflectivity at differing wavelengths can be adjusted, are particularly valuable. This work is motivated by recent studies of the optical properties of chiral ferroelectric nematic liquid crystals (FNLCs). Here electro‐optical studies are presented on two room temperature, FNLC materials that demonstrate electrically tunable reflectivity when subject to a field below 0.2 V µm⁻¹. Moreover, under appropriate conditions, the reflectivity can also be electrically (and reversibly) tuned (without change of color) from 0% to 40%. Reversible, low voltage tunable mirrors, having miniscule power consumption and operable around ambient temperature are expected to be useful in diverse applications ranging from energy‐saving, smart windows to virtual reality interfaces. 

We present discotic liquid crystals consisting of fluorinated triphenylene with unusually short tails, including mere methoxy or ethoxy tails. Understanding these short-tailed liquid crystals may lead to new applications for discotic liquid crystals. 

Abstract The dynamics of swimming bacteria depend on the properties of their habitat media. Recently it is shown that the motion of swimming bacteria dispersed directly in a non‐toxic water‐based lyotropic chromonic liquid crystal can be controlled by the director field of the liquid crystal. Here, we investigate whether the macroscopic polar order of a ferroelectric nematic liquid crystal (N_F) can be recognized by bacteria B. Subtilis swimming in a water dispersion adjacent to a glassy N_Ffilm by surface interactions alone. Our results show that B. Subtilis tends to move in the direction antiparallel to the spontaneous electric polarization at the N_Fsurface. Their speed is found to be the same with or without a polar N_Flayer. In contrast to observation on crystal ferroelectric films, the bacteria do not get immobilized. These observations may offer a pathway to creation of polar microinserts to direct bacterial motion in vivo. 

The isotropic to ferroelectric nematic liquid transition was theoretically studied over one hundred years ago, but its experimental studies are rare. Here we present experimental results and theoretical considerations of novel electromechanical effects of ferroelectric nematic liquid crystal droplets coexisting with the isotropic melt. We find that the droplets have flat pancake-like shapes that are thinner than the sample thickness as long as there is room to increase the lateral droplet size. In the center of the droplets a wing-shaped defect with low birefringence is present that moves perpendicular to a weak in-plane electric field, and then extends and splits in two at higher fields. Parallel to the defect motion and extension, the entire droplet drifts along the electric field with a speed that is independent of the size of the droplet and is proportional to the amplitude of the electric field. After the field is increased above 1 mV μm −1 the entire droplet gets deformed and oscillates with the field. These observations led us to determine the polarization field and revealed the presence of a pair of positive and negative bound electric charges due to divergences of polarization around the defect volume. 

Liquid crystal properties of compounds with a variety of polar terminal groups including cyano, fluoro, isothiocyanato, etc., were studied well, however, not enough attention was given to nitro terminal compounds. In this work, a series of fluorine tail terminated alkoxy nitrobiphenyl compounds were synthesised and their mesogenic properties were analysed. In addition, the simple alkoxy nitrobiphenyl compounds were synthesised and analysed in order to compare them with fluoro-alkoxy nitrobiphenyl compounds and for binary mixture analysis. Fluorine tail termination to the alkoxy chain does suppress the smectic phase that was observed for the simple alkoxy nitrobiphenyl compounds with longer chains. Fluorine tail terminated alkoxy nitrobiphenyl compounds with longer chains (C7-C10) show monotropic nematic phase around ambient temperature and supercooling properties and these compounds are useful for a binary mixture analysis. Moreover, computation and experimental analyses of the alkoxy nitrobiphenyl compounds were performed to investigate the potential use of these nitro terminal compounds as chemoresponsive liquid crystal materials. 

A new synthetic approach for fluorinated alkoxytriphenylene discotic liquid crystals is presented. This methodology exploits the previously described photocyclodehydrofluorination (PCDHF) reaction for the preparation of fluorinated triphenylene derivatives coupled with a variety of nucleophilic aromatic substitution (S N Ar) reactions. This particular combination of reactions provides a versatile route to discotic materials with carefully controlled core fluorine and alkoxy tail content. In the course of these studies, new discotic materials with minimal tail content have been revealed. The mesogenic properties of these materials are reported, and their charge transport properties are measured using the time of flight technique. 

Computational methods can provide first-principles insights into the thermochemistry and kinetics of reactions at interfaces, but this capability has not been widely leveraged to design soft materials that respond selectively to chemical species. Here we address this opportunity by demonstrating the design of micrometer-thick liquid crystalline films supported on metal-perchlorate surfaces that exhibit selective orientational responses to targeted oxidizing gases. Initial electronic structure calculations predicted Mn 2+ , Co 2+ , and Ni 2+ to be promising candidate surface binding sites that (1) coordinate with nitrile-containing mesogens to orient liquid crystal (LC) phases and (2) undergo redox-triggered reactions upon exposure to humid O 3 leading to a change in the strength of binding of the nitrile group to the surface. These initial predictions were validated by experimental observations of orientational transitions of nitrile-containing LCs upon exposure to air containing parts-per-billion concentrations of O 3 . Additional first-principles calculations of reaction free energies of metal salts and oxidizing gases predicted that the same set of metal cations, if patterned on surfaces at distinct spatial locations, would provide LC responses that allow Cl 2 and O 3 to be distinguished while not responding to environmental oxidants such as O 2 and NO 2 . Experimental results are provided to support this prediction, and X-ray diffraction measurements confirmed that the experimentally observed LC responses can be understood in terms of the relative thermodynamic driving force for formation of MnO 2 , CoOOH, or NiOOH from the corresponding metal cation binding sites in the presence of humid O 3 and Cl 2 . 

The development of responsive soft materials with tailored functional properties based on the chemical reactivity of atomically precise inorganic interfaces has not been widely explored. In this communication, guided by first-principles calculations, we design bimetallic surfaces comprised of atomically thin Pd layers deposited onto Au that anchor nematic liquid crystalline phases of 4′- n -pentyl-4-biphenylcarbonitrile (5CB) and demonstrate that the chemical reactivity of these bimetallic surfaces towards Cl 2 gas can be tuned by specification of the composition of the surface alloy. Specifically, we use underpotential deposition to prepare submonolayer to multilayers of Pd on Au and employ X-ray photoelectron and infrared spectroscopy to validate computational predictions that binding of 5CB depends strongly on the Pd coverage, with ∼0.1 monolayer (ML) of Pd sufficient to cause the liquid crystal (LC) to adopt a perpendicular binding mode. Computed heats of dissociative adsorption of Cl 2 on PdAu alloy surfaces predict displacement of 5CB from these surfaces, a result that is also confirmed by experiments revealing that 1 ppm Cl 2 triggers orientational transitions of 5CB. By decreasing the coverage of Pd on Au from 1.8 ± 0.2 ML to 0.09 ± 0.02 ML, the dynamic response of 5CB to 1 ppm Cl 2 is accelerated 3X. Overall, these results demonstrate the promise of hybrid designs of responsive materials based on atomically precise interfaces formed between hard bimetallic surfaces and soft matter.