Liquid-crystalline circularly polarised fluorescent emitters with a high luminescence dissymmetry factor.

Chiral liquid-crystalline emitters based on 9,9-dimethyl-10-(4-(phenylsulfonyl)phenyl)-9,10-dihydroacridine and a functionalised binaphthol show smectic liquid crystal phases and circularly polarised blue fluorescence with a high luminescence dissymmetry factor |glum| of 0.13. Solution-processable organic light-emitting diodes (OLEDs) based on the enantiomers were explored.

Liquid-crystalline circularly polarised TADF emitters for high-efficiency, solution-processable organic light-emitting diodes.

Achieving a high emission efficiency and a large luminescence asymmetry factor (glum) in a single molecule exhibiting circularly polarised thermally activated delayed fluorescence (CP-TADF) remains a formidable challenge. In this work, a proof-of-concept, liquid-crystalline CP-TADF molecule is proposed to realise high glum by taking advantage of the order inherent in liquid crystals. Employing a chiral dinaphthol-based CP-TADF molecule as the emissive unit, a pair of liquid-crystalline CP-TADF molecules (R/S-4) is synthesised via the introduction of six mesogenic moieties. The enantiomers show intense emission at about 520 nm which has clear TADF and liquid-crystalline characteristics. Both enantiomers display symmetrical electronic circular dichroism (CD) and circular polarisation luminescence (CPL) signals as thin films. Impressively, relatively large glum values of 0.11 are realised for the films. Solution-processed devices were fabricated using R/S-4 as the dopants, with the TADF molecule CzAcSF as the sensitiser. The OLEDs so prepared show a very high maximum external quantum efficiency of 21.2%, revealing a novel strategy for realising large glum values in CP-TADF.

Bioinspired Interfacial Spontaneous Growth of ZnO Nanocatalysts onto Recycled Textiles as a Sustainable Approach for Water Purification.

Zinc oxide, as a commonly used photocatalytic degradation of organic pollutants, typically shows limitations in wastewater treatment, such as aggregation and recycling problems caused by nanoscale dimensions and inappropriate substrates. Anchoring ZnO on substrates is a strategy to obtain stable catalytic performance. Particularly, natural fibers with hollow structures are an attractive alternative for ecological and economical ZnO loading templates, but depositing ZnO onto hollowed fiber surfaces presents a challenge. Here, a straightforward in situ growth method for producing nanostructured zinc oxide on cotton fibers from recycled garments is reported. The modified polydopamine on the fiber surface captures the catalyst required for in situ growth of ZnO and serves as a platform for spontaneous catalytic crystal growth on the fiber surface. The ZnO nanocrystals are uniformly dispersed on the outer and inner walls of cotton fibers, demonstrating excellent durability in wastewater treatments. Moreover, the photocatalytic performance of functional fibers is optimized by doping Ag nanoparticles to improve degradation efficiency. This can extend the prospect of further applications of developed ZnO/fibers in optoelectronics, spintronics, and provide inspiration for recycling and upgrading of used garments.

Selective Microwave-Assisted Pyrolysis of Cellulose towards Levoglucosenone with Clay Catalysts.

Levoglucosenone (anhydrosugar) is one of the most promising chemical platforms derived from the pyrolysis of biomass. It is a chiral building block for pharmaceuticals as well as an intermediate in the production of solvents and polymers. Therefore, the development of cost-efficient, low-energy production methods is vital for a future sustainable biorefinery. Here, a novel, green approach to the production of levoglucosenone was developed by using a microwave (MW)-assisted pyrolysis of cellulose in the presence of readily available clays. It was shown that natural and pillared clays in the presence of MW irradiation significantly increase the yield of levoglucosenone from cellulose. Both the water content and the presence of acid centres are critical characteristics that influence the yield and distribution of catalysed products. A unique experiment was designed by using a synergetic effect between different types of catalysts, which enhanced the levoglucosenone yield to 12.3 wt % with 63 % purity.

Efficiency improvements in a dichroic dye-doped liquid crystal Fresnel lens.

A dichroic dye-doped liquid crystal Fresnel lens was fabricated and investigated to observe the combination of phase and amplitude modulation based focusing. An anthraquinone dichroic dye was doped into a liquid crystal host, which when in the Fresnel lens configuration, generates a Fresnel zone plate with alternating "transparent" and "opaque" zones. The zones were induced by using photo-alignment of a light-sensitive alignment layer to generate the alternating pattern. The voltage dependency of efficiency for the dye-doped and pure liquid crystal Fresnel devices were investigated. Incorporation of dyes into the device yielded a significant 4% improvement in relative efficiency in the lens, giving a maximum of 37% achieved in the device, much closer to the theoretical 41% limit when compared with the non-dye-doped device. The input polarization dependence of efficiency was also investigated, showing very small fluctuations (±1.5%), allowing further insight into the effect of fabrication method on these liquid crystal Fresnel devices.

