Cinnamate-functionalized hyperbranched polymer as liquid crystal photo-alignment layer

In this work, 4-methoxylcinnamoyl chloride was reacted with a commercial hyperbranched polymer （Boltom-TM H30） to prepare a hyperbranched photosensitive polymer （H30-Ci）. The polymer was characterized by UV absorption spectrum and 1H- NMR spectrum. After processed by Linearly Polarized Polymerization （LPP） method, the spin-coated films of H30-Ci were used as photo-alignment layers to assemble liquid crystal （LC） cells containing nematic liquid crystal （5CB）. The observation by polarized microscope showed that the H30-Ci blended with a linear polymer （BP-AN-Ci） photo-alignment layers could align LC molecules in a very uniform way.     

The influence of nematic liquid crystal content on the electro-optical properties of a polymer dispersed liquid crystal prepared with monodisperse liquid crystal microcapsules

Highly monodisperse poly(methylmethacrylate) (PMMA)/liquid crystal (LC) microcapsules were prepared by the solute codiffusion method (SCM). In SCM, the solvency of the dispersion medium and the swelling temperature were controlled to ensure complete swelling of the LC into the PMMA substrate particles. After the solvent evaporation procedure, mononuclear LC domains were formed in every particle, and overall the LC microcapsules maintained a spherical shape, monodispersity and smooth surface. PDLC cells prepared using the LC microcapsules exhibited an excellent contrast ratio and transmittance. By increasing the LC content in these LC microcapsules, the electro-optical properties of PDLC cells have been greatly improved.     

Photochemical tuning capability of cholesteric liquid crystal cells containing chiral dopants end capped with menthyl groups

In order to investigate the photochemical tuning capability of chiral monomers and polymers containing end-capped menthyl groups, a new series of chiral dopants was synthesized and added to commercially available nematic liquid crystals to induce cholesteric liquid crystal (LC) phases. The addition of chiral dopants with azo structure led to phototunability of the reflection colour of the LC cells. Photochromic variation of the LC cells due to photoisomerization of the azo compound was investigated. After photopolymerization of the monomers inside the cholesteric LC cells, the centre wavelength of the reflected band of the incident light was found to be fixed and the reflected bandwidth was broadened, resulting in a red shift. A schematic representation of both the photoisomerization of the azo dopants and its effect on variation of twisting pitches is proposed. Real image recording was performed using 365 nm UV through a mask with text. The top and side views of the morphological network structures of a fabricated cholesteric LC cell were investigated using scanning electron microscopy. The results of this investigation demonstrated that RGB reflected colours of LC cells can easily be achieved through the addition of the menthyl-containing synthesized chiral compounds to nematic LCs. The addition of synthesized AzoM helped further in recording the patterns onto cholesteric LC films using 365 nm UV exposure.     

Photochemical tuning capability of cholesteric liquid crystal cells containing chiral dopants end capped with menthyl groups

In order to investigate the photochemical tuning capability of chiral monomers and polymers containing end‐capped menthyl groups, a new series of chiral dopants was synthesized and added to commercially available nematic liquid crystals to induce cholesteric liquid crystal (LC) phases. The addition of chiral dopants with azo structure led to phototunability of the reflection colour of the LC cells. Photochromic variation of the LC cells due to photoisomerization of the azo compound was investigated. After photopolymerization of the monomers inside the cholesteric LC cells, the centre wavelength of the reflected band of the incident light was found to be fixed and the reflected bandwidth was broadened, resulting in a red shift. A schematic representation of both the photoisomerization of the azo dopants and its effect on variation of twisting pitches is proposed. Real image recording was performed using 365 nm UV through a mask with text. The top and side views of the morphological network structures of a fabricated cholesteric LC cell were investigated using scanning electron microscopy. The results of this investigation demonstrated that RGB reflected colours of LC cells can easily be achieved through the addition of the menthyl‐containing synthesized chiral compounds to nematic LCs. The addition of synthesized AzoM helped further in recording the patterns onto cholesteric LC films using 365 nm UV exposure.     

