scholarly journals Thermotropic and lyotropic behaviour of new liquid-crystalline materials with different hydrophilic groups: synthesis and mesomorphic properties

2013 ◽  
Vol 9 ◽  
pp. 425-436 ◽  
Author(s):  
Alexej Bubnov ◽  
Miroslav Kašpar ◽  
Věra Hamplová ◽  
Ute Dawin ◽  
Frank Giesselmann
Keyword(s):  
Liquid Crystalline ◽  
Molecular Structures ◽  
Scanning Calorimetry ◽  
Crystalline Materials ◽  
Smectic Phases ◽  
Chiral Nematic ◽  
Nematic Phases ◽  
Liquid Crystalline Materials ◽  
Hydroxy Groups ◽  
Mesomorphic Properties

Several new calamitic liquid-crystalline (LC) materials with flexible hydrophilic chains, namely either hydroxy groups or ethylene glycol units, or both types together, have been synthesized in order to look for new functional LC materials exhibiting both, thermotropic and lyotropic behaviour. Such materials are of high potential interest for challenging issues such as the self-organization of carbon nanotubes or various nanoparticles. Thermotropic mesomorphic properties have been studied by using polarizing optical microscopy, differential scanning calorimetry and X-ray scattering. Four of these nonchiral and chiral materials exhibit nematic and chiral nematic phases, respectively. For some molecular structures, smectic phases have also been detected. A contact sample of one of the prepared compounds with diethylene glycol clearly shows the lyotropic behaviour; namely a lamellar phase was observed. The relationship between the molecular structure and mesomorphic properties of these new LCs with hydrophilic chains is discussed.

scholarly journals Perhydroazulene-based liquid-crystalline materials with smectic phases

2012 ◽  
Vol 8 ◽  
pp. 403-410 ◽  
Author(s):  
Zakir Hussain ◽  
Henning Hopf ◽  
S Holger Eichhorn
Keyword(s):  
Liquid Crystalline ◽  
X Ray Diffraction ◽  
Core System ◽  
Crystalline Materials ◽  
Smectic Phases ◽  
Differential Scanning Colorimetry ◽  
Temperature Ranges ◽  
Nematic Phases ◽  
Liquid Crystalline Materials ◽  
Mesomorphic Properties

New liquid-crystalline materials with a perhydroazulene core were synthesized and the stereochemistry of these compounds was investigated. The mesomorphic properties of the new LC compounds were investigated by differential scanning colorimetry, polarizing optical microscopy and X-ray diffraction. We report here on the LC properties of nonchiral materials, which predominantly exhibit smectic phases and display nematic phases only within narrow temperature ranges. The dependence of the mesogenic behavior of the new materials on the stereochemistry of the core system was also investigated. All newly synthesized compounds were fully characterized by the usual spectroscopic and analytical methods.

scholarly journals Chiral Photoresponsive Liquid Crystalline Materials Derived from Cyanoazobenzene Central Core: Effect of UV Light Illumination on Mesomorphic Behavior

Crystals ◽  
2020 ◽  
Vol 10 (12) ◽  
pp. 1161
Author(s):  
Anna Poryvai ◽  
Alexej Bubnov ◽  
Michal Kohout
Keyword(s):  
Liquid Crystalline ◽  
Uv Light ◽  
Structural Type ◽  
Optical Microscope ◽  
Light Illumination ◽  
Aromatic System ◽  
Scanning Calorimetry ◽  
Crystalline Materials ◽  
Liquid Crystalline Materials ◽  
Mesomorphic Properties

