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Original Articles

Structure property and mesomorphic behaviour of S-shaped liquid crystal oligomers possessing two azobenzene moieties

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Pages 1283-1292 | Received 05 Jan 2016, Accepted 20 Mar 2016, Published online: 14 Apr 2016

References

  • Goodby JW, Mandle RJ, Davis EJ, et al. What makes a liquid crystal? The effect of free volume on soft matter. Liq Crys. 2015;42:593–622.
  • Imrie CT, Luckhurst GR. Liquid crystal dimers and oligomers. In: Demus D, Goodby J, Gray GW, et al., editors. Handbook of liquid crystals. Vol. 2B. Weinheim: Wiley-VCH; 1998. p. 801–833.
  • Imrie CT. Liquid crystal dimers. Struct Bond. 1999;95:149–192.
  • Imrie CT, Henderson PA. Liquid crystal dimers and oligomers. Curr Opin Colloid Interface Sci. 2002;7:298–311. doi:10.1016/S1359-0294(02)00092-4.
  • Imrie CT, Henderson PA. Liquid crystal dimers and higher oligomers: between monomers and polymers. Chem Soc Rev. 2007;36:2096–2124. doi:10.1039/b714102e.
  • Luckhurst GR. Liquid crystals: a chemical physicist’s view. Liq Crys. 2005;32:1335–1364. doi:10.1080/02678290500423128.
  • Attard GS, Date RW, Imrie CT, et al. Non-symmetric dimeric liquid-crystals – the preparation and properties of the a-(4-cyanobiphenyl-4ʹ-yloxy)-ω-(4-nalkylanilinebenzylidene-4ʹ-oxy)alkanes. Liq Crys. 1994;16:529–581. doi:10.1080/02678299408036531.
  • Yeap GY, Hng TC, Yeap SY, et al. Why do non-symmetric dimers intercalate? The synthesis and characterisation of the α-(4-benzylidene-substituted-aniline-4ʹ-oxy)-ω-(2-methylbutyl-4ʹ-(4″phenyl)benzoateoxy)alkanes. Liq Crys. 2009;36:1431–1441. doi:10.1080/02678290903271504.
  • Donaldson T, Staesche H, Lu ZB, et al. Symmetric and non-symmetric chiral liquid crystal dimers. Liq Crys. 2010;37:1097–1110. doi:10.1080/02678292.2010.494412.
  • Yeap GY, Balamurugan S, Rakesh S. Synthesis and mesomorphic properties of chiral liquid crystal dimers derived from azobenzene and substituted naphthol. Liq Crys. 2013;40:555–563. doi:10.1080/02678292.2013.765608.
  • Henderson PA, Cook AG, Imrie CT. Oligomeric liquid crystals: from monomers to trimers. Liq Crys. 2004;31:1427–1434. doi:10.1080/02678290412331298067.
  • Itahara T. Effect of terminal aryl rings of liquid crystal trimers on liquid crystalline properties. Liq Crys. 2014;41:1034–1041. doi:10.1080/02678292.2014.898343.
  • Henderson PA, Imrie CT. Liquid crystal tetramers: influence of molecular shape on liquid crystal behaviour. Liq Crys. 2005;32:1531–1541. doi:10.1080/02678290500410620.
  • Yelamaggad CV, Achalkumar AS, Rao DSS, et al. Monodispersive linear supermolecules stabilizing unusual fluid layered Phases. Org Lett. 2007;9:2641–2644. doi:10.1021/ol070808p.
  • Blumstein RB, Stickles EM. Synthesis of model compounds of the nematic polyesters poly(2,2ʹ-dimethyl-4,4ʹ-dioxyazoxy-benzenedodecanedioyl). Mol Cryst Liq Cryst Lett. 1982;82:151–159. doi:10.1080/01406568208070136.
  • Cestari M, Diez-Berart S, Dunmur DA, et al. Phase behavior and properties of the liquid-crystal dimer 1 “,7 “-bis(4-cyanobiphenyl-4 ‘- yl) heptane: A twist-bend nematic liquid crystal. Phys Rev E. 2011;84(3). doi:10.1103/PhysRevE.84.031704.
  • Henderson PA, Imrie CT. Methylene-linked liquid crystal dimers and the twist-bend nematic phase. Liq Crys. 2011;38:1407–1414. doi:10.1080/02678292.2011.624368.
  • Borshch V, Kim YK, Xiang J, et al. Nematic twist-bend phase with nanoscale modulation of molecular orientation. Nat Commun. 2013;4:2635. doi:10.1038/ncomms3635.
  • Jansze SM, Martinez-Felipe A, Storey JMD, et al. A twist-bend nematic phase driven by hydrogen bonding. Angew Chem Int Ed. 2015;54:643–646.
  • Wang Y, Singh G, Agra-Kooijman DM, et al. Room temperature heliconical twist-bend nematic liquid crystal. Crystengcomm. 2015;17:2778–2782. doi:10.1039/C4CE02502D.
  • Tschierske C. Liquid crystalline materials with complex mesophase morphologies. Curr Opin Colloid Interface Sci. 2002;7:69–80. doi:10.1016/S1359-0294(02)00014-6.
  • Saez IM, Goodby JW. Supermolecular liquid crystals. J Mater Chem. 2005;15:26–40. doi:10.1039/b413416h.