Combined Microscopy, Calorimetry and X-ray Scattering Study of Fluorinated Dimesogens.

The material FDO11DFCB3 (compound 2 in this work) remains the only example of a liquid-crystalline material to exhibit a phase transition from the heliconical twist-bend phase into a lamellar smectic A mesophase, additionally this material exhibits a previously unidentified mesophase. We have prepared and characterised several homologues of this compound, with each material subjected to an in-depth analysis by optical microscopy, calorimetry and small angle X-ray scattering studies. Despite FDO11DFCB3 being similar in chemical structure to the novel materials presented herein its liquid-crystalline behaviour is rather different, indicating an unexpected sensitivity of the twist-bend phase to molecular structure.

Rational Design of Rod-Like Liquid Crystals Exhibiting Two Nematic Phases.

Recently, a polar, rod-like liquid-crystalline material was reported to exhibit two distinct nematic mesophases (termed N and NX ) separated by a weakly first-order transition. Herein, we present our initial studies into the structure-property relationships that underpin the occurrence of the lower-temperature nematic phase, and report several new materials that exhibit this same transformation. We have prepared material with significantly enhanced temperature ranges, allowing us to perform a detailed study of both the upper- and lower-temperature nematic phases by using small-angle X-ray scattering. We observed a continuous change in d spacing rather than a sharp change at the phase transition, a result consistent with a transition between two nematic phases, structures of which are presumably degenerate.

Photoswitching of Dihydroazulene Derivatives in Liquid-Crystalline Host Systems.

Photoswitches and dyes in the liquid-crystalline nematic phase have the potential for use in a wide range of applications. A large order parameter is desirable to maximize the change in properties induced by an external stimulus. A set of photochromic and nonphotochromic dyes were investigated for these applications. It was found that a bent-shaped 7-substituted dihydroazulene (DHA) photoswitch exhibited liquid-crystalline properties. Further investigation demonstrated that this material actually followed two distinct reaction pathways on heating, to a deactivated form by a 1,5-sigmatropic shift and to a linear 6-substituted DHA. In addition, elimination of hydrogen cyanide from the photoactive DHA gave both bent and linear azulene dyes. In a nematic host that has no absorbance around 350 nm, it was found that only the linear DHA derivative has nematic properties; however, both 6- and 7-substituted DHAs were found to have large order parameters. In the nematic host, ring opening of either DHA to the corresponding vinylheptafulvene resulted in a decrease in dichroic order parameter and an unusually fast back-reaction to a mixture of both DHAs. Likewise, only the linear azulene derivative showed mesomorphic properties. In the same nematic host, large order parameters were also observed for these dyes.

Principal molecular axis and transition dipole moment orientations in liquid crystal systems: an assessment based on studies of guest anthraquinone dyes in a nematic host.

An assessment of five different definitions of the principal molecular axis along which molecules align in a nematic liquid crystal system has been made by analysing fully atomistic molecular dynamics (MD) simulations of a set of anthraquinone dyes in the cyanobiphenyl-based nematic host mixture E7. Principal molecular axes of the dyes defined by minimum moment of inertia, minimum circumference, minimum area, maximum aspect ratio, and surface tensor models were tested, and the surface tensor model was found to give the best description. Analyses of MD simulations of E7 alone showed that the surface tensor model also gave a good description of the principal molecular axes of the host molecules, suggesting that this model may be applicable more generally. Calculated dichroic order parameters of the guest-host systems were obtained by combining the surface tensor analysis with fixed transition dipole moment (TDM) orientations from time-dependent density functional theory (TD-DFT) calculations on optimised structures of the dyes, and the trend between the dyes generally matched the trend in the experimental values. Additional analyses of the guest-host simulations identified the range of conformers explored by the flexible chromophores within the dyes, and TD-DFT calculations on corresponding model structures showed that this flexibility has a significant effect on the TDM orientations within the molecular frames. Calculated dichroic order parameters that included the effects of this flexibility gave a significantly improved match with the experimental values for the more flexible dyes. Overall, the surface tensor model has been shown to provide a rationale for the experimental alignment trends that is based on molecular shape, and molecular flexibility within the chromophores has been shown to be significant for the guest-host systems: the computational approaches reported here may be used as a general aid in the predictive design of dyes with appropriate molecular shapes and flexibilities for guest-host applications.

Experimental and molecular dynamics studies of anthraquinone dyes in a nematic liquid-crystal host: a rationale for observed alignment trends.

