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501.
After preparing a homologous series of tetrameric mesogenic compounds in which two U-shaped molecules were connected via a rigid benzene derivative or a flexible alkyl chain, we investigated their phase transition behaviour using optical microscopy, differential scanning calorimetry and X-ray diffraction analysis. The compounds possessing an alkyl spacer as the central group exhibited nematic and smectic A phases just as the corresponding U-shaped molecule did. The compound possessing a 1,2-benzene unit as the connecting group showed nematic and smectic A phases, although the compound possessing a 1,3-benzene unit exhibited only an anticlinic smectic C phase. Structure–property relations of the liquid crystalline tetramers are interpreted in terms of preorganised effects of the four mesogenic units. 相似文献
502.
A series of 1-biphenyl-4-alkyl-[1,2,3]-triazole-based liquid crystal compounds were synthesised via a fast and efficient microwave mediated ‘Click Reaction’ and their phase behaviour is presented. Most of the 1-(3-fluorobiphenyl)-4-alkyl-[1,2,3]-triazole compounds exhibited a smectic A phase with relatively low transition temperatures compared to previously examined aryl-triazole-based mesogens. Small angle X-ray scattering measurement indicated the existence of deep smectic phase for some cases. Structural variations gave rise to different phase behaviour in these triazole-based compounds. 相似文献
503.
The phase of a liquid crystal (LC) changing from a nematic phase to a cholesteric (Ch) mesophase is achieved by adding different ratios of chiral dopants S811. By studying the transmission spectrum, we are able to measure the helical pitch in cholesteric phase. The pitch in the mixtures of nematic E7 and chiral dopants S811 as a function of the concentration of the dopant and temperature is investigated. The sensitivity of the selective reflection notch of the cholesteric phase to the thermal tuning depends strongly on the ratios of the chiral dopants. It reveals that the influence of temperature is more profound for those cholesteric liquid crystals (CLCs) which exhibit smectic A (SmA) at lower temperatures. When fitted using Keating's formula, the helical pitch calculated from our experimental results lies on the predicted curve. Optimised ratios of the mixture CLCs for the optimised reflection band with the specified wavelength ranging from 467 nm to 2123 nm are suggested. 相似文献
504.
B.T. Thaker N.J. Chothani Y.T. Dhimmar B.S. Patel D.B. Solanki N.B. Patel 《Liquid crystals》2013,40(5):551-569
Four new mesogenic homologous series, each containing a 6-alkoxy 2-naphthoic acid and Schiff base-ester as central linkage, have been synthesised by esterification of 4-{[(4-hydroxyphenyl) imino] methyl} phenyl 4-propoxy benzoate, 4-{[(4-hydroxyphenyl) imino] methyl} phenyl 4- (pentyloxy) benzoate, 4-{[(4-hydroxyphenyl)imino]methyl}-2-methoxyphenyl 4- nitrobenzoate and 4-{[(4-hydroxyphenyl)imino]methyl}-2-methoxyphenyl 4- chlorobenzoate with different 6-alkoxy 2-naphthoic acid to give Series-A, -B, -C and -D, respectively. These compounds were characterised by elemental analysis, Fourier transform infrared, 1H nuclear magnetic resonance, ultraviolet-visible and mass spectral studies. Their mesomorphic behaviour was studied by polarising optical microscope (POM) with a heating stage. POM data were compared with differential scanning calorimetry thermograms. In Series-A and -B all compounds exhibit mesomorphism. Series-A compounds exhibit a enantiotropic nematic mesophase, while a smectic A mesophase is observed from the butoxy derivative and persists up to the last member of the homologou series. Series-B compounds also exhibit the enantiotropic nematic mesophase, while the smectic A mesophase is observed from the ethoxy derivative and persists up to the last member of the homologou series. The mesomorphic properties of both series are compared with each other and the other structurally related Series-C and –D compounds. In Series-C and -D all compounds exhibit the only nematic mesophase; no smectic mesophase is observed even for higher members of the homologous. The aim of the research was to synthesise and characterise novel liquid crystalline compounds containing 2,6-disubstituted naphthalene and to study their mesomorphic properties. 相似文献
505.
Gordon T. Stewart 《Liquid crystals》2013,40(5):541-557
In our present state of knowledge, it is useful to assume that all matter, in the solar galaxy at least, is composed of atoms and subatomic particles which function independently or interact in accordance with the laws of physics to form molecules, coacervates or other aggregates. For practical purposes, these states of matter are recognizable in the three-dimensional terrestrial world as solids, liquids and gases. This differentiation suffices also for molecular studies but, to understand the properties of mobile organic and especially of living matter fundamentally, it is necessary to investigate and conceptualize how immaterial electromagnetic and electrostatic processes produce changes in state, phase and entropy compatible with self-replication, molecular memory and vitality This possibility exists in the properties of the liquid crystal (LC) as a mesophase in thermal and optical phase transitions, i.e. as an enantiomorphic intermediate form of matter which can form complex, self-replicating, ordered structures and macromolecules, easily recognizable in everyday TV visual displays, electronic communication devices and computers. It is suggested that, in prebiotic terrestrial situations, matter possessing these properties of the LC was a precursor in the evolution of living from inanimate matter and, in the lyotropic form, in the processes of life thereafter. 相似文献
506.
