Effect of alkyl chain length in the terminal ester group on mesomorphic properties of new chiral lactic acid derivatives

Two series of new liquid crystalline lactic acid derivatives with a terminal ester group have been synthesised. The effect of this ester unit and the length of its alkyl chain on the mesomorphic and dielectric properties of the compounds exhibiting a broad temperature range of chiral smectic phases have been studied. We found that the mesomorphic behaviour and phase transition temperatures are strongly affected by the molecular architecture. Depending on the alkyl chain length in the terminal ester unit, the studied materials exhibited paraelectric smectic A*, ferroelectric tilted smectic C* and antiferroelectric smectic C_A* phases over a broad temperature range. The physical properties of the compounds have been studied by optical polarising microscopy, differential scanning calorimetry, electro-optic measurements, small-angle X-ray scattering and dielectric spectroscopy. Furthermore, the homologues with short terminal alkyl chains showed a very small layer shrinkage at the transition from the orthogonal SmA* to the tilted SmC* phase, which is a characteristic feature of ‘de Vries-type’ behaviour.     

Several types of bilayer smectic liquid crystals with ferroelectric and antiferroelectric properties in binary mixture of dimeric compounds

The mesomorphic behavior and phase structure were examined in the mixture of two kinds of dimeric compounds, alpha,omega-bis(4-alkoxyanilinebenzylidene-4'-carbonyloxy)pentane (mOAM5AMOm), by optical microscopy, X-ray diffraction, polarization switching, and second-harmonic generation measurements. One compound is 4OAM5AMO4 with a short terminal alkyl chain that forms a single-layer smectic phase (SmCAs) with a random mixing of spacer and tail groups. Another compound is 16OAM5AMO16 with a long terminal alkyl chain that forms a chiral, anticlinic, and antiferroelectric bilayer phase (SmCAb) with the bent molecules tilted to the bilayer. By mixing these two compounds, the SmCAs phase of 4OAM5AMO4 is easily destabilized, leading to the wide content region of the bilayer phases. In the bilayer regime, three other smectic phases are newly induced. Two of them are antiferroelectric and ferroelectric phases in which the molecules lie perpendicularly with respect to the layer. The other shows no polar response to an external electric field and behaves like a smectic A. The new appearance of these bilayer phases is discussed as a mixing effect of long and short tail groups.     

Direct transition from the SmA phase to the tilted hexatic phase in liquid crystals with several lactate units

Compounds with differing numbers of lactate units in the chiral part were synthesized. For all materials, at least two smectic phases were found. In addition to the SmA, the SmC* and/or the tilted hexatic SmI*(F*) phase appear according to the length of the non-chiral alkyl chain. For the shortest non-chiral chain, a direct transition from the SmA phase to the SmI*(F*) phase has been discovered and studied. For compounds with the 2-(S)-methylbutyl alkyl chain and two lactate units in the chiral part the antiferroelectric SmC*_A phase occurs. The ferroelectric character of the hexatic phase has been confirmed even just below the SmC*_A phase.     

Direct transition from the SmA phase to the tilted hexatic phase in liquid crystals with several lactate units

Compounds with differing numbers of lactate units in the chiral part were synthesized. For all materials, at least two smectic phases were found. In addition to the SmA, the SmC* and/or the tilted hexatic SmI*(F*) phase appear according to the length of the non-chiral alkyl chain. For the shortest non-chiral chain, a direct transition from the SmA phase to the SmI*(F*) phase has been discovered and studied. For compounds with the 2-(S)-methylbutyl alkyl chain and two lactate units in the chiral part the antiferroelectric SmC*_A phase occurs. The ferroelectric character of the hexatic phase has been confirmed even just below the SmC*_A phase.     

Achiral bent-core azo compounds: observation of photoinduced effects in an antiferroelectric tilted smectic mesophase

We report the synthesis and physical properties of four novel bent-core compounds, containing an azo linkage and alkyl terminal chains. It is found that, except for the lowest homologue, all the materials are liquid crystalline, exhibiting columnar or tilted polar smectic phases. In one of the compounds a reversible photoinduced variation of the spontaneous polarization of the antiferroelectric state was observed.     

