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 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 Synthesis, Mesomorphic, and Solar Energy Characterizations of New Non-Symmetrical Schiff Base Systems

2021 ◽  
Vol 9 ◽  
Author(s):  
Fowzia S. Alamro ◽  
Hoda A. Ahmed ◽  
Sobhi M. Gomha ◽  
Mohamed Shaban
Keyword(s):  
Schiff Base ◽  
Solar Energy ◽  
Methoxy Group ◽  
Energy Gap ◽  
Molecular Structures ◽  
Ortho Position ◽  
Electric Resistance ◽  
Scanning Calorimetry ◽  
Energy Applications ◽  
Terminal Chain

New asymmetrical Schiff base series based on lateral methoxy group in a central core, (E)-3-methoxy-4-(((4-methoxyphenyl)imino)methyl)phenyl 4-alkoxybenzoate (An), were synthesized and their optical and mesomorphic characteristics were investigated. The lateral OCH3group was inserted in the central ring in ortho position with respect to the azomethine linkage. FT-IR, and NMR spectroscopy as well as elemental analyses were used to elucidate their molecular structures. Their mesomorphic behaviors were characterized by polarized optical microscopy (POM) and differential scanning calorimetry (DSC). These examinations indicated that all the designed series were monomorphic and possessed nematic (N) mesophase enantiotropically, except A12 derivative which exhibited monotropic N phase. A comparative study was made between the present investigated series (An) and their corresponding isomers (Bn). The results revealed that the kind and stability of the mesophase as well as its temperature range are affected by the location and special orientation of the lateral methoxy group electric-resistance, conductance, energy-gap, and Urbach-energy were also reported for the present investigated An series. These results revealed that all electrodes exhibit Ohmic properties and electric-resistances in the GΩ range, whereas the electric resistance was decreased from 221.04 to 44.83 GΩ by lengthening the terminal alkoxy-chain to n = 12. The band gap of the An series was reduced from 3.43 to 2.89 eV by increasing the terminal chain length from n = 6 to n = 12 carbons. Therefore, controlling the length of the terminal chain can be used to improve the An series’ electric conductivity and optical absorption, making it suitable for solar energy applications.

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 A method for pet mechanical properties enhancement

2019 ◽  
Vol 10 (8) ◽  
pp. 1725
Author(s):  
Raffaella Aversa ◽  
Relly Victoria Virgil Petrescu ◽  
Antonio Apicella ◽  
Florian Ion Tiberiu Petrescu
Keyword(s):  
Mechanical Properties ◽  
Liquid Crystalline ◽  
Liquid Crystalline Polymers ◽  
Molecular Structures ◽  
Reactive Blending ◽  
Scanning Calorimetry ◽  
Shear Transfer ◽  
Crystalline Polymers ◽  
Reactive Compatibilizer

A method for PET mechanical properties enhancement by reactive blending with HBA/HNA Liquid Crystalline Polymers for in situ highly fibrillar composites preparation is presented. LCP/PET blends were reactively extruded in presence of Pyromellitic Di-Anhydride (PMDA) and then characterized by Differential Scanning Calorimetry, Thermally Stimulated Currents and tensile mechanical properties. Moderate amounts of LCP in the PET (0.5 and 5%) and small amounts of thermo-active and reactive compatibilizer in the blend (0.3%) were found to significantly improve LCP melt dispersion, melts shear transfer and LCP fibril formation and adhesion. An unexpected improvement was probably due to the presence of two distinct phases’ supra-molecular structures involving PET-LCP and PMDA.

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.

Synthesis and Liquid Crystalline Properties of New Chiral Monomers and Polysiloxanes

2013 ◽  
Vol 815 ◽  
pp. 747-751
Author(s):  
Jian She Hu ◽  
Yi Nan Liu ◽  
Ya Ting Song ◽  
Di Wang
Keyword(s):  
Liquid Crystalline ◽  
Structure Property ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Cholesteric Phase ◽  
Crystalline Materials ◽  
H Nmr ◽  
Structure Property Relationships ◽  
Potential Applications ◽  
Liquid Crystalline Materials

To study the structure-property relationships of new chiral liquid crystalline materials based on menthol and explore their potential applications, a monomer 4-(4-allyloxybenzoyloxy) phenyl-4-menthyl-oxyacetyloxybiphenyl-4-carboxylate (LCM) and the corresponding homopolymer (LCP) were synthesized. The chemical structure was characterized by FT-IR and 1H NMR. The liquid crystalline properties were investigated by differential scanning calorimetry, thermogravimetric analysis, polarizing optical microscopy, and X-ray diffraction. The monomer LCM formed a cholesteric phase when a flexible linkage chain was inserted between the mesogenic core and the terminal menthyl groups by reducing the steric effect. The homopolymer LCP exhibited a batonnet texture of a smectic A phase.

Sign in / Sign up

Export Citation Format

Share Document