Ionic thermotropic liquid crystal dendrimers

The synthesis and characterization of two families of ionic liquid crystal dendrimers consisting of the ammonium salts of the commercially available poly(amidoamine) (G = 0-5) and poly(propylene imine) (G = 1-5) dendrimers and three long-chain carboxylic acids are reported. The liquid crystalline behavior was investigated by means of differential scanning calorimetry, polarizing light optical microscopy, and X-ray diffractometry. The thermal stability of the ionic materials was further studied by NMR. Most of the dendrimers show lamellar mesomorphism, and two of them exhibit columnar mesomorphism. On the basis of the experimental results, we propose models both at the molecular level and in the mesophase for all the materials.     

Chloromethylsilane functionalised dendrimers: synthesis and reactivity

Tetraallylsilane was functionalised using (chloromethyl)dimethylsilane to give the first generation chloromethyl terminated dendrimer 1. The resulting dendrimer was successfully reacted with K[CpM(CO)₂] (Cp=η⁵-C₅H₅; M=Fe, Ru) to give Si[(CH₂)₃SiMe₂CH₂MCp(CO)₂]₄ functionalised dendrimers in satisfactory yield. Reaction of dendrimer 1 with NaI in acetone gave the -SiMe₂CH₂I functionalised dendrimer, while reactions of 1 with K[CpM(CO)₃] (M=Mo, W, Re), Li[C₅Me₄H], Na[C₅Me₄H], the cobaloxime nucleophile or tert-BuLi were not successful.     

Supermolecular liquid crystal dendrimers based on the octasilsesquioxane core

Liquid crystalline dendrimers are proving to be a fascinating class of materials that possess unusual physical properties. The self-assembling process involved in the formation of the mesomorphic state apparently deforms the spherical disposition of the supermolecular dendrimers to give rod-like entities that pack together to yield disordered Smectic A and smectic C mesophases.     

Supermolecular liquid crystal dendrimers based on the octasilsesquioxane core

Liquid crystalline dendrimers are proving to be a fascinating class of materials that possess unusual physical properties. The self-assembling process involved in the formation of the mesomorphic state apparently deforms the spherical disposition of the supermolecular dendrimers to give rod-like entities that pack together to yield disordered Smectic A and smectic C mesophases.     

X-ray diffraction study of smectic A layering in terminally fluorinated liquid crystal materials

We report an X-ray study of smectic A layering for mesogenic compounds with fluorinated substituents in terminal positions. The measurements were carried out using diffractometers with one- and two-coordinate proportional chambers. It was found that in contrast to -CN or -NO₂ terminated smectics, the polar -OCF₃ compounds form only a monolayer smectic A₁ phase. The ratio of the intensity of the second harmonic to the first in smectic A phases formed by molecules with lengthy perfluorinated chains was found to be two orders of magnitude higher than is commonly reported for low molar mass thermotropic mesogens, indicating deviations of the density distribution function p(z) from a pure sinusoidal form. The layer periodicity d for these mesogens exceeds the molecular length L: d/L ≃ 1·1, which corresponds to a smectic A_d phase consisting of parallel or antiparallel dimers. We have observed that lateral fluorine substitution in the benzene ring adjacent to the perfluorinated chain leads to the disturbance of uniform smectic A layering and to the formation of a defect-modulated smectic A structure of a chequer-board type. For polyphilic compounds containing both hydrogenous and perfluorinated units in the terminal chain, the in-plane structure factor displays double-peaked liquid-like profiles indicating the existence of nearest-neighbour molecular stacking at different distances. The peculiarities of smectic A layering in fluorinated mesogens are discussed in terms of steric coupling and enhanced conformational rigidity of fluorine containing moieties.     

Synthesis and liquid crystal properties of new cyclic carbonate monomers functionalised with cholesteryl moiety

ABSTRACT

Four new liquid crystal cyclic carbonate monomers M₁–M₄, with cholesteryl moiety and flexible spacer of different lengths, were synthesised through coupling reaction. The chemical structures, mesophase properties and thermal behaviour of the monomers were characterised with Fourier transform infrared spectroscopy, proton nuclear magnetic resonance spectroscopy (¹H NMR), polarising optical microscopy, differential scanning calorimetry and X-ray diffraction. Based on these results, the relationship between the number of methylene groups into flexible chain and the mesomorphism of the monomers was investigated. It was found that all the monomers showed a focal conic texture of a smectic A phase and exhibited an interdigitated molecular arrangement. Moreover, the glass transition temperature and the isotropisation temperature of the monomers except M₁ decreased, and the mesophase range narrowed as the number of methylene units into the flexible chain increased.     

