Spontaneous Helix Formation in Non-Chiral Bent-Core Liquid Crystals with Fast Linear Electro-Optic Effect

Liquid crystals (LCs) represent one of the foundations of modern communication and photonic technologies. Present display technologies are based mainly on nematic LCs, which suffer from limited response time for use in active colour sequential displays and limited image grey scale. Herein we report the first observation of a spontaneously formed helix in a polar tilted smectic LC phase (SmC phase) of achiral bent-core (BC) molecules with the axis of helix lying parallel to the layer normal and a pitch much shorter than the optical wavelength. This new phase shows fast (∼30 μs) grey-scale switching due to the deformation of the helix by the electric field. Even more importantly, defect-free alignment is easily achieved for the first time for a BC mesogen, thus providing potential use in large-scale devices with fast linear and thresholdless electro-optical response. les

Formation and Development of Nanometer-sized Cybotactic Clusters in Bent-core Nematic Liquid Crystalline Compounds

Two homologue achiral bent-core liquid crystals (LCs), BCN66 and BCN84, in their nematic phases are studied by dielectric spectroscopy in the frequency range 10 Hz–10 MHz. In each of these compounds, two relaxation processes are identified and assigned to (i) collective dynamics of molecules in nanometer-sized cybotactic clusters and (ii) individual molecular relaxations, in the ascending order of frequency of the probe field. The temperature and the bias electric field dependence of the dielectric strength and relaxation frequency for these processes are shown to give rise to sharpness in cluster boundaries, increased size and volume fraction in the LC nematic phase. The effect of the bias field on the LC cell is similar to reducing its temperature; both variables increase the cluster size and volume fraction and give rise to sharp cluster boundaries. The findings confirm that dielectric spectroscopy is a powerful and an extremely useful technique to provide a deeper understanding of the mechanism of cybotactic cluster formation in the isotropic liquid and the nematic phase of LCs as a function of temperature and the bias field

Non-symmetric ether-linked liquid crystalline dimers with a highly polar end group

<p>A new class of non-symmetric dimeric compounds derived from 4-cyano-4′-hydroxybiphenyl in which two rigid parts are connected via flexible spacers have been designed and synthesised. These materials possess trialkoxy chains attached at one end of the molecule, while the other end consists of a biphenyl moiety terminated with the highly polar cyano group. The molecular structures of these dimers have been confirmed by elemental analysis and spectroscopic data and their phase behaviour has been characterised by differential scanning calorimetry (DSC) and polarizing optical microscopy (POM). Almost all of the synthesised materials exhibit liquid crystalline properties depending on the number of carbon atoms in the terminal chains, where all short chains derivatives form nematic phases and depending on the length of the internal spacer long terminal chains homologues display crystalline or unidentified smectic phase.</p

Tailor-designed polyphilic promotors for stabilizing dispersions of carbon nanotubes in liquid crystals

We present a potent multifunctional molecular design concept for promoting the dispersion of carbon nanotubes (CNTs) in thermotropic liquid crystals (LCs), making CNT-in-LC dispersions of unprecedented stability possible and broadening the scope of potential applications

Synthesis of New U-Shaped Azobenzene Liquid Crystals for Photoswitching Properties

A new series of liquid crystalline compounds comprising a U-shaped unit as central core incorporating azobenzene in the side arms and having terminal alkene functional groups, is synthesized and characterized by differential scanning calorimetry (DSC), polarized-light optical microscopy (POM), X-ray diffraction analysis and UV-vis spectroscopy. In the U-shaped series, all compounds showed stable enantiotropic monolayer SmA phases independent on the chain length and chain parity. These U-shaped molecules exhibit strong photoisomerisation behaviour in solutions and in solid state. The photoswitching properties of compounds showed trans to cis isomerization in about 15 seconds, whereas reverse process required much longer times ranging from 235–380 min in solutions. In case of solid film of 4a, E–Z photoisomerization takes around 4 s and the reverse transformation to original Z–E state takes about 74 min. The kinetic study using UV light irradiation shows that all compounds (4a–e) behave first order rate law throughout the relaxation time in solution. The effect of alkyl chain length for trans to cis is negligible whereas, cis to trans is substantial on the odd–even chain length. The photoisomerization study with variable light intensities shows that the photosaturation and thermal back relaxation times are decreased when intensity of the irradiated light is increased. Compounds did not degrade with light illumination at 10 mW cm−2. The reversible isomerization did not significantly decay after multiple cycles indicating that the photo-responsive properties are stable and repeatable. Thus, the photoswitching behaviour of these materials may be suitably exploited in the field of optical data storage device and in molecular switches for suitable switching times

Polyphilic hydrogen bonded block molecules involving semiperfluorinated and silylated molecular fragments

2,4-Diamino-6-phenyl-1,3,5-triazines grafted with one or two semiperfluorinated chains at the phenyl substituent have been investigated in binary mixtures with one-chain and two-chain oligo(dimethylsiloxy) terminated 4-alkoxy- and 3,4-dialkoxybenzoic acids. Equimolar mixtures of the triazines with the complementary acids form discrete double hydrogen-bonded heterodimers with an elongated central core. Mesomorphic properties are observed only if at least two terminal fluoroalkyl chains are attached to the triazine entity. Three to four heterodimers generate aggregates with preferably parallel adjusted rod-like H-bonded cores. The space requirement of the segregated peripheral fluoroalkyl and oligosiloxane segments considerably exceeds that of the central core region, leading to an overall circular geometry of the associates which organize in columnar LC phases. The chains initiate a local segregation which is however not long range and retains a time and space averaged two-dimensional hexagonal lattice

Cybotactic nematic phases of photoisomerisable hockey-stick liquid crystals

<p>New five-ring hockey-stick liquid crystalline materials with 4-bromoresorcinol as the central core unit and an azobenzene-based side arm were synthesised and their mesophase behaviour was investigated by polarising optical microscopy, differential scanning calorimetry, X-ray diffraction and under a triangular wave electric field. Additional structural modification was done by introducing a lateral fluorine atom in the terminal ring of one of the side arms. It is found that regardless of the alkyl chain length or the lateral fluorine substitution, all of the prepared materials are liquid crystalline exhibiting nematic phases composed of cybotactic clusters of the SmC-type (N_CybC) in addition to a monotropic SmC phase for the longest homologue.</p