Optical behaviour of photoimageable cholesteric liquid crystal cells with various novel chiral compounds

In theory, both polarity and steric hindrance are basic factors which affect molecular interactions. To investigate the optical properties and steric structures of chiral compounds having different chiral moieties which affect the wavelength of light reflection in liquid crystal (LC) cells, a series of novel chiral compounds and azobenzene derivatives were synthesized. The liquid crystalline phases of the compounds were identified using small angle X‐ray diffraction, differential scanning calorimetry and polarizing optical microscopy. Cholesteric LC cells with various synthesized chiral dopants which selectively reflect visible light were first prepared, the photochemical switching behaviour of colours was then investigated, with special reference to the change in transmittance in cholesteric LC cells containing an azobenzene derivative as a photoisomerizable guest molecule. Reversible isomerization of azobenzene molecules occurred in the cholesteric systems, resulting in a depression of T _ChI and a shift of the selectively reflected wavelength. We discuss the photochemically driven change in the helical pitch of the cholesteric LCs with respect to structural effects involving the chiral moieties. Molecular interactions caused by the added dopants, reliability and stability of the photoisomerization, and UV irradiation effects on the cholesteric LC cells were also investigated. A real image was recorded through a mask on a cholesteric LC cell fabricated in this investigation.     

Optical behaviour of photoimageable cholesteric liquid crystal cells with various novel chiral compounds

In theory, both polarity and steric hindrance are basic factors which affect molecular interactions. To investigate the optical properties and steric structures of chiral compounds having different chiral moieties which affect the wavelength of light reflection in liquid crystal (LC) cells, a series of novel chiral compounds and azobenzene derivatives were synthesized. The liquid crystalline phases of the compounds were identified using small angle X-ray diffraction, differential scanning calorimetry and polarizing optical microscopy. Cholesteric LC cells with various synthesized chiral dopants which selectively reflect visible light were first prepared, the photochemical switching behaviour of colours was then investigated, with special reference to the change in transmittance in cholesteric LC cells containing an azobenzene derivative as a photoisomerizable guest molecule. Reversible isomerization of azobenzene molecules occurred in the cholesteric systems, resulting in a depression of T_ChI and a shift of the selectively reflected wavelength. We discuss the photochemically driven change in the helical pitch of the cholesteric LCs with respect to structural effects involving the chiral moieties. Molecular interactions caused by the added dopants, reliability and stability of the photoisomerization, and UV irradiation effects on the cholesteric LC cells were also investigated. A real image was recorded through a mask on a cholesteric LC cell fabricated in this investigation.     

High-transmittance liquid crystal cell fabricated using nanoparticle-doped polyimide

We found that we can increase the transmittance of a liquid crystal (LC) cell by doping the alignment material with nanoparticles. We fabricated an LC cell using indium–tin–oxide glass substrates coated with SiO₂-doped polyimide. We confirmed that the transmittance of LC cells fabricated using SiO₂-doped polyimide was higher than that of LC cells fabricated using pure polyimide. To account for the increase of transmittance, we measured the order parameter of the fabricated LC cells and investigated the surface morphology of the alignment layer using atomic force microscopy.     

Photo-driven liquid crystal cell with high sensitivity

The photo-driven LC cell was assembled by sandwiching the liquid crystal material between two quartz or ITO plates covered with a 'command layer', which was fabricated from azobenzene-grafted ladder-like polysilsesquioxanes. The improved response sensitivity of the photo-driven cell, which means a lower threshold driving UV light intensity and a faster risetime, was achieved in two ways: pre-rubbing of the command surface and application of an assisting critical in-plane mode electric field. The response behaviour of the photo-driven cell was measured in situ and data were collected by computer. The results show that the risetime (4 s) under a weak UV intensity of 0.5 mWcm -2 is shorter than previously reported (several tens of seconds) under a greater UV intensity of 3-5 mWcm -2. The improved photo-driven LC cell holds out promise of potential applications in photo-addressing and photo-recording.     

Photo-driven liquid crystal cell with high sensitivity

The photo-driven LC cell was assembled by sandwiching the liquid crystal material between two quartz or ITO plates covered with a 'command layer', which was fabricated from azobenzene-grafted ladder-like polysilsesquioxanes. The improved response sensitivity of the photo-driven cell, which means a lower threshold driving UV light intensity and a faster risetime, was achieved in two ways: pre-rubbing of the command surface and application of an assisting critical in-plane mode electric field. The response behaviour of the photo-driven cell was measured in situ and data were collected by computer. The results show that the risetime (4 s) under a weak UV intensity of 0.5 mWcm -2 is shorter than previously reported (several tens of seconds) under a greater UV intensity of 3-5 mWcm -2. The improved photo-driven LC cell holds out promise of potential applications in photo-addressing and photo-recording.     