Five anthraquinone dyes with bis(4-propylphenyl) substituents, connected via sulfide or amine linking groups at the 1,5-positions or directly at the 2,6-positions, have been studied as guests in the nematic liquid crystal host, E7. Polarized UV-visible absorption spectra of aligned samples were used to obtain experimental dichroic order parameters, which exhibit values in the range 0.51-0.74. Fully atomistic MD simulations of these guest-host systems were carried out, generally using default parameters but using new force constants derived here for the dyes containing flexible phenyl-sulfide and phenyl-amine linking groups. An analysis of the alignment of the dye molecules in these simulations provides calculated molecular order parameters, which are combined with calculated order parameters for the alignment of the transition dipole moments within the dyes, reported previously, to give calculated dichroic order parameters. The trend in the calculated dichroic order parameters between the dyes shows a good match with the trend in the experimental values, enabling the observed variation to be rationalised primarily by changes in the alignment of the calculated transition dipole moments within the dyes; the calculated molecular order parameters show a relatively small variation between the dyes. The results indicate that this computational approach may be used generally to rationalise trends in the alignment of guest molecules in liquid crystal hosts, suggesting that it may also be able to provide a predictive aid in the design of guest dyes.

Blue and Green Phosphorescent Liquid-Crystalline Iridium Complexes with High Hole Mobility.

Blue- and green-emitting cyclometalated liquid-crystalline iridium complexes are realized by using a modular strategy based on strongly mesogenic groups attached to an acetylacetonate ancillary ligand. The cyclometalated ligand dictates the photophysical properties of the materials, which are identical to those of the parent complexes. High hole mobilities, up to 0.004 cm(2) V(-1) s(-1), were achieved after thermal annealing, while amorphous materials show hole mobilities of only approximately 10(-7) -10(-6) cm(2) V(-1) s(-1), similar to simple iridium complexes. The design strategy allows the facile preparation of phosphorescent liquid-crystalline complexes with fine-tuned photophysical properties.

Chiral dopants and the twist-bend nematic phase--induction of novel mesomorphic behaviour in an apolar bimesogen.

Herein we report studies on a bimesogen that exhibits a chiral twist bend nematic phase when doped with small weight percentages of a chiral material and a partial phase diagram constructed. At low concentrations a wide temperature range blue phase is observed, whereas at higher concentrations an additional 'nematic-like' mesophase was discovered at a lower temperature than the twist-bend nematic phase. In addition to an apparent isotropic-"isotropic" transition, the doped materials also exhibited a weakly birefringent phase upon annealing in the isotropic liquid phase, implying pretransitional behaviour in the same vein as that seen for TGB phases. When confined in a planar aligned cell, the NTB phase exhibited two domains that alternated between light and dark with rotation of the sample stage, as well as the application of an external electric field. Upon the addition of a chiral dopant one of these domains was eliminated, leading to their assignment as twist domains of opposite handedness.

Dyes in Liquid Crystals: Experimental and Computational Studies of a Guest-Host System Based on a Combined DFT and MD Approach.

Practical applications of guest-host liquid crystal systems are critically dependent on the alignment of the guest species within the liquid crystal host. UV/Vis absorption spectroscopy shows that the 1,5-dihydroxy-2,6-bis-(4-propylphenyl)-9,10-anthraquinone dye aligns within the E7 nematic host, giving an experimental dichroic ratio of 9.40 and dye order parameter of 0.74. This alignment was modelled by using a combination of density functional theory (DFT) and molecular dynamics (MD) computational approaches that do not require the input of experimental data. Time-dependent DFT calculations show that the electronic transition dipole moment is highly aligned with the long molecular axis of the dye. Fully atomistic MD simulations show that the long axis of the dye is less highly aligned within the E7 host, indicating that this contribution limits the overall dye alignment and, thereby, the potential practical applications of this particular system. Importantly, this study demonstrates an experimental and combined DFT and MD computational approach that may be applied generally to guest-host systems, providing a potential route to their rational design.

Apolar bimesogens and the incidence of the twist-bend nematic phase.

The nematic twist-bend phase (NTB) was, until recently, only observed for polar mesogenic dimers, trimers or bent-core compounds. In this article, we report a comprehensive study on novel apolar materials that also exhibit NTB phases. The NTB phase was observed for materials containing phenyl, cyclohexyl or bicyclooctyl rings in their rigid-core units. However, for materials with long (>C7) terminal chains or mesogenic core units comprising three ring units, the NTB phase was not observed and instead the materials exhibited smectic phases. One compound was found to exhibit a transition from the NTB phase to an anticlinic smectic C phase; this is the first example of this polymorphism. Incorporation of lateral substitution with respect to the central core unit led to reductions in transition temperatures; however, the NTB phase was still found to occur. Conversely, utilising branched terminal groups rendered the materials non-mesogenic. Overall, it appears that it is the gross molecular topology that drives the incidence of the NTB phase rather than simple dipolar considerations. Furthermore, dimers lacking any polar groups, which were prepared to test this hypothesis, were found to be non mesogenic, indicating that at the extremes of polarity these effects can dominate over topology.

