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In this article, we designed and synthesized two novel swallow-tailed liquid crystal monomers (M1 and M2) with different chain lengths and rigidities centered on 3,4,5-trihydroxybenzoic acid and two series of side-chain liquid crystals polymers PN1 and PN2. All liquid crystal monomers and polymers were conformed to the molecular designs by FT-IR and NMR. The liquid crystal properties were tested by DSC and POM, and the results showed that M1 and M2 were thermotropic enantiotropic nematic liquid crystals and the side-chain liquid crystal polymers PN1 and PN2 series were typical amorphous liquid crystal polymers. With the increase of monomer content, the glass transition temperatures and clearing points of PN1 and PN2 series enhanced. With the increase of the number of mesogens in the liquid crystal monomer, the rigidity was enhanced, and the liquid crystal performance of the polymer was better. [ABSTRACT FROM AUTHOR]

In this paper, we designed and synthesised three Schiff base mesogenic units X-YP and six Y-shaped liquid crystal oligomers X-AYP and X-BYP (×= -CH3O, -CH3, -Cl). Molecular structures of the prepared compounds were confirmed via FT-IR, 1H NMR and elemental analysis. The mesomorphic properties were investigated by differential scanning calorimetry (DSC) and polarised light microscopy (POM). The photochemical properties of Y-shaped liquid crystal oligomers were preliminarily studied by UV-Vis spectrum. The results indicated that X-YP containing OCH3 and Cl substituents exhibited mesophase, while X-YP with CH3 substituent was non-mesogenic. The synthesized Y-shaped liquid crystals X-AYP and X-BYP both had liquid crystal properties and exhibited nematic phase during heating and cooling, which belonged to thermotropic enantiotropic nematic liquid crystals. The polarity of the terminal groups and the number of mesogenic units had a significant effect on the mesophase behaviour of Y-shaped liquid crystals. The absorption intensities of X-AYP and X-BYP in the UV spectra were affected by the terminal substituents. [ABSTRACT FROM AUTHOR]

In this paper, we designed and synthesised three H-shaped liquid crystal monomers ABOP-n (n = 4,6,8) and a straight-chain liquid crystal monomer M. Then, we used three H-shaped liquid crystal monomers as crosslinking agents, which were graft-copolymerised with M and polymethylhydrosiloxane (PMHS), respectively, to synthesise three series of liquid crystal elastomers P1–P3. The products were structurally well characterised by elemental analysis, 1HNMR, and FT-IR. The phase behaviours were investigated using the polarising microscope (POM) and differential scanning calorimetry (DSC). The results showed that ABOP-8, ABOP-6, ABOP-4 and M were thermotropic enantiotropic nematic liquid crystals, exhibiting schlieren texture during heating, and spherulite texture and schlieren texture during cooling. The photochemical properties of H-shaped liquid crystal monomers were preliminarily studied by UV-Vis spectra, and it was found that they have good photosensitivity. Both the P1–P3 series were typical non-crystalline polymers with anisotropic coloured textures. With the increase of crosslinking monomer content, the glass transition temperature of the P1–P3 series both increased, while the isotropic temperature showed a trend of first decreasing and then increasing. [ABSTRACT FROM AUTHOR]

In this paper, we designed and synthesised two azo liquid crystal monomers (M1 and M2) and a chiral liquid crystal monomer N, followed by side-chain graft copolymerisation with polymethylhydrosiloxane (PMHS) to synthesize comb-like liquid crystalline polymers PN1 and PN2. The structures of all liquid crystal monomers and polymers conform to the molecular designs by FT-IR and 1H NMR. The liquid crystal properties were tested by DSC and POM, and the results showed that M1 and M2 were thermotropic enantiotropic nematic liquid crystals and N was a thermotropic enantiotropic cholesteric liquid crystal. Both the PN1 and PN2 series were amorphous polymers. The PN1 and PN2 series exhibited a typical Grand-jean texture. The glass transition temperature and isotropic temperature of the PN1 and PN2 series decreased first and then increased with the increase of azo monomer M content. And the glass transition temperature and isotropic temperature of the PN1 series were higher than the PN2 series. Both the PN1 and PN2 series had good thermal stability. The mesophase range of the PN1 series was 173.5°C~181.5°C, and the PN2 series was 162.5°C~172.9°C. [ABSTRACT FROM AUTHOR]