Achiral bent-core azo compounds: observation of photoinduced effects in an antiferroelectric tilted smectic mesophase

We report the synthesis and physical properties of four novel bent-core compounds, containing an azo linkage and alkyl terminal chains. It is found that, except for the lowest homologue, all the materials are liquid crystalline, exhibiting columnar or tilted polar smectic phases. In one of the compounds a reversible photoinduced variation of the spontaneous polarization of the antiferroelectric state was observed.     

Banana‐shaped mesogens: mesomorphic properties of seven‐ring esters derived from 5‐chlororesorcinol

Two new homologous series of seven‐ring bent‐core compounds derived from 5‐chlororesorcinol have been synthesized. Many of the lower homologues in both series exhibit the rectangular columnar B₁ phase. However, the three analogous compounds having long terminal alkyl chains exhibit a switchable lamellar phase, which is different from the usual B₂ phase. Although the ground state structure of the mesophase is antiferroelectric, it shows chiral conglomerates with opposite tilt and polarity. Simultaneously, racemic structures are also seen. The mesophases have been characterized using a combination of polarized light microscopy, X‐ray diffraction and electro‐optical studies.     

Helix parameters in bi- and multicomponent mixtures composed of orthoconic antiferroelectric liquid crystals with three ring molecular core

Eight types of bicomponent systems composed of antiferroelectric compounds with different polarity of achiral chain and different temperature dependence of helical pitch as well as three multicomponent mixtures composed of antiferroelectric compounds with opposite helical twist sense were studied. The phase miscibility was tested by polarising optical microscopy. The results of the helical pitch and helical twist sense measurements obtained by a spectrophotometric method of selectively reflected light and by polarimetric method, respectively, are presented. It was found that it is possible to control helical pitch length and temperature of helix twist inversion in antiferroelectric mixtures by controlling the ratio of compounds with left- and right-handed helix in such mixtures, although all of them have the same chiral terminal chain.     

Study on the molecular orientation of an anti-ferroelectric liquid crystal by two-dimensional correlation polarized infrared spectroscopy

Polarization-dependent infrared spectra of an antiferroelectric liquid crystal in the phase were measured at 60°C, for investigation of the relative orientation of the terminal alkyl chain and mesogen. The polarization angle-dependent infrared spectra obtained were analysed by two-dimensional (2D) correlation spectroscopy. The orientation of the mesogen segment and the alkyl chains in the phase is similar to that in the SmC* phase. Four new CH₃ and CH₂ stretching modes were observed from the 2D correlation spectra. From these we can clearly separate the vibrational mode for two hydrocarbon chains and conclude that the orientations of the two chains are different. The C=O group adjacent to the chiral segment is also separated by 2D correlation spectra into two bands, which may arise from either the C=O group hydrogen-bonded with the phenyl ring, or from another rotational conformation of the molecule.     

Effect of introducing thioether linkages on the molecular organization of chiral twin liquid crystals

Novel symmetric and non-symmetric chiral twin compounds possessing one or two thioether groups in a central spacer were prepared, and the effect of substituting oxygen for sulphur on the liquid crystalline properties investigated. Chiral twin compounds possessing an alkylsulphanyl spacer showed an antiferroelectric phase exclusively. However, replacing the alkyloxy chain of the analogous monomer by the alkylsulphanyl chain has no significant effect on the phase transition behaviour, i.e. both of the monomers showed the ferro- and ferri-electric phases as well as the antiferroelectric phase. Thus, different effects of introducing the thioether linkage were for the first time observed between twin and monomeric systems. The introduction of oxygen or sulphur atoms into the central alkyl spacer of the chiral twin was also investigated, and these modifications were found to stabilize the SmA phase. Furthermore, the twin compound possessing a thiaalkyl spacer showed two different molecular assemblies in the smectic A phase.     

Effect of introducing thioether linkages on the molecular organization of chiral twin liquid crystals

Novel symmetric and non-symmetric chiral twin compounds possessing one or two thioether groups in a central spacer were prepared, and the effect of substituting oxygen for sulphur on the liquid crystalline properties investigated. Chiral twin compounds possessing an alkylsulphanyl spacer showed an antiferroelectric phase exclusively. However, replacing the alkyloxy chain of the analogous monomer by the alkylsulphanyl chain has no significant effect on the phase transition behaviour, i.e. both of the monomers showed the ferro- and ferri-electric phases as well as the antiferroelectric phase. Thus, different effects of introducing the thioether linkage were for the first time observed between twin and monomeric systems. The introduction of oxygen or sulphur atoms into the central alkyl spacer of the chiral twin was also investigated, and these modifications were found to stabilize the SmA phase. Furthermore, the twin compound possessing a thiaalkyl spacer showed two different molecular assemblies in the smectic A phase.     

