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Articles

Mesophase behavior of four ring ester/azomethine/ester liquid crystals in pure and mixed states

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Pages 1395-1402 | Received 07 Dec 2021, Accepted 31 Jan 2022, Published online: 03 Mar 2022

References

  • Sudhakar S, Narasimhaswamy T, Srinivasan KSV. Synthesis, characterization and thermal properties of 4, 4’-bis (4-n-alkoxybenzoyloxy) benzylideneanilines and bis (4-benzylidene-4’-n-alkoxyaniline) terephthalates. Liq Cryst. 2000;27(11):1525–1532‏.
  • Ahmed NH, Saad GR, Ahmed HA, et al. New wide-stability four-ring azo/ester/Schiff base liquid crystals: synthesis, mesomorphic, photophysical, and DFT approaches. RSC Adv. 2020;10:9643–9656.
  • Saha SK, Paul MK. Mesomorphic and photophysical behaviour of 1, 3, 4-oxadiazole based hockey stick reactive mesogens. Liq Cryst. 2019;46:386–396.
  • Ong L-K, Ha S-T, Yeap G-Y, et al. Heterocyclic pyridine-based liquid crystals: synthesis and mesomorphic properties. Liq Cryst. 2018;45:1574–1584.
  • Quan -Y-Y, Wang D, He -Q-Q, et al. V-shaped Schiff’s base liquid crystals based on resorcinol: synthesis and characterisation. Liq Cryst. 2020;47:737–749.
  • Yeap G-Y, Osman F, Imrie CT. Non-symmetric dimers: effects of varying the mesogenic linking unit and terminal substituent. Liq Cryst. 2015;42:543–554.
  • Fritsch L, Lavayen V, Merlo AA. Photochemical behaviour of Schiff base liquid crystals based on isoxazole and isoxazoline ring. A kinetic approach. Liq Cryst. 2018;45:1802–1812.
  • Paterson DA, Crawford CA, Pociecha D, et al. The role of a terminal chain in promoting the twist-Bend nematic phase: the synthesis and characterisation of the 1-(4-cyanobiphenyl-4 ‘-yl)-6-(4-alkyloxyanilinebenzylidene-4 ‘-oxy)hexanes. Liq Cryst. 2018;45:2341–2351.
  • Walker R, Pociecha D, Strachan GJ, et al. Molecular curvature, specific intermolecular interactions and the twist-Bend nematic phase: the synthesis and characterisation of the 1-(4-cyanobiphenyl-4-yl)-6-(4-alkylanilinebenzylidene-4-oxy)hexanes (CB6O.m). Soft Matt. 2019;15:3188–3197.
  • Walker R, Majewska M, Pociecha D, et al. Twist-Bend nematic glasses: the synthesis and characterisation of pyrene-based nonsymmetric dimers. Chemphyschem. 2021;22:461–470.
  • Forsyth E, Paterson DA, Cruickshank E, et al. Liquid crystal dimers and the twist-Bend nematic phase: on the role of spacers and terminal alkyl chains. J Mol Liq. 2020;320(15):114391.
  • Alamro FS, Gomha SM, Shaban M, et al. Optical investigations and photoactive solar energy applications of new synthesized Schiff base liquid crystal derivatives. Sci Rep. 2021;11(1):1–11.
  • Al-Mutabagani L, Alshabanah LA, Ahmed HA, et al. Synthesis, optical and DFT characterizations of laterally fluorinated phenyl cinnamate liquid crystal non-symmetric system. Symmetry. 2021;13(7):1145.
  • Gomha SM, Ahmed HA, Shaban M, et al. Synthesis, optical characterizations and solar energy applications of new Schiff base materials. Materials. 2021;14(13):3718.
  • Altowyan AS, Ahmed HA, Gomha SM, et al. Optical and thermal investigations of new Schiff base/Ester systems in pure and mixed states. Polymers. 2021;13(11):1687.
  • Khushaim MS, Alalawy HH, Naoum MM, et al. Experimental and computational simulations of nematogenic liquid crystals based on cinnamic acid in pure and mixed state. Liq Cryst. 2021;48(11):1493–1504.
  • Mandle RJ, Sebastian N, Martinez-Perdiguero J, et al. On the molecular origins of the ferroelectric splay nematic phase. Nat Commun. 2021;12:4962.
  • Mandle RJ, Cowling SJ, Goodby JW. Rational design of rod-like liquid crystals exhibiting 9-two nematic phases. Chem A Eur J. 2017;23:14554–14562.
  • Manabe A, Bremer M, Kraska M. Ferroelectric nematic phase at and below room temperature. Liq Cryst. 2021;48:1079–1086.
  • Brown S, Cruickshank E, Storey JMD, et al. Multiple polar and non-polar nematic phases. Chemphyschem. 2021;22(24):2506–2510.