Vladimíra Novotná Věra Hamplová Miroslav Kašpar Natalia Podoliak Damian Pociecha 《Liquid crystals》2013,40(1):14-21
Liquid-crystalline compounds with different numbers of lactate units, n, in the chiral part were synthesised and mesomorphic properties studied. Physical properties were compared with respect to n. In the compound with one lactate unit in the chiral part the TGBA–TGBC–SmC* phase sequence was detected. For two lactate units the antiferroelectric SmC*A phase occurs. Finally, three-lactate material exhibits the tilted hexatic SmI*(F*) phase below the ferroelectric SmC* phase. Dielectric spectroscopy and spontaneous tilt and polarisation were measured. For the three-lactate compound the temperature dependences were analysed in the vicinity of the SmC*–hexatic phase transition, and these properties compared with the theoretically predicted behaviour. 相似文献
507.
MARY E. NEUBERT DAVID G. ABDALLAH Jr. SANDRA S. KEAST JULIE M. KIM SOONNAM LEE RYAN M. STAYSHICH 《Liquid crystals》2013,40(6):711-731
New diphenyldiacetylenes of the type with A, B = H and/or F; m = 0, 1; n = 1–4; and X = C n H2n+1, F, CF3 or CN were synthesized and their mesomorphic properties determined by hot stage polarizing microscopy and DSC. When m = 0, all of these compounds showed only a nematic phase except when X = CF3 when both nematic and smectic A phases were seen. Both clearing and melting temperatures were higher than those reported for substitution with the corresponding alkyl chains but the much larger increase in clearing temperatures produced considerably wider nematic phases. Eutectic mixtures of a few of these olefins yielded nematic materials also having much wider temperature ranges and higher clearing temperatures than the eutectic mixtures of the alkyl compounds, while retaining their high birefringence and low viscosities. Such materials are of interest for beam-steering devices. Four of the diacetylenes with m = 1 (A, B = H) were also prepared (X = C6H13, F, n= 2, 3). When X was C6H13 (n=2), the nematic range was smaller in the 2- than in the 1-olefin but wider than in the alkyl series. When X=F, either no nematic phase or a monotropic one was observed, whereas the 1-olefins gave a much wider nematic phase. Both transition temperatures were lower than those for the corresponding 1-olefin and alkyl analogues. The compound with X=C6H13 and n=2 had a melting temperature below room temperature. 相似文献
508.
Specific textures and their temperature transformations in large temperature interval for the chiral smectic C* mesophase of new liquid crystalline materials, synthesized by our group, have been investigated in detail. Temperature dependences of the pitch of helical structure of the smectic C* mesophase have been determined for these materials. (© 2007 WILEY ‐VCH Verlag GmbH & Co. KGaA, Weinheim) 相似文献
509.
Dr. Bathini Veeraprakash Dr. Gallelli Pratap Dr. Nitin P. Lobo Prof. Krishna V. Ramanathan Dr. Tanneru Narasimhaswamy 《Chemphyschem》2023,24(12):e202300074
Structurally simple rod-like π-conjugated mesogens with thiophene directly connected to phenyl, biphenyl, and fluorenone rings with terminal chains are synthesized respectively. The occurrence of smectic A/smectic C phases is concurred by a hot-stage optical polarising microscope (HOPM), differential scanning calorimetry (DSC), and X-ray diffraction (XRD). The static 1D and 2D 13C nuclear magnetic resonance (NMR) studies in the liquid crystalline phase are carried out to find the alignment-induced chemical shifts (AIS) and 13C−1H dipolar couplings. The orientational order parameters of the mesogens determined from 13C−1H dipolar couplings disclose that the long axis is not only collinear to the C3−C4 bond of the thiophene ring but also for the local axes of phenyl and biphenyl rings. For fluorenone-based mesogen, the molecular biaxiality is found to be high owing to the increased breadth of the molecule. The study unveils that the orientation of thiophene and the phenyl rings is similar in the current mesogens in stark contrast to mesogens, where thiophene is connected to phenyl rings through linking groups. 相似文献
510.
Giancarlo Galli Silvia Gasperetti Massimo Bertolucci Bernard Gallot Federica Chiellini 《Macromolecular rapid communications》2002,23(14):814-818
A new class of fluorinated polymers was prepared by radical ring‐opening homopolymerization of vinylcyclopropane monomers with a perfluorinated (CF2)nF chain (n = 6, 8, or 10). The polymers were in fact copolymers composed of 1,5‐linear and cyclobutane isomer units, the relative content of which depended on n. Surprisingly, they formed liquid‐crystalline mesophases (SmBd and/or SmAd), which was attributed to phase separation of the incompatible fluorocarbon and hydrocarbon components of the repeat unit. 相似文献