Relationship between molecular association and re-entrant phenomena in polar calamitic liquid crystals.

The relationship between molecular association and re-entrant phase behavior in polar calamitic liquid crystals has been explored in two families of materials: the 4'-alkoxy-4-cyanobiphenyls (6OCB and 8OCB) and the 4'-alkoxy-4-nitrobiphenyls. Although re-entrant nematic phase behavior has previously been observed in the phase diagram of 6OCB/8OCB, this is not observed in mixtures of the analogous nitro materials. As there is no stabilization of the smectic A phase in mixture studies, it was conjectured that the degree of association for the nitro systems is greater than that for the cyano analogues. This hypothesis was tested by using measured dielectric anisotropies and computed molecular properties to obtain a value of the Kirkwood factor, g, which describes the degree of association of dipoles in a liquid. These computed values of g confirm that the degree of association for nitro materials is greater than that for cyano and offer a useful method for quantifying molecular association in systems exhibiting a re-entrant polymorphism.

The nematic phases of bent-core liquid crystals.

Over the last ten years, the nematic phases of liquid crystals formed from bent-core structures have provoked considerable research because of their remarkable properties. This Minireview summarises some recent measurements of the physical properties of these systems, as well as describing some new data. We concentrate on oxadiazole-based materials as exemplars of this class of nematogens, but also describe some other bent-core systems. The influence of molecular structure on the stability of the nematic phase is described, together with progress in reducing the nematic transition temperatures by modifications to the molecular structure. The physical properties of bent-core nematic materials have proven difficult to study, but patterns are emerging regarding their optical and dielectric properties. Recent breakthroughs in understanding the elastic and flexoelectric behaviour are summarised. Finally, some exemplars of unusual electric field behaviour are described.

Hydrophobic and hydrophilic balance and its effect on mesophase behaviour in hydroxyalkyl ethers of methyl glucopyranoside.

Four series of monosubstituted methyl α-D-glucopyranoside hydroxyalkyl ethers were prepared and their thermotropic and lyotropic self-organising properties were investigated in terms of the hydrophobic-hydrophilic balance with respect to their molecular structures. The results obtained lead us to a new understanding of the forces that drive the formation of condensed soft-matter phases.

Polarised phosphorescent emission in an organoplatinum(II)-based liquid-crystalline polymer.

By combination of mesogenic rod-like cycloplatinated monomers based on 2,5-di(4-alkenyloxyphenyl)pyridine ligands with 1,1,3,3,5,5-tetramethyltrisiloxane, a phosphorescent, liquid-crystalline polymer was obtained, which showed polarised emission.

Supermolecular chiral mesogenic tripedes.

A novel series of chiral liquid crystalline tripedes Glucoside and Mannoside derivatives G(n) and M(n) (n=1-3) have been synthesised. The inner cores consist of methyl α-D-Glucoside G or methyl α-D-Mannoside M, regioselectively functionalised at the less hindered position C6, with tert-butyldimethylsilyl (TBDMS), hydroxyl or carboxylic acid moieties. The cores, which can acquire several flexible conformations, are attached to rod-like smectogenic-preferring cyanobiphenyl units, by means of a flexible hexanoyl spacer. These Glyco-Supermolecules exhibit chiral nematic (N*) and smectic A (SmA) phases. The combined effects of core chirality and functional groups on thermal and mesomorphic characteristics are discussed.

Liquid-crystalline aromatic-aliphatic copolyester bioresorbable polymers.

The synthesis and characterisation of a series of liquid-crystalline aromatic-aliphatic copolyesters are presented. Differential scanning calorimetry showed these polymers have a glass transition temperature in the range 72 degrees C-116 degrees C. Polarised optical microscopy showed each polymer exhibits a nematic mesophase on heating to the molten state at temperatures below 165 degrees C. Melt processing is demonstrated by the production of injection moulded and compression moulded specimens with Young's modulus of 5.7 +/- 0.3 GPa and 2.3 +/- 0.3 GPa, respectively. Wide-angle X-ray scattering data showed molecular orientation is responsible for the increase of mechanical properties along the injection direction. Degradation studies in the temperature range 37 degrees C-80 degrees C are presented for one polymer of this series and a kinetic constant of 0.002 days(-1) is obtained at 37 degrees C assuming a first order reaction. The activation energy (83.4 kJ mol(-1)) is obtained following the Arrhenius analysis of degradation, showing degradation of this material is less temperature sensitive compared with other commercially available biodegradable polyesters. In vitro and in vivo biocompatibility data are presented and it is shown the unique combination of degradative, mechanical and biological properties of these polymers may represent in the future an alternative for medical device manufacturers.