The effect of the alkyl chain length on the mesomorphic properties of new lactic acid derivatives

New series of lactic acid derivatives with alkyl terminal chain have been synthesised and their mesomorphic properties studied. We have varied the length of chiral and non-chiral terminal alkyl chains and found that prolonging both chains has a strong effect on the SmA*–SmC* phase transition. Most of the new materials exhibit only paraelectric SmA* phase; for homologues with a longer non-chiral chain (m ≥ 10), the ferroelectric (SmC*) phase appears below the SmA* on cooling and persists down to a room temperature. The role of the chiral terminal chain in the molecule is quite opposite – only its short length supports the existence of ferroelectric phase. Additionally, a hexatic phase appeared below the SmA*–SmC* phase sequence for several homologues at low temperatures. All materials have been studied using standard experimental techniques (differential scanning calorimetry (DSC), texture observations, polarisation and tilt angle measurements, etc.). Liquid crystalline properties of new materials have been compared with the previously prepared and studied lactic acid derivatives.     

The influence of structure and concentration of cyano-terminated and terphenyl dopants on helical pitch and helical twist sense in orthoconic antiferroelectric mixtures

A bicomponent mixture in the orthoconic aniferroelectric phase, based on three-ring esters with fluorine atoms and ether group in a nonchiral chain, was doped with a variety of cyano-terminated compounds containing different numbers of phenyl rings in a rigid core and a terminal chain of different chirality. Compounds with two chiral chains were added to the basic mixture. The influence of the structure and concentration of dopant on the temperature-dependence of helical parameters, such as helical pitch and twist sense, were assessed by spectrophotometric and polarimetric methods. Long cyano-terminated compounds were found to be better than the other dopants tested for improving the usable properties of the antiferroelectric mixtures.     

Polar Order,Mirror Symmetry Breaking,and Photoswitching of Chirality and Polarity in Functional Bent-Core Mesogens

In recent years, liquid crystals (LCs) responding to light or electrical fields have gained significant importance as multifunctional materials. Herein, two new series of photoswitchable bent-core liquid crystals (BCLCs) derived from 4-cyanoresorcinol as the central core connected to an azobenzene based wing and a phenyl benzoate wing are reported. The self-assembly of these molecules was characterized by differential scanning calorimetry (DSC), polarizing light microscopy (POM), electro-optical, dielectric, second harmonic generation (SHG) studies, and XRD. Depending on the direction of the COO group in the phenyl benzoate wing, core-fluorination, temperature, and the terminal alkyl chain length, cybotactic nematic and lamellar (smectic) LC phases were observed. The coherence length of the ferroelectric fluctuations increases continuously with decreasing temperature and adopts antipolar correlation upon the condensation into superparaelectric states of the paraelectric smectic phases. Finally, long-range polar order develops at distinct phase transitions; first leading to polarization modulated and then to nonmodulated antiferroelectric smectic phases. Conglomerates of chiral domains were observed in the high permittivity ranges of the synclinic tilted paraelectric smectic phases of these achiral molecules, indicating mirror symmetry breaking. Fine-tuning of the molecular structure leads to photoresponsive bent-core (BC)LCs exhibiting a fast and reversible photoinduced change of the mode of the switching between ferroelectric- and antiferroelectric-like as well as a light-induced switching between an achiral and a spontaneous mirror-symmetry-broken LC phase.     

Antiferroelectric phase induced by a semi-fluoroalkane positioned at the chiral tail of a molecule

A novel fluorinated chiral liquid crystal material derived from a newly designed optically active semi-perfluorinated alkyl chain in the chiral group, (S)-1-(2,2,3,3,3-pentafluoropropyloxy)-2-propanol, and a non-fluorinated homologue derived from (S)-1-propyloxy-2-propanol, were prepared for comparison of their mesomorphic properties. The investigation of defect textures, switching behaviour and dielectric permmitivity showed that the introduction of a semi-perfluorinated alkyl chain into the chiral tail of the molecule induces formation of an antiferroelectric phase.     