One of the most frequently utilized liquid crystalline (LC) materials is a rod-like (calamitic) compound 4-cyano-4′-pentylbiphenyl (5-CB). The main objective of this work is to enhance its functionality by introducing a photoresponsive diazenyl spacer in the aromatic core and replace the non-chiral pentyl chain with various chiral alkyl carboxylate units. The mesomorphic properties of the prepared materials have been studied using polarizing optical microscopy and differential scanning calorimetry. It has been found that materials with an extended aromatic system possess the liquid crystalline behavior. The studied LC materials have shown mesophases at lower temperatures than previously reported analogous substances. Furthermore, one of them exhibits a chiral orthogonal frustrated twist grain boundary smectic phase, which has not been previously observed for this structural type of materials. We also investigated photoresponse of the mesophases under illumination with UV-light (365 nm) using a polarizing optical microscope. A non-conventional photoresponse of the prepared materials in a crystalline phase is presented and discussed.

scholarly journals Synthesis, Phase Behavior and Computational Simulations of a Pyridyl-Based Liquid Crystal System

Molecules ◽  
2021 ◽  
Vol 26 (21) ◽  
pp. 6416
Author(s):  
Fowzia S. Alamro ◽  
Hoda A. Ahmed ◽  
Saheed A. Popoola ◽  
Asmaa Aboelnaga
Keyword(s):  
Liquid Crystalline ◽  
Molecular Structures ◽  
Scanning Calorimetry ◽  
Crystalline Materials ◽  
Pyridine Moiety ◽  
Computational Evaluation ◽  
Liquid Crystal System ◽  
Homo And Lumo ◽  
Liquid Crystalline Materials ◽  
Chain Lengths

A homologous set of liquid crystalline materials (Tn) bearing Schiff base/ester linkages were prepared and investigated via experimental and theoretical techniques. Terminal flexible groups of different chain lengths were connected to the end of phenylbenzoate unit while the other end of molecules was attached to the heterocyclic pyridine moiety. The molecular structures of the designed molecules were evaluated by FT-IR, NMR spectroscopic analyses, whereas their mesomorphic properties were investigated by polarized optical microscopy (POM) and differential scanning calorimetry (DSC). They all exhibited dimorphic properties with the exception of the members having the shortest and longest terminal flexible chains (n = 6 and 16), which were monomorphic. The T16 derivative was further found possessing purely smectic A (SmA) mesophase while others have their lengths covered by nematic (N) phase. Moreover, the computational evaluation of the azomethine derivatives was carried out using a DFT approach. The polarity of the investigated derivatives was predicted to be appreciably sensitive to the size of the system. Furthermore, the Frontier molecular orbitals analysis revealed various distributions of electron clouds at HOMO and LUMO levels.

scholarly journals Synthesis and Mesomorphic and Electrical Investigations of New Furan Liquid Crystal Derivatives

2021 ◽  
Vol 9 ◽  
Author(s):  
Laila A. Al-Mutabagani ◽  
Latifah A. Alshabanah ◽  
Sobhi M. Gomha ◽  
Tariq Z. Abolibda ◽  
Mohamed Shaban ◽  
...  
Keyword(s):  
Liquid Crystalline ◽  
Ester Group ◽  
Molecular Structures ◽  
The Other ◽  
Scanning Calorimetry ◽  
Crystalline Materials ◽  
Group A ◽  
Direct Band ◽  
Liquid Crystalline Materials ◽  
Chain Lengths

New homologues set liquid crystalline materials, based on furfural derivatives, namely, (E)-4-((furan-2-ylmethylene)amino)phenyl 4-alkoxybenzoate (Fn), were synthesized and investigated for their mesomorphic and optical characteristics. The prepared homologues series constitutes three derivatives that bear different terminal flexible alkyl chain lengths that vary between 6 and 12 carbons and attached to the phenyl ring linked to the ester group. A furfural moiety is introduced into the other terminal of the molecular structure. Mesomorphic characterizations of the prepared derivatives were measured using differential scanning calorimetry (DSC) and polarized optical microscopy (POM). Molecular structures were elucidated via elemental analyses, FTIR, and NMR spectroscopy. DSC and POM showed that all the synthesized furfural derivatives are purely nematogenic, exhibiting an enantiotropic nematic (N) mesophase, except for the longest chain derivative (F12) that is dimorphic possessing a monotropic smectic A phase and an enantiotropic N mesophase. Results indicated that the incorporation of the heterocyclic furfural ring into the molecular skeleton affected both the mesophase range and stability of investigated homologue. Analysis of the optical properties revealed that the shortest chain compound (F6) possesses two direct band gaps, at 2.73 and 3.64 eV, in addition to higher absorption than the higher homologues, F10 and F12. On the other hand, all the synthesized homologues (Fn) showed Ohmic behaviors, with electric resistances in the GΩ range. The values of the electrical resistances are 103.71, 12.91, and 196.85 GΩ at 0.05 V for F6, F10, and F12, respectively.