Network morphology and electro-optical characterisations of epoxy-based polymer stabilised liquid crystals

ABSTRACT

In this paper, by utilising the photoinitiated cationic polymerisation of liquid crystalline epoxide in LC solvents, the epoxy-based polymer stabilised liquid crystals (EPSLCs) were fabricated. The effects of the liquid crystalline epoxide content, UV intensity, polymerisation temperature, and initiator content on the network morphology of liquid crystalline epoxy polymers (LCEPs) and electro-optical characterisations of EPSLC samples were studied. The results suggested that the preparation conditions had a dominant effect on the morphology of the LCEP and the void size in the EPSLC sample. The increase of liquid crystalline epoxide content, UV intensity, and initiator content induced that the density of LCEP network became larger and the void size decreased, which resulted in that the stabilising effect from the LCEP network on the mesogenic solvent molecules was strengthened. Conversely, the increase of polymerisation temperature induced that the stabilising effect from the LCEP network on the LC molecules was weakened.     

Bent-core liquid crystal-functionalised flexible polymer substrates for liquid crystal alignment

ABSTRACT

A transparent flexible polymer film is chemically functionalised with a bent-core liquid crystal (BCLC) compound for effective alignment of the bulk BCLC sample at the substrate–LC interface. The surface attachment was achieved via a simple procedure which involved pre-treatment of the polymer film (commercial name: over head projector film) using piranha solution followed by chemically attaching the BCLC compound through silane condensation reaction. Surface characterisation of the unmodified and BC-modified flexible films was carried out through X-ray photoelectron spectroscopy (XPS), attenuated total reflectance fourier transform infrared (ATR-FTIR) spectroscopy, contact angle (CA) and atomic force microscopy (AFM) techniques. The BC-modified flexible substrates are analysed for their efficiency to orient the bulk LC sample. Remarkably, the chemically modified polymer substrates are highly efficient in vertically aligning both the BC and rod-like LC samples at the substrate–LC interface, in comparison to their unmodified counterparts. The described method is simple, reproducible, surface modified substrates are highly stable and more importantly reusable. The demonstrated method for the alignment of BCLCs advances a step forward towards the realisation of applications proposed for these fascinating compounds.     

Small dosage of holographic exposure via a He-Ne laser to fabricate tunable liquid crystal phase gratings operated with low electric voltages

The fabrication processes of tunable liquid crystal (LC) phase gratings via small dosage of holographic exposure of a He-Ne laser beam were investigated. The initial LC cells were filled with various ratios of ingredients mainly including LCs and photocurable monomers. The fabricated LC phase gratings shown in the Raman–Nath regime possessed a maximum value of first-order diffraction efficiency close to 33.3% at 5.8 V_rms. Furthermore, optimised grating was demonstrated and used as an interference recorder in holography.     

Vertical alignment of liquid crystal on tocopherol-substituted polystyrene films

We synthesised a series of vitamin-based and renewable tocopherol-substituted polystyrene (PTOC#, # = 20, 40, 60, 80 and 100), where # is the molar content of tocopherol moiety, using polymer analogous reactions to investigate their liquid crystal (LC) alignment properties. In general, the LC cell fabricated using the polymer film having a higher molar content of tocopherol side group showed vertical LC alignment behaviour. The vertical alignment (VA) behaviour was well correlated with the surface energy value of these polymer films. For example, VA was observed when the surface energy values of the polymer were smaller than about 35.22 mJ/m² generated by the nonpolar tocopherol moiety having long and bulky carbon groups. Good electro-optical characteristics, such as voltage holding ratio and residual DC voltage, and aligning stabilities at 200°C and ultraviolet irradiation of 10 J/cm² were observed for the LC cells fabricated using PTOC100 as a LC alignment layer. Therefore, it was first found that the renewable tocopherol-based materials can produce an eco-friendly vertical LC alignment system.     

Effect of chemical structures of polyimides on photosensitivity of liquid crystal alignment using a polarized UV exposure

Unidirectional liquid crystal (LC) alignment produced by polarized UV exposure was examined using polyimides (PIs) synthesized using different diamines. The dichroic ratio of the resulting LC cells suggests that the UV photosensitivity is primarily controlled by the chemical structures of the PIs used. The UV absorption and fluorescence spectra of the PI films, and molecular conformations of the diamines, indicate that the photosensitivity is controlled by the UV absorption efficiencies and molecular conformations of the PIs.     

Fabrication of photoluminescent liquid crystal device using an in situ self-assembled molecular layer of a pyrene derivative

An in situ self-assembled molecular layer of 1-pyrenesulfonic acid sodium salt as an alignment agent was formed on indium tin oxide substrates for vertically aligning liquid crystals (LCs). The thus-aligned LCs exhibited uniform vertical alignment under crossed polarisers. The electro-optical characteristic of the LC cell fabricated using this method exhibited better performance than those of conventional LC cells with a polyimide alignment layer. Because the proposed alignment method is a simple one and involves low concentrations of the alignment agent (0.05 wt%), it is highly cost-effective. Further, the pyrene derivative, when mixed with LCs, exhibited photoluminescence (PL) under ultraviolet light. Given that the proposed method resulted in highly vertically aligned LCs and the alignment agent exhibited PL, the method should find wide use in the fabrication of colour-filter-free LC displays.     