Design and synthesis a series of azo multi-arm liquid crystal monomers (M1-M3) with cholic acid as the chiral core, followed by side chain graft copolymerisation with polymethylhydrosiloxane (PMHS) to synthesise the liquid crystal polymer PM series. All liquid crystal monomers and polymers were conformed to the molecular design in structure by FT-IR and NMR. The liquid crystal performance was tested by DSC and POM, and the results revealed that M1 and M2 were thermotropic enantiotropic cholesteric phase liquid crystals. Liquid crystal monomer M3 has no liquid crystal behaviour in both the up and down temperature processes. Polymers of the PM series exhibited different liquid crystal phases depending on the monomer content, with Grand-Jean texture at lower percentage and oil filament texture at higher percentage. The glass transition temperature and melting temperature decrease progressively with the increase in the liquid crystal monomer content, as opposed to the isotropic temperature. [ABSTRACT FROM AUTHOR]

Two series of symmetric LC dimers with the same rigid group and different fluorine terminal group (F and F3C) have been synthesised by varying the length of flexible spacers, termed 1 F series (1 F-4, 1 F-6, 1 F-8) and 3 F series (3 F-4, 3 F-6, 3 F-8). Chemical structures and LC properties of the six symmetric LC dimers were characterised by Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance hydrogen spectrometer (1H NMR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and polarised optical microscopy (POM). The 1 F series dimers only show nematic phase. While for 3 F series, smectic phase appeared, and with the increase of flexible spacers, the smectic phase is dominant. For the formation of smectic phase of 3 F series, the larger intermolecular transverse force coming from CF3 may be the driving force, and the long flexible spacer makes it possible. The melting temperatures of the 1 F series and 3 F series gradually decrease as the length of the flexible spacer increases, respectively, indicating that molecular rigidity has a greater influence on the melting temperatures. The melting temperatures of the 3 F series dimers decrease faster, which may attribute to the influence of CF3 on the conformation of the dimers. [ABSTRACT FROM AUTHOR]

A series of star-shaped liquid crystal (LC), respectively, based on phloroglucinol, pentaerythritol and glucose as cores, rod-shaped molecules (MeOSBAA, MeSBAA and ClSBAA) containing a schiff base as mesogenic mesogen were synthesised. The molecular structures were confirmed by FT-IR and 1H-NMR techniques. The LC textures and thermal phase behaviours were investigated by polarising optical microscopy and differential scanning calorimetry. The results showed that MeOSBAA and ClSBAA were thermally enantiotropic liquid crystals. Three-arm star LC macromolecules X-SBA3E and four-arm star LC macromolecules X-SBA4E were found to display enantiotropic nematic liquid crystals behaviour. While the five-arm star-shaped chiral LC molecules X-SBA5E exhibited enantiotropic chiral nematic phase. [ABSTRACT FROM AUTHOR]

Cholesteric liquid crystals with selective reflection have important applications in the field of light control and optical thin films. In this study, a series of side-chain cholesteric liquid-crystal polymers (named as PPL series) was synthesised by a one-step hydrosilylation reaction among monomer LA containing cholesterol group, monomer LB containing D(+)-camphoric acid group and monomer LG containing cyano group. The chemical structures and the mesogenic properties of the monomers and polymers were determined by usual test methods. Testing results showed that PPL series polymers had excellent thermal stability and wide range of mesophases. As the content of monomer LB increased, PPL1-PPL6 could be observed colourful Grandjean textures and good selective reflection. The optical rotation experiment indicated that the rotation direction of the PPL series was consistent with that of the monomer LB, and the specific rotation was linearly related to the content of the monomer LB. [ABSTRACT FROM AUTHOR]

A new series of glassy chiral-nematic liquid crystals P-ChxNy, were synthesised by hydrosilylation reaction of chiral mesogenic monomer Ch and nematic monomer N grafted onto polymethylhydrosiloxane. The mesomorphic properties, phase behaviour and selective reflection were studied by differential scanning calorimetry (DSC), polarising optical microscopy (POM), and UV-VIS spectrum. Both the Tg and Tc gradually increased as the amount of unit Ch in the copolymer increased. A series of morphologically stable, glassy chiral-nematic liquid crystals were obtained. Among these copolymers, the well-oriented glassy film of the polymer P-Ch4N3 exhibited a selective reflection band centred at approximately 532 nm with green reflected colour below Tg. Preparation and optical properties of linear polysiloxane-based glassy cholesteric liquid crystals with green reflected colour. [ABSTRACT FROM AUTHOR]