  • Demus DJ, Goodby GW, and Gray HW. Spi-eSS, and V, Vill, handbook of liquid crystals. Vol. 1. Weinheim: Wiley-VCHI preSS; 1998.
  • Kelker H, Scheurle B. Eine flüssig‐kristalline (nematische) Phase mit besonders niedrigem Erstarrungspunkt. Angew Chem. 1969;81:903–904.
  • Goodby JW. Nano-objects-sculpting and shape in molecular material design (The Pierre Gilles de Gennes ILCS prize lecture). Liq Cryst. 2019;46:1901–1924.
  • Mandle RJ, Stock N, Cowling SJ, et al. Condensation of free volume in structures of nematic and hexatic liquid crystals. Liq Cryst. 2019;46:114–123.
  • El-Atawy AM, Alhaddad OA, Ahmed HA. Experimental and geometrical structure characterizations of new synthesized laterally fluorinated nematogenic system. Liq Cryst. 2021;48(15):2106–2116.
  • Ahmed HA, El-Atawy AM. Synthesis, mesomorphic and geometrical approaches of new non-symmetrical system based on central naphthalene moiety. Liq Cryst. 2021;48(14):1940–1952.
  • Hagar M, Ahmed H, Saad G. Synthesis and mesophase behaviour of Schiff base/ester 4-(arylideneamino) phenyl-4 ″-alkoxy benzoates and their binary mixtures. J Mol Liq. 2019;273:266–273.
  • Huang -C-C, Hsu -C-C, Chen L-W, et al. The effect of position of (S)-2-octyloxy tail on the formation of frustrated blue phase and antiferroelectric phase in Schiff base liquid crystals. Soft Matter. 2014;10:9343–9351.
  • Ahmed HA, Mansour E, Hagar M. Mesomorphic study and DFT simulation of calamitic Schiff base liquid crystals with electronically different terminal groups and their binary mixtures. Liq Cryst. 2020;47(14–15):2292–2304.
  • Abberley JP, Killah R, Walker R, et al. Heliconical smectic phases formed by achiral molecules. Nat Commun. 2018;9:228.
  • Salamonczyk M, Vaupotic N, Pociecha D, et al. Multi-level chirality in liquid crystals formed by achiral molecules. Nat Commun. 2019;10:1922.
  • Ahmed H, Hagar M, Saad G. Impact of the proportionation of dialkoxy chain length on the mesophase behaviour of Schiff base/ester liquid crystals; experimental and theoretical study. Liq Cryst. 2019;46:1611–2016.
  • Ahmed NH, Saad GR, Ahmed HA, et al. New wide-stability four-ring azo/ester/Schiff base liquid crystals: synthesis, mesomorphic, photophysical, and DFT approaches. RSC Adv. 2020;10(16):9643–9656‏.
  • Ahmed H, Hagar M, Alhaddad O. New chair shaped supramolecular complexes-based aryl nicotinate derivative; mesomorphic properties and DFT molecular geometry. RSC Adv. 2019;9:16366–16374.
  • Alamro FS, Ahmed HA, Mostafa AM, et al. Thermal and mesomorphic investigations of 1: 1 supramolecular assemblies of 4-[(4-(n-alkoxy) phenylimino) methyl] benzoic acids having symmetrical and un-symmetrical terminal chain lengths. Symmetry. 2021;13(10):1785.
  • Alamro FS, Ahmed HA, Popoola SA, et al. Synthesis, phase behavior and computational simulations of a pyridyl-based liquid crystal system. Molecules. 2021;26(21):6416.
  • Gray, GW. Gray molecular structure and the properties of liquid crystals. London (UK): Academic press; 1962.
  • Imrie C, Taylor L. The preparation and properties of low molar mass liquid crystals possessing lateral alkyl chains. Liq Cryst. 1989;6(1):1–10.
  • Walker R, Pociecha D, Storey JMD, et al. Remarkable smectic phase behaviour in odd-membered liquid crystal dimers: the CT6O.m series. J Mat Chem C. 2021;9:5167–5173.
  • Date RW, Imrie CT, Luckhurst GR, et al. Smectogenic dimeric liquid crystals. The preparation and properties of the α, ω-bis (4-n-alkylanilinebenzylidine-4′-oxy) alkanes. Liq Cryst. 1992;12(2):203–238.
  • Ghedini M, Pucci D, Viñuales A. Cyclopalladated azo-and azoxybenzene mononuclear complexes containing a chiral chelating ligand. Mol Cryst Liq Cryst. 2007;465(1):59–70.
  • Naoum M, Fahmi A, Alaasar M, et al. Effect of exchange of terminal substituents on the mesophase behavior of laterally methyl substituted phenyl azo benzoates in pure and mixed systems. Thermochim acta. 2011;525:78–86.

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