scholarly journals Optical investigations and photoactive solar energy applications of new synthesized Schiff base liquid crystal derivatives

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Fowzia S. Alamro ◽  
Sobhi M. Gomha ◽  
Mohamed Shaban ◽  
Abeer S. Altowyan ◽  
Tariq Z. Abolibda ◽  
...  
Keyword(s):  
Solar Energy ◽  
Liquid Crystalline ◽  
Molecular Structures ◽  
Light Illumination ◽  
Electrical Measurements ◽  
Scanning Calorimetry ◽  
Energy Applications ◽  
Meta Position ◽  
Chain Group ◽  
Liquid Crystalline Materials

AbstractNew homologues series of liquid crystalline materials namely, (E)-3-methoxy-4-[(p-tolylimino)methyl]phenyl 4-alkloxybenzoates (I-n), were designed and evaluated for their mesomorphic and optical behavior. The prepared series constitutes three members that differ from each other by the terminally attached alkoxy chain group, these vary between 6 and 12 carbons. A laterally OCH3 group is incorporated into the central benzene ring in meta position with respect to the ester moiety. Mesomorphic characterizations of the prepared derivatives are conducted using differential scanning-calorimetry (DSC), polarized optical-microscopy (POM). Molecular structures were elucidated by elemental analyses and NMR spectroscopy. DSC and POM investigations revealed that all the synthesized derivatives are purely nematogenic exhibiting only nematic (N) mesophase, except for the longest chain derivative (I-12) that is dimorphic possesses smectic A and N phases. Moreover, all members of the group have a wide mesomorphic range with high thermal nematic stability. A comparative study was established between the present derivative (I-6) and their previously prepared isomer. The results indicated that the location exchange of the polar compact group (CH3) influences the N mesophase stability and range. The electrical measurements revealed that all synthesized series I-n show Ohmic behaviors with effective electric resistances in the GΩ range. Under white light illumination, the effective electric conductivity for the compound I-8 is five times that obtained in dark conditions. This derivative also showed two direct optical band gaps in the UV and visible light range. In addition, I-6 has band energy gaps of values 1.07 and 2.79 eV, which are suitable for solar energy applications.

scholarly journals Synthesis and mesomorphic properties of calamitic malonates and cyanoacetates tethered to 4-cyanobiphenyls

2012 ◽  
Vol 8 ◽  
pp. 371-378 ◽  
Author(s):  
Katharina C Kress ◽  
Martin Kaller ◽  
Kirill V Axenov ◽  
Stefan Tussetschläger ◽  
Sabine Laschat
Keyword(s):  
Differential Scanning Calorimetry ◽  
Ambient Temperature ◽  
Liquid Crystalline ◽  
X Ray Diffraction ◽  
Cyanoacetic Acid ◽  
Scanning Calorimetry ◽  
Isotropic Liquid ◽  
X Ray ◽  
Nematic Phases ◽  
Mesomorphic Properties

4-Cyano-1,1'-biphenyl derivatives bearing ω-hydroxyalkyl substituents were reacted with methyl 3-chloro-3-oxopropionate or cyanoacetic acid, giving liquid-crystalline linear malonates and cyanoacetates. These compounds formed monotropic nematic phases at 62 °C down to ambient temperature upon cooling from the isotropic liquid. The mesomorphic properties were investigated by differential scanning calorimetry, polarizing optical microscopy and X-ray diffraction (WAXS).