Highly congested liquid crystal structures: dendrimers, dendrons, dendronized and hyperbranched polymers

In this tutorial review we describe some studies concerning liquid crystal dendritic polymers. We have chosen to present several representative examples that illustrate the diverse kinds of LC dendritic structures, namely: dendrimers, dendrons, dendronized polymers and hyperbranched polymers. We review their synthesis, mesogenic properties and the way that they are arranged to form supramolecular liquid crystal assemblies.     

Dendromesogens: liquid crystal organizations of poly(amidoamine) dendrimers versus starburst structures

A new series of liquid crystalline poly(amidoamine) (PAMAM) dendrimers is described. These dendrimers are made by attaching to the 0-, 1-, 2-, 3-, and 4-generation of PAMAM-terminal promesogenic units that carry two decyloxy chains in the 3- and 4-positions of their peripheral aromatic ring. X-ray diffraction studies show that all the compounds display a hexagonal columnar mesophase. A high density of aliphatic chains imposes a curved interface with the promesogenic units that forces the molecules to adopt a radial conformation, and therefore, the columnar structure. A model for the supramolecular organization of the different generations within the columnar mesophase is proposed based on the variation of some of the structural parameters.     

Effect of functionalised silver nanoparticle on the elastic constants and ionic transport of a nematic liquid crystal

ABSTRACT

Addition of nanomaterial into pure nematic liquid crystals (NLCs) leads to improvement in the various physical properties of the liquid crystal (LC) host. Doping of nanomaterials affects the local molecular arrangement of the LC molecules. Here, we present the results of our investigation on the effect of functionalised silver nanoparticles (f-AgNPs) on the physical properties of the rod-shaped NLC, 4-trans-pentyl-cyclohexyl cyanobenzene (5PCH). The dielectric constant, threshold voltage, elastic constants, birefringence and conductivity measurements were performed on pure 5PCH and its f-AgNPs doped nanocomposites as a function of temperature in planar cell. The magnitude of dielectric anisotropy, elastic constants and birefringence in nanocomposites were enhanced with increasing concentration of f-AgNPs indicating enhancement of order parameter in the nematic medium. Threshold voltage decreases with increasing concentration of f-AgNPs. Both parallel and perpendicular components of conductivity decrease with increasing concentration of f-AgNPs due to the absorption of ion by the doped f-AgNPs. This observed decrease in conductivity in nanocomposites is further confirmed by calculating the ion transportation number and time of flight. The ion transport number i.e ionic contribution present in the LC cell was found to be 0.966 in pure 5PCH, whereas 0.830 in 0.5 wt% of f-AgNPs nanocomposite of 5PCH.     

Synthesis of terminally substituted stilbene-tolane liquid crystals

Methods for synthesizing substituted alkyl and fluoro stilbene-tolane (PTPDP) liquid crystal materials are presented. These compounds show a slightly higher birefringence than the analogous bistolanes, but higher melting points and heats of fusion. Potential applications of these compounds for optical communications and displays are discussed.     

Synthesis of terminally substituted stilbene-tolane liquid crystals

Methods for synthesizing substituted alkyl and fluoro stilbene-tolane (PTPDP) liquid crystal materials are presented. These compounds show a slightly higher birefringence than the analogous bistolanes, but higher melting points and heats of fusion. Potential applications of these compounds for optical communications and displays are discussed.     

Nanohybrids from liquid crystalline extended amphiphilic dendrimers

A novel extended amphiphilic dendrimer with linear poly(ethylene oxide) (PEO) attached to a PEO-like dendritic core as hydrophilic fraction and eight docosyl chain branches as hydrophobic fraction has been prepared for the use as structure-directing agent for silica-type materials. The extended dendrimer exhibits a hexagonal columnar liquid crystalline phase in the melt. Organically modified inorganic precursors and the extended dendrimer co-assemble into nanostructured hybrids. Hybrids with 0.44 weight fraction (fw) of aluminosilicate show a lamellar morphology, while hybrids with 0.21 fw exhibit a cylindrical structure. Nanostructures were characterized by a combination of small-angle X-ray scattering (SAXS), transmission electron microscopy (TEM), and atomic force microscopy (AFM). The results suggest that dendrimer-based amphiphiles may provide an exciting platform for the formation of multifunctional organic-inorganic nanostructured hybrid materials with unique structural characteristics.     

A strongly positive dendrimer effect in asymmetric catalysis: allylic aminations with Pyrphos-palladium functionalised PPI and PAMAM dendrimers

A remarkable and unprecedented increase in catalyst selectivity in dendrimer catalysis is observed for the Pyrphos-Pd catalysed allylic amination of 1,3-diphenyl-1-acetoxypropene as a function of the dendrimer generation (with up to 64 metal sites). This steady increase in ee-values for the allylic amination is less pronounced for the poly(propyleneimine)-derived catalysts than for the corresponding palladium-PAMAM dendrimer catalysts for which an increase in selectivity from 9% ee for a mononuclear reference system to 69% ee for the Pd64-dendrimer was found.     