  • Kumar S. Triphenylene-based discotic liquid crystal dimers, oligomers and polymers. Liq Crys. 2005;32:1089–1113. doi:10.1080/02678290500117415.
  • Imrie CT, Lu ZB, Picken SJ, et al. Oligomeric rod-disc nematic liquid crystals. Chem Commun. 2007;12:1245–1247. doi:10.1039/B614922G.
  • Pal SK, Kumar S, Seth J. Synthesis and characterisation of novel rod-disc oligomers. Liq Crys. 2008;35:521–525. doi:10.1080/02678290802051072.
  • Yamaguchi A, Watanabe M, Yoshizawa A. Odd-even effects in the phase transition behaviour of novel U-shaped liquid crystals. Liq Crys. 2007;34:633–639. doi:10.1080/02678290701292355.
  • Kihara H, Tamaoki N. In situ photochemical conversion from cinnamoyl-functionalized liquid-crystalline monomers to liquid-crystalline dimers. Liq Crys. 2007;34:1337–1347. doi:10.1080/02678290701697454.
  • Yoshizawa A, Nakata M, Yamaguchi A. Phase transition behaviour of novel Y-shaped liquid crystal oligomers. Liq Crys. 2006;33:605–609. doi:10.1080/02678290600617462.
  • Yoshizawa A, Chiba S, Ogasawara F. Synthesis and physical properties of novel liquid crystal oligomers possessing polar terminal groups. Liq Crys. 2007;34:373–379. doi:10.1080/02678290601111440.
  • Kashima S, Takanishi Y, Yamamoto J, et al. Flexible taper-shaped liquid crystal trimer exhibiting a modulated smectic phase. Liq Crys. 2014;41:1752–1761. doi:10.1080/02678292.2014.950353.
  • Yoshizawa A, Kasai H, Ogasawara F, et al. Synthesis and physical properties of novel S-shaped liquid crystal oligomers. Liq Crys. 2007;34:547–553. doi:10.1080/13682820701261991.
  • Ogasawara F, Kasai H, Nagashima Y, et al. Structure-property correlations of novel S-shaped liquid crystal oligomers. Ferroelectrics. 2008;365:48–57. doi:10.1080/00150190802062908.
  • Imrie CT, Henderson PA, Seddon JM. Non-symmetric liquid crystal trimers. The first example of a triply-intercalated alternating smectic C phase. J Mater Chem. 2004;14:2486–2488. doi:10.1039/b404319g.
  • Attard GS, Imrie CT. Trimeric liquid-crystals containing lateral alkyl chains. Liq Crys. 1989;6:387–390. doi:10.1080/02678298908034183.
  • Imrie CT, Stewart D, Rémy C, et al. Liquid crystal tetramers. J Mater Chem. 1999;9:2321–2325. doi:10.1039/a901899i.
  • Nagashima Y, Ogasawara F, Yamamoto J, et al. Molecular organization of preorganized S-shaped oligomers in the liquid crystalline phases. Mol Cryst Liq Cryst. 2009;509:233–244. doi:10.1080/15421400903054527.
  • Al-Hamdani UJ, Gassim TE, Radhy HH. Synthesis and characterization of Azo compounds and study of the effect of substituents on their liquid crystalline Behavior. Molecules. 2010;15:5620–5628. doi:10.3390/molecules15085620.
  • Ooi YH, Yeap GY, Han CC, et al. Non-conventional three-armed star shaped mesogens based on 1,3,5-trisubstituted benzene with azobenzene moieties at the periphery: synthesis, and mesomorphic behaviour. Liq Crys. 2014;41:1017–1033. doi:10.1080/02678292.2014.898341.
  • Dierking I. Texture of liquid crystal. Weinheim: Wiley-VCH; 2003.
  • Demus D, Kölz KH, Sackmann H. Isomorphic relations between crystal-liquid phase.17. Polymorphism of crystal-liquid states of dialkyl para terphenyl-4,4ʹʹ-dicarboxylate-smectic E modifications. Z Phys Chem. 1973;252:93–112.
  • Ooi YH, Yeap GY, Takeuchi D. Synthesis, mesomorphic properties and structural studies on 1,3,5-trisubstitutes benzene-based star-shaped derivatives containing Schiff base ester as the peripheral arm. J Mol Struct. 2013;1051:361–375. doi:10.1016/j.molstruc.2013.08.015.
  • Imrie CT, Luckhurst GR. Liquid crystal trimers. The synthesis and characterisation of the 4,4ʹ-bis[ω-(4-cyanobiphenyl-4ʹ-yloxy)alkoxy]biphenyls. J Mat Chem. 1998;8:1339–1343. doi:10.1039/a801128a.
  • Imrie CT, Henderson PA, Yeap GY. Liquid crystal oligomers: going beyond dimers. Liq Crys. 2009;36:755–777. doi:10.1080/02678290903157455.
  • Marcelis ATM, Koudijs A, Sudhӧlter EJR. Dimer liquid crystals with bent mesogenic units. Liq Crys. 2000;27:1515–1523. doi:10.1080/026782900750018681.
  • Osman F, Yeap GY, Takeuchi D. Synthesis and mesomorphic behaviour of new disulphide bridge 4-n-alkoxybenzylidine-4ʹ-bromoaniline. Liq Crys. 2014;41:106–112. doi:10.1080/02678292.2013.839833.

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