scholarly journals The Role of Substitution in the Apex Position of the Bent-Core on Mesomorphic Properties of New Series of Liquid Crystalline Materials

Crystals ◽  
2020 ◽  
Vol 10 (9) ◽  
pp. 735 ◽  
Author(s):  
Helena Skopalová ◽  
Petr Špaček ◽  
Václav Kozmík ◽  
Jiří Svoboda ◽  
Vladimíra Novotná ◽  
...  
Keyword(s):  
Liquid Crystalline ◽  
Structural Parameters ◽  
Phase Identification ◽  
Crystalline Materials ◽  
X Ray ◽  
Alkyl Chains ◽  
Calorimetric Measurements ◽  
Liquid Crystalline Materials ◽  
Mesomorphic Properties

We present the synthesis and mesomorphic properties of the new series of bent-core liquid crystals based on 3-hydroxybenzoic acid bearing a lateral substituent in the apex position. Four different substituents of various sizes and electronic properties have been used. We have found that only compounds substituted with fluorine are mesogenic and exhibit one mesophase, whose type differs when prolonging the terminal alkyl chain. For homologues with shorter alkyl chains (octyl, decyl), a columnar B1-type of a mesophase was observed, while materials with longer terminal chains (dodecyl, tetradecyl) exhibited a switchable lamellar SmCAPA phase. Calorimetric measurements, texture observations under a polarizing microscope were performed and electro-optical properties studied. Additionally, dielectric measurements were realized to characterize the molecular dynamics in the SmCAPA phase. All mesogenic compounds were further studied by X-ray measurements to confirm phase identification and obtain more information about their structural parameters.

scholarly journals Mesomorphism behaviour and photoluminescent properties of new asymmetrical 1,2-di(4-alkoxybenzylidene)hydrazines

2019 ◽  
Vol 43 (1-2) ◽  
pp. 67-77 ◽  
Author(s):  
Adil A Awad ◽  
Al-Ameen Bariz OmarAli ◽  
Ahmed Jasim M Al-Karawi ◽  
Zyad Hussein J Al-Qaisi ◽  
Samer Ghanim Majeed
Keyword(s):  
Differential Scanning Calorimetry ◽  
Liquid Crystal ◽  
Liquid Crystalline ◽  
Polarized Light ◽  
Luminescent Properties ◽  
Scanning Calorimetry ◽  
Crystalline Materials ◽  
X Ray ◽  
Step Procedure ◽  
Liquid Crystalline Materials

{1-[4-( n-Alkoxy)]-2-(4’-decyloxy)benzylidene}hydrazines ( n-alkoxy = O(CH2) nH, n = 1–9, 12, 16 or 18), an asymmetrical series of 1,2-disubstituted hydrazines, were prepared in a simple two-step procedure as a part of our continuing work in evaluating hydrophobic azine compounds as photoluminescent liquid crystalline materials. The compounds were characterized spectroscopically and their liquid crystalline behaviour and luminescent properties were evaluated using polarized light optical microscopy, differential scanning calorimetry and X-ray powder diffraction techniques. The studies revealed that all of these compounds are liquid crystalline materials exhibiting photoluminescent properties in the crystalline and liquid crystal states.

Effective control of optical purity by chiral HPLC separation for ester-based liquid crystalline materials forming anticlinic smectic phases

2020 ◽  
pp. 1-11
Author(s):  
Terézia Vojtylová-Jurkovičová ◽  
Petra Vaňkátová ◽  
Magdalena Urbańska ◽  
Věra Hamplová ◽  
David Sýkora ◽  
...  
Keyword(s):  
Liquid Crystalline ◽  
Optical Purity ◽  
Effective Control ◽  
Chiral Hplc ◽  
Hplc Separation ◽  
Crystalline Materials ◽  
Smectic Phases ◽  
Liquid Crystalline Materials
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