Low-birefringence liquid crystal mixtures for photonic liquid crystal fibres application

ABSTRACT

Series of low-birefringence liquid crystal mixtures composed of alkyl alkylbicyclohexyl carbonates and modified mixtures with other compounds have been formulated, their refractive indices and electric permittivity measured upon temperature. They exhibit the ordinary refraction index n_o lower than the refractive index of silica glass in a different range of temperature. This enables to observe in photonic liquid crystal fibres (PLCFs) a change in the light propagation mechanism from photonic band gap guiding to modified total internal reflection at different temperatures. Selected applications of PLCFs are also discussed.     

The relationship between liquid crystal alignment in the nematic and smectic C* phases

The pretilt angle in the nematic phase is related to two different surface dependent factors, while the quality of surface stabilized ferroelectric liquid crystal (SSFLC) devices is dependent on only one of them. We have synthesized two series of polyalkyleneimides and found that the pretilt angles for thick nematic cells are not related to the cone angles in SSFLC cells.     

Polydispersity in liquid crystal systems

Here we discuss the statistical mechanics of polydisperse liquid crystal systems. Three different kinds of liquid crystal systems are treated: nematic order in thermotropic Maier-Saupe-like systems and in lyotropic Onsager-like rod systems, and smectic order in a perfectly aligned hard rod fluid. In the first two cases we calculate the broadening of the isotropic-nematic transition. In the last case the suppression of smectic order is dealt with. We discuss the relationship between real systems and the models discussed in the paper.     

Memory effects in chiral nematic liquid crystals doped with functionalised single-walled carbon nanotubes

Octadecylamine-functionalised single-walled carbon nanotubes (SWCNTs) were dispersed into nematic liquid crystals (LCs) doped with chiral molecules. The collective orientation of nematic LC molecules in helical layers was manipulated by varying dopant concentration. Highly anisotropic nature of SWCNTs enhanced the anisotropy of the LC as confirmed by polarised fluorescence spectroscopy. The π–π interaction of SWCNTs present in the planar alignment layers and twisted nematic LC molecules affects the molecular relaxation process. An irreversible electro-optic memory in the material has been observed.     

Fluorescence behaviour of cyanobiphenyl liquid crystal molecules in liquid crystal/polymer composite films

The fluorescence behaviour of the liquid crystal, 4-cyano-4-pentylbiphenyl (5CB), in composite thin films prepared by the photopolymerization of 5CB/diacrylate mixtures, was investigated by means of three different excitation methods, in which the total-internal-reflection or surface-limited excitation method was used for analysis of the fluorescence from an ultra-thin interface layer ( 100nm) in contact with the substrate surface, whereas the fluorescence from the interior bulk was analysed by the through-film excitation method. It was found that intensity ratios of the monomer and excimer emissions of 5CB are significantly lower in the interface layer than in the interior bulk, depending upon photopolymerization conditions as well as upon the structures of the diacrylates used. Scanning electron microscopic observations and light-scattering measurements of some typical composite films showed possible relationships between morphological features and fluorescence characteristics depending upon the diacrylate structures and polymerization conditions. The different fluorescence behaviour has been discussed in terms of differences in mobility and/or aggregation degrees of 5CB molecules arising from dominant molecular interactions with the substrate and polymer surfaces.     

Control of liquid crystal droplet configuration in polymer dispersed liquid crystal with macro-iniferter polystyrene

A polystyrene macro-iniferter was applied to control the alignment of liquid crystal molecules at the droplet wall of polymer dispersed liquid crystal (PDLC) films. The aspects of the alignment were monitored by observing the droplet in the PDLC film. With increasing the macro-iniferter polystyrene in the composition, the configuration of LC droplets changes from bipolar to radial. This is because the high concentration of the macro-iniferter polystyrene results in a small surface interaction between the LC and the polymer matrix, which favours the formation of radial configuration. The radial configuration was stable under our conditions. However, increasing the LC and the initiator concentrations resulted in the change from radial to bipolar.     

Robust liquid crystal droplets

The preparation and properties of cyanobiphenyl liquid crystal droplets encapsulated by the polymerizable lecithin 1,2-bis(10,12-tricosadiynoyl)-sn-glyero-3-phosphocholine (DC_8,9PC) are described. Under a wide variety of preparation conditions the droplets obtain a diameter of approximately 10 mum. These droplets are stable for periods of over one year at room temperature. Furthermore, they are stable upon temperature cycling between the nematic and isotropic phases and between the smectic A to nematic to isotropic phase transitions.