Ferroelectric compounds with chiral (S)-1-methylheptyloxycarbonyl terminal chain – their miscibility and a helical pitch

Compounds with the same chiral terminal chain but different structure of rigid core and non-chiral terminal chain were added to basic highly tilted ferroelectric compound in the aim of establishing whether the miscibility of phases, especially ferroelectric phase, exists in these compounds and what are the helical pitch and tilt angle temperature dependence in bicomponent systems. In certain systems, we obtained a mixture with very short helical pitch at broad temperature range of ferroelectric phase, which open opportunities for the formulation of multicomponent mixtures for fast switching ferroelectric liquid crystals modes.     

Liquid crystalline dimers with bent-core mesogenic units

Two series of dimers, in which two identical aromatic bent core mesogenic units are connected via an organosiloxane or an alkylene spacer, have been investigated. The dimers with a spacer consisting of a trisiloxane central group and relatively long alkylene groups show an intercalated tilted smectic structure. The layer spacings appear to be very weakly dependent on the terminal chain lengths. In these dimers the smectic phase is stabilized for the compounds with a short terminal chain. Dimers with an aliphatic alkylene spacer are liquid crystalline only when the spacer is relatively short and the terminal chains are long. For these dimers a monolayer tilted smectic phase is observed.     

An homologous series of 6-O-n-alkyl-alpha-D-galactopyranoses: synthesis and thermotropic mesomorphic properties

An homologous series of 6- O - n -alkyl- alpha -D-galactopyranoses has been prepared. The length of the terminal chains has been varied systematically and the effect on the liquid crystal transition temperatures studied. Most homologues of the series exhibit enantiotropic smectic A* phases. X-ray analysis indicates a lamellar structure for the smectic A* phase with hydrogen-bonded carbohydrate cores at the layer centre, either with no interdigitation of the tilted terminal alkyl chains but with a high degree of chain melting, or with some degree of chain intercalation. The 6- O - n -alkyl- alpha -D-galactopyranoses possess clearing points at higher temperatures than those of the corresponding n -alkyl alpha -D-galactopyranosides. The introduction of a higher degree of hydrogen bonding by the replacement of the oxygen atom in the ether linkage between the chain and the carbohydrate ring by an amide linkage leads to higher transition temperatures. The dependence of the liquid crystalline behaviour on the position of the same alkyl substituent and the nature of the sugar in the pyranose form, as well as on the anomeric configuration of the liquid crystalline carbohydrates with four hydroxy groups, is reported.     

Synthesis and properties of new (−)-menthol-derived chiral liquid crystal compounds with alkyl or alkoxy terminal groups

Two series of chiral mesogenic compounds derived from (?)-menthol with varying length of alkyl or alkoxy terminal groups respectively were designed and synthesised. Their chemical structures were characterised by FT-IR and ¹H-NMR spectra. The thermal properties and optical textures were investigated by differential scanning calorimetry and polarising optical microscopy. Bragg selective reflection spectra of the compounds with the alkoxy chain in the N* phase were measured by ultraviolet/visible spectrometer. The results showed that the alkyl series homologues melt directly to the isotropic phase on heating and display cubic blue phase and focal conic textures of chiral nematic phase on cooling, whereas the alkoxy series displayed oily streak textures with iridescent colours on heating, and platelet textures of blue phase and focal conic textures were observed on cooling cycles. The chain structure and length of the terminal groups have profound influence on the isotropic temperature and a large odd–even effect is observed for the compounds. The selective reflection colours of alkoxy series shifted to longer wavelength with the increasing of temperature.     

Banana-shaped mesogens: mesomorphic properties of seven-ring esters derived from 5-chlororesorcinol

Two new homologous series of seven-ring bent-core compounds derived from 5-chlororesorcinol have been synthesized. Many of the lower homologues in both series exhibit the rectangular columnar B₁ phase. However, the three analogous compounds having long terminal alkyl chains exhibit a switchable lamellar phase, which is different from the usual B₂ phase. Although the ground state structure of the mesophase is antiferroelectric, it shows chiral conglomerates with opposite tilt and polarity. Simultaneously, racemic structures are also seen. The mesophases have been characterized using a combination of polarized light microscopy, X-ray diffraction and electro-optical studies.