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Article

Synthesis and properties of antiferroelectric and/or ferroelectric compounds with the –CH2O group close to chirality centre

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Pages 2245-2255 | Received 11 Feb 2019, Accepted 13 May 2019, Published online: 12 Jun 2019

References

  • Meyer RB, Liébert L, Strzelecki L, et al. Ferroelectric liquid crystals. Le Journal De Physique. 1975;36:69–71.
  • Chandani ADL, Ouchi Y, Takezoe H, et al. Novel phases exhibiting tristable switching. Jpn J Appl Phys. 1989;28:L1261.
  • Galerne Y, Liebert L. Smectic-O films. Phys Rev Lett. 1990;64:906–909.
  • Pozhidaev EP, Vashchenko VV, Mikhailenko VV, et al. Ultrashort helix pitch antiferroelectric liquid crystals based on chiral esters of terphenyldicarboxylic acid. J Mater Chem C. 2016;4:10339.
  • Kurp K, Czerwiński M, Tykarska M, et al. Design of advanced multicomponent ferroelectric liquid crystalline mixtures with submicrometre helical pitch. Liq Cryst. 2017;44(4):748–756.
  • Czerwiński M, Tykarska M, Dąbrowski R, et al. The influence of structure and concentration of cyanoterminated and terphenyl dopants on helical pitch and helical twist sense in orthoconic antiferroelectric mixtures. Liq Cryst. 2012;39(12):1498–1502.
  • Tykarska M, Dąbrowski R, Czerwiński M, et al. The influence of the chiral terphenylate on the tilt angle in pyrimidine ferroelectric mixtures. Phase Transitions. 2012;85(4):364–370.
  • D’havé K, Dahlgren A, Rudquist P, et al. Antiferroelectric liquid crystals with 45° tilt - a new class of promising electro-optic materials. Ferroelectrics. 2000;244:115–128.
  • Lagerwall ST, Dahlgren A, Jagemalm P, et al. Unique electro-optical properties of liquid crystals designed for molecular optics. Adv Funct Mater. 2001;11:87–94.
  • Rudquist P. Orthoconic antiferroelectric liquid crystals. Liq Cryst. 2013;40:1678–1697.
  • Morawiak P, Żurowska M, Piecek W. A long-pitch orthoconic antiferroelectric mixture modified by isomeric and racemic homostructural dopants. Liq Cryst. 2018;45(10):1451–1459.
  • Żurowska M, Dziaduszek J, Szala M, et al. Effect of lateral fluorine substitution far from the chiral center on mesomorphic behaviour of highly titled antiferroelectric (S) and (R) enantiomers. J Mol Liq. 2018;267:504–510.
  • Żurowska M, Dąbrowski R, Dziaduszek J, et al. Influence of alkoxy spacer length and fluorosubstitution of benzene ring on mesogenic and spectral properties of high tilted antiferroelectric 4ʹ-(S)-1-(methylheptyloxycarbonyl)biphenyl-4-yl-4-(2,2,3,3,4,4,4-heptafluorobutoxy)alkoxybenzoates. J Mater Chem. 2011;21:2144–2153.
  • Milewska K, Drzewiński W, Czerwiński M, et al. Design, synthesis and mesomorphic properties of chiral benzoates and fluorobenzoates with direct SmCA*-Iso phase transition. Liq Cryst. 2015;42:1601–1611.
  • Milewska K, Drzewiński W, Czerwiński M, et al. Highly tilted liquid crystalline materials possessing a direct phase transition from antiferroelectric to isotropic phase. Mater Chem Phys. 2016;171(1):33–38.
  • Żurowska M, Morawiak P, Piecek W, et al. A new mesogenic mixture with antiferroelectric phase only at a broad temperature range. Liq Cryst. 2016;43:1365–1374.
  • Żurowska M, Filipowicz M, Czerwiński M, et al. Synthesis and properties of ferro- and antiferroelectric esters with a chiral centre based on (S)-(+)-3-octanol. Liq Cryst. 2019;46(2):299–308.
  • Kula P, Spadło A, Żurowska M, et al. Synthesis of new chiral smectic mesogenes with 4-(2-Phenylethyl)biphenyl and 4-[2-(3-Fluorophenyl)ethyl]biphenyl molecular cores. Synlett. 2010;9:1394–1396.
  • Drzewiński W, Dąbrowski R, Czupryński K. Orthoconic antiferroelectrics. Synthesis and mesomorphic properties of optically active (S)-(+)-4-(1-methylheptyloxycarbonyl) phenyl 4ʹ-(fluoroalkanoyloxyalkoxy)biphenyl-4-carboxylates and 4ʹ-(alkanoyloxyalkoxy)biphenyl-4-carboxylates. Pol J Chem. 2002;76:273–284.
  • Dąbrowski R, Gąsowska J, Otón JM, et al. High tilted antiferroelectric liquid crystalline materials. Displays. 2004;25:9–19.
  • Gąsowska J, Dąbrowski R, Drzewiński W, et al. Comparison of mesomorphic properties in chiral and achiral homologous series of high tilted ferroelectrics and antiferroelectrics. Ferroelectrics. 2004;309:83–93.
  • Kula P, Dąbrowski R, Kenig K, et al. New antiferroelectric compounds from chiral terphenyls. Ferroelectrics. 2006;343:19–26.
  • Żurowska M, Dąbrowski R, Dziaduszek J, et al. Synthesis and mesomorphic properties of chiral esters comprising partially fluorinated alkoxyalkoxy terminal chains and a 1-methylheptyl chiral moiety. Mol Cryst Liq Cryst. 2008;495:145–157.
  • Golofit T, Szala M. Origin of PYX thermal stability investigation with calorimetric and spectroscopic methods. J Therm Anal Calorim. 2017;130(3):2047–2054.