This paper designed and synthesised a series of V-shaped liquid crystal molecules (X-SBAnE) with resorcinol as the core and Schiff base as the mesogenic arms (X-SBAAn). The effects of polarity of terminal groups (X=-CH3O,-CH3,-Cl) and length of flexible chain (n = 4,6,8) on mesogenic ranges were discussed. The chemical structure of X-SBAAn and X-SBAnE was studied using FT-IR and 1H-NMR while their thermal behaviour and mesogenic ranges were investigated via differential scanning calorimetry (DSC) and polarising optical microscopy (POM). The results indicated that X-SBAAn containing OCH3 and Cl substituents exhibited mesophase except for the analogue having CH3 substituent which was found to be non-mesogenic. All of the synthesised X-SBAnE had liquid crystal properties and exhibited nematic phases in heating and cooling. The length of the flexible spacers and terminal groups significantly influenced their mesogenic ranges. [ABSTRACT FROM AUTHOR]

A series of symmetric liquid crystal (LC) dimers with the same chiral core (S)-1-phenylethane-1,2-diol ((S)-PE) have been synthesised, termed TBDA-(S)-PE, 3F3B-(S)-PE, 3F2B-(S)-PE, 1F3B-(S)-PE, 1F2B-(S)-PE, respectively. Chemical structures and LC properties of the five symmetric LC dimers were characterised by Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance hydrogen spectrometer (1H NMR), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), X-ray diffraction (XRD) and polarised optical microscopy (POM). TBDA-(S)-PE displayed enantiotropic chiral smectic A (SmA*) phase while 3F3B-(S)-PE, 3F2B-(S)-PE, 1F2B-(S)-PE all displayed enantiotropic chiral nematic (N*) phase and 1F3B-(S)-PE displayed monotropic N* phase. The results indicated that the removal of the flexible spacers between the rigid mesogenic arm and the chiral core facilitated the formation of the N* phase. When the rigid mesogenic units are connected to the chiral core directly, the structure of the terminal fluorine group and the rigidity of the mesogenic unit played certain influence on the thermal properties of the LC dimers, but did not change the type of mesomorphic phase. Compared to 3F3B-(S)-PE and 1F3B-(S)-PE, 3F2B-(S)-PE and 1F2B-(S)-PE displayed wider LC ranges, respectively, suggesting molecular regularity had greater influence on LC-isotropic (I) transition temperature. [ABSTRACT FROM AUTHOR]

In this study, we synthesised two series of cholesteric liquid crystal polymers CPQ and CPZ series. First, we prepared four different monomers ML1 containing a cholesteryl group, ML2 containing a cyano group, ML3 containing a phenolic hydroxyl group and ML4 containing isosorbide with azo groups. With the polymethylsiloxanes as the main chain, CPQ series were then synthesised by copolymerisation among the monomers ML1, ML2 and ML3 and CPZ series were synthesised by esterification between the CPQ series and the monomer ML4. 1HNMR and FT-IR spectra confirmed the chemical structures of all the monomers and polymers. The mesomorphic behaviours and thermal properties were investigated by TGA, DSC, POM and XRD. Both the CPQ and CPZ series exhibited excellent thermal stability and reversible phase transitions, as well as interesting Grandjean textures under POM. CPZ series showed higher optical activity than CPQ series due to the introduction of the isosorbide group and the azo group, which could tune the pitch to make Bragg selective reflection appear more easily. UV–Vis spectra investigated the photoresponse behaviours of CPZ series thoroughly. [ABSTRACT FROM AUTHOR]

Two series of novel four-arm azobenzene liquid crystal molecules were designed and synthesized, and their mesophase properties, photo-induced transition were studied. Two series of mesogenic arms were screened with different length of flexible chain (the carbon number n of flexible chain is 4, 6, 8, 10) using methoxy and nitro as terminal substituents R. The four-arm azobenzene LCs were synthesized by introducing the mesogenic arms into cholic acid. FACAE-O-n, FACAE-N-n all belonged to photosensitive thermotropic enantiotropicnematic LCs. For methoxyl series, melting transitions (Tm), liquid crystal-isotropic transitions (Ti) and mesogenic ranges decreased with the increase of carbon numbers in flexible chain both on heating and cooling. The mesophase performance of FACAE-O-4 was the most excellent. For nitro series, Tm and Ti on heating and cooling decreased with the increase of carbon numbers. Nevertheless, mesogenic ranges increased with the increase of carbon numbers only on heating. The cooling mesogenic ranges showed a trend of rising firstly and then falling, reaching the maximum 103.1oC (n=8). Under ultraviolet irradiation, there was no red shift. The intensity of maximum absorption has changed with the increase of ultraviolet irradiation time. After photo-induced, Tm and Ti on heating and cooling of the four-arm LCs decreased, and the mesogenic ranges became shorter. [ABSTRACT FROM AUTHOR]