Fabrication of coloured liquid crystal device using photoluminescent biomolecular chlorophyll

We fabricated a coloured liquid crystal (LC) device using photoluminescent biomolecular chlorophyll. The chlorophyll molecule, which is inexpensive because of its abundance in nature, was doped in the LCs for manufacturing the coloured LC device. We confirmed the green colour property of the LC doped with chlorophyll dye using UV-vis spectroscopy. Although the LC cell filled with 0.5 wt% chlorophyll showed good vertical alignment and fast response time, the doping of LC medium with 1.5 wt% chlorophyll resulted in imperfect vertical alignment and slowed response time due to the aggregation of chlorophyll molecules at high concentration. Furthermore, the photoluminescence (PL) characteristics of the LC doped with chlorophyll were investigated using PL spectroscopy. The coloured LC cell doped with chlorophyll dye showed emission in the red wave number region under UV light. As the LC doped with chlorophyll exhibited good colour performance, conventional colour filter layers could be avoided with the employment of the proposed coloured LC device. By controlling the light source, it is possible to apply the advanced LC device for colour switching. Moreover, a full-colour-switching LC device can be realised using various biomolecular dyes that can emit other colours.     

The effect of mono-sized liquid crystal domains on electro-optical properties in a polymer dispersed liquid crystal prepared by using monodisperse poly(methylmethacrylate)/liquid crystal microcapsules

Highly mono-sized poly(methyl methacrylate) (PMMA)/liquid crystal (LC) microcapsules having a mono-sized single LC domain were prepared by the solute codiffusion method and solvent evaporation. The size of the LC domain in the microcapsules could be controlled by the amount of LC introduced during the swelling stage. The electro-optical properties of the polymer dispersed liquid crystal (PDLC) prepared by using the microcapsules was highly improved. In particular, the threshold voltage was lowered and the switching behaviour with an applied electric field was sharpened drastically compared with PDLC prepared simply by solvent evaporation-induced phase separation.     

The effect of mono-sized liquid crystal domains on electro-optical properties in a polymer dispersed liquid crystal prepared by using monodisperse poly(methylmethacrylate)/liquid crystal microcapsules

Highly mono-sized poly(methyl methacrylate) (PMMA)/liquid crystal (LC) microcapsules having a mono-sized single LC domain were prepared by the solute codiffusion method and solvent evaporation. The size of the LC domain in the microcapsules could be controlled by the amount of LC introduced during the swelling stage. The electro-optical properties of the polymer dispersed liquid crystal (PDLC) prepared by using the microcapsules was highly improved. In particular, the threshold voltage was lowered and the switching behaviour with an applied electric field was sharpened drastically compared with PDLC prepared simply by solvent evaporation-induced phase separation.     

Determination of flurbiprofen in pharmaceutical formulations by UV spectrophotometry and liquid chromatography

In this study, a new and rapid UV spectrophotometric (UV) method and a reversed phase high performance liquid chromatographic (LC) method were developed for quantitative estimation of flurbiprofen, a non-selective, non-steroidal, anti-inflammatory drug (NSAID), in pure form and in pharmaceutical dosage form. The solvent system, wavelength of detection, chromatographic conditions were optimized in order to maximize the sensitivity of both the proposed methods. The linear regression equations obtained by least square regression method were Abs=7.5906×10⁻² concentration (μg/ml) + (−) 4.6210×10⁻² for the UV method, and peak area=1.2652×10² concentration (ng/ml) + 1.4830×10³ for the LC method. The detection limit as per the error propagation theory was found to be 0.34 μg/ml for UV method and 15 ng/ml for LC method. The developed methods were successfully employed with high degree of precision and accuracy for the estimation of total drug content in two commercial ophthalmic drops of flurbiprofen. The results of analysis were treated statistically, as per USP 2000 and International Conference on Harmonization (ICH) guidelines for validation of analytical procedures, and by recovery studies. The results obtained from UV method were comparable with those obtained by using LC. It was concluded that both the developed methods are equally accurate, sensitive, precise, reproducible, robust and rugged and could be applied directly and easily to the pharmaceutical preparations of flurbiprofen. However, LC method is useful at very low level (ng/ml), whereas UV method is suitable at μg/ml level.