  • Fitas J, Dłubacz A, Fryń P, et al. New ferroelectric and antiferroelectric liquid crystals studied by complementary methods. Liq Cryst. 2017;44(3):566–576.
  • Żurowska M, Czerwiński M. The new high tilt mixtures with antiferroelectric phase at a broad temperature range and a long helical pitch. Liq Cryst. 2017;44(6):1044–1049.
  • Fitas J, Marzec M, Kurp K, et al. Electro-optic and dielectric properties of new binary ferroelectric and antiferroelectric liquid crystalline mixtures. Liq Cryst. 2017;44(9):1468–1476.
  • Fitas J, Jaworska-Gołąb T, Deptuch A, et al. Physical properties of new binary antiferroelectric liquid crystal mixtures. Phase Transitions. 2018;91(2):199–209.
  • Mrukiewicz M, Perkowski P, Garbat K. Dielectric behaviour of binary dual-frequency nematics with low crossover frequencies. Liq Cryst. 2015;42:1036–1042.
  • Perkowski P. Dielectric spectroscopy of liquid crystals. Electrodes resistivity and connecting wires inductance influence on dielectric measurements. Opto-Electron Rev. 2012;20:79–86.
  • Kędziora P. Dielectric relaxation modes in cholesteryl oleyl carbonate observed by non-linear dielectric spectroscopy. Liq Cryst. 2014;41:626–634.
  • Czerwiec JM, Dąbrowski R, Garbat K, et al. Dielectric and electro-optic behaviour of two chiral compounds and their antiferroelectric mixtures. Liq Cryst. 2012;39:1503–1511.
  • Marzec M, Mikułko A, Wróbel S, et al. Dielectric behaviour of para-, ferro- and antiferroelectric liquid crystalline phases. In: Galewski Z, Sobczyk L, editors. Dielectric properties of liquid crystals. Kerala: Tranworld Research Network; 2007: 83–101.
  • Perkowski P, Ogrodnik K, Piecek W, et al. Influence of the bias field on dielectric properties of the SmCA* in the vicinity of the SmC*–smCA* phase transition. Liq Cryst. 2011;38:1159–1167.
  • Mishra A, Żurowska M, Dąbrowski R, et al. Thermodynamical, electrical and electro-optical studies of a room temperature tri-component antiferroelectric liquid crystalline material. Phase Transitions. 2014;87:746–757.
  • Panarin YP, Kalinovskaya O, Vij JK. The investigation of the relaxation processes in antiferroelectric liquid crystals by electro-optic spectroscopy. Appl Phys Lett. 1998;72:1667.
  • Kumari S, Das IML, Dąbrowski R. Thermodynamic and bias field investigation of an antiferroelectric liquid crystal. Physica B. 2012;407:90–95.
  • Panarin YP, Kalinovskaya O, Vij JK. The investigation of the relaxation processes in antiferroelectric liquid crystals by broad band dielectric and electro-optic spectroscopy. Liq Cryst. 1998;25:241–252.
  • Kundu SK, Yagihara S, Yoshizawa A. Dielectric spectroscopy of a smectic liquid crystal. Liq Cryst. 2007;34:981–986.
  • Buivydas M, Gouda F, Andersson G, et al. Collective and non-collective excitations in antiferroelectric and ferrielectric liquid crystals studied by dielectric relaxation spectroscopy and electro-optic measurements. Liq Cryst. 1997;23:723–739.
  • Różański S, Thoen J. Collective and antiferroelectric dielectric modes in a highly tilted three-ring ester. Liq Cryst. 2007;34:519–526.
  • Novotná V, Kašpar M, Hamplová V, et al. Ferroelectric, antiferroelectric and TGB phases in lactic acid derivatives. Liq Cryst. 2012;39:477–486.
  • Perkowski P, Ogrodnik K, Żurowska M, et al. Antiferroelectric SmCA* and ferroelectric SmC* phases in racemic mixture. Phase Transitions. 2013;86:138–146.
  • Perkowski P, Piecek W, Raszewski Z, et al. Precise dielectric spectroscopy of a long pitch orthoconic antiferroelectric working mixture. Mol Cryst Liq Cryst. 2011; 541:191/[429]–200/[438].
  • Perkowski P, Mrukiewicz M, Żurowska M, et al. Dielectric modes in antiferroelectric liquid crystal observed at low temperatures. Liq Cryst. 2013;40:864–870.
  • Perkowski P, Żurowska M. Dielectric properties of a wide-temperature ferroelectric phase in a fluorinated compound. Phase Transitions. 2017;90:808–816.
  • Perkowski P, Mrukiewicz M, Herman J, et al. Dielectric investigation of the liquid crystal compound with the direct SmA*–smCA* phase transition. Liq Cryst. 2016;43:654–663.
  • Takezoe H, Kondo K, Fukuda A, et al. Determination of helical pitch in homeotropic cell of chiral smectic C liquid crystal using F-center laser. Jpn J Appl Phys. 1982;21:L627–L629.
  • Raszewski Z, Kędzierski J, Perkowski P, et al. Refractive indices of the MHPB(H)PBC and MHPB(F)PBC antiferroelectric liquid crystals. Ferroelectrics. 2002;276:289–300.
  • Otón JM, Dąbrowski R, Quintana X, et al. Antiferroelectric and V-shape liquid crystal on silicon microdisplays. Opto-Electron Rev. 2002;10(1):17–21.
  • Takanishi Y, Noma S, Yamamoto J. Novel display mode using dielectric response of antiferroelectric liquid crystals. Appl Phys Express. 2013;6:081701.
  • Geday MA, Poudereux D, Crespo L, et al. Ultrafast AFLC passive display for true 3D images. Ferroelectrics. 2016;495:158–166.

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