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2 - Calamitic-Calamitic LC Dimers

Published online by Cambridge University Press:  23 July 2017

Sandeep Kumar
Affiliation:
Raman Research Institute, Bangalore, India
Santanu Kumar Pal
Affiliation:
Indian Institute of Science Education and Research, Mohali, India
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Summary

INTRODUCTION

Scientific community has done a lot of efforts for controlling molecular ordering of polymer chains through various supramolecular approaches. Among them, a famous approach is keeping the LC molecules a repeating unit of polymer chain. The self-assembling tendency of LC molecules tends to assemble polymer chains into well-ordered structures. A variety of liquid crystalline polymers (LCPs) have been synthesized since the discovery of LCPs in 1923 by Vorlander et al. to achieve the highly ordered polymers.1 The understanding of self-assembly in condensed phases is challenged by these polymers whose interpretation at a molecular level requires experimental investigations as well as the development of new molecular theories. However, the structural heterogeneity inherent in a polymeric system complicates these tasks. An alternative approach is the use of monodisperse low molar mass compounds whose behaviour encapsulates the essential physics of polymeric system for developing a molecular understanding of polymers.

Catalyzed with the motivation to understand LCPs at a molecular level, a wide variety of nonconventional low molar mass compounds were synthesized and shown to support liquid crystallinity. The fact that these compounds were LCs was very surprising because at that time most of the known low molar mass LCs were composed of molecules consisting of a single semirigid anisometric core with alkyl chains. Indeed, it had been widely assumed for many years that such a molecular structure was a prerequisite for the observation of liquid crystallinity. We now know that 1980s evidenced the beginning of the discovery of a rich diversity of structures capable of supporting mesogenic behaviour that has continued to the present day.

Of all these new low molar mass LC discovered during the 1980s, one class that attracted particular attention and which still remains the focus of much research are the so-called LC dimers. An LC dimer is composed of molecules containing two conventional mesogenic groups linked by a flexible spacer. Thus, LC dimers contravened the accepted structure–property relationships for low molar mass mesogens by consisting of molecules having a highly flexible core rather than a semirigid central unit. In this respect, LC dimers represent an inversion of the conventional molecular design for low molar mass mesogens. Several names have been used to refer to these materials including dimesogens or Siamese twins but these have all now been superseded by the preferred term LC dimer.

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Print publication year: 2017

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References

Weiss, R. A. and Ober, C. K. 1990. ‘Liquid-crystalline polymers’. In ACS Symbosium Series , Vol. 235.Google Scholar
Marcos, M., Lomenta, A., Serrano, J. L., and Ezcurra, A. 1992. ‘A ferroelectric liquid crystal dimer: Synthesis and properties’. Adv Mater 4:285–7.Google Scholar
Hird, M., Toyne, K. J., and Gray, G. W. 1993. ‘Palladium-catalysed cross-coupling reactions in the synthesis of some high polarizability materials’. Liq Cryst 14:741–61.Google Scholar
Hird, M., Toyne, K. J., Gray, G. W., Day, S. E., and McDonnell, D. G. 1993. ‘The synthesis and high optical birefringence of nematogens incorporating 2,6-disubstituted naphthalenes and terminal cyanosubstituent’. Liq Cryst 15:123–50.Google Scholar
Gonzales, Y., Ros, M. B., Serrano, J. L., and Pereziubind, A. 1998. ‘Naphthyl benzoates versus phenyl benzoates A molecular structure-liquid crystal and ferroelectric behaviour relationship study’. Liq Cryst 18:751–60.Google Scholar
Gray, G. W., and Windsor, P. A. 1974. Liquid Crystals and Plastic Crystals. Vol. 1. New York/London, U.K.: EllisHorwood: Chichester: Ralsted Press. A Division of John Wiley and Sons, Inc., 327–56.
Gray, G. W. 1962. Molecular Structure and Properties of Liquid Crystals. Vol. 139. London: Academic Press, 206–7.
Demls, D. 1988. ‘Molecular crystals and liquid crystals incorporating nonlinear optics’. Mol Cryst Liq Cryst 165:45–84.Google Scholar
Emsley, J. W., Luckhurst, G. R., Shilstone, G. N., and Sage, I. 1984. ‘The preparation and properties of the α, ω-bis (4, 4′-cyanobiphenyloxy) alkanes: Nematogenic molecules with a flexible core’. Mol Cryst Liq Cryst Lett 102:223–33.Google Scholar
Abe, A., and Furuya, H. 1988. ‘Deuterium NMR analysis of dimer liquid crystals’. Polym Bull 19:403–7.Google Scholar
Abe, A., and Nam, S. Y. 1995. ‘PVT studies on dimer liquid crystals and estimation of transition entropies at constant volume’. Macromolecules 28:90–5.Google Scholar
Abe, A., Furuya, H., Shimizu, R. N., and Nam, S. Y. 1995. ‘Calculation of the conformation entropies of dimer liquid crystals and comparison with the observed transition entropies at constant volume’. Macromolecules 28:96–103.Google Scholar
Dunmur, D. A., and Wilson, M. R. 1988. ‘Lights-cattering study of nematogenic molecules with a flexible core’. J Chem Soc, Faraday Trans II 84:1109–14.Google Scholar
Maeda, Y., Furuya, H., and Abe, A. 1996. ‘High pressure differential thermal analysis of dimer liquid crystals: α, ω-Bis [(4, 4′-cyanobiphenylyl) oxy] alkanes’. Liq Cryst 21:365–71.Google Scholar
Emsley, J. W., Luckhurst, G. R., and Shilstone, G. N. 1984. ‘The orientational order of nematogenic molecules with a flexible core: A dramatic odd–even effect’. Mol Phys 53:1023–8.Google Scholar
Emsley, J. W., Luckhurst, G. R., and Timimi, B. A. 1985. ‘Solute ordering in the α, ω-bis (4, 4′-cyanobiphenyloxy) alkanes: Nematogens with a flexible core. A dramatic odd—even effect’. Chem Phys Lett 114:19–23.Google Scholar
Ionescu, D., Luckhurst, G. R., and de Silva, D. S. 1997. ‘The elastic behaviour of liquid crystal dimers: An ESR investigation of their induced chiral nematic phases’. Liq Cryst 23:833–43.Google Scholar
Heeks, S. K., and Luckhurst, G. R. 1993. ‘On the molecular organisation within the nematic phase of liquid crystal dimmers’. J Chem Soc, Faraday Trans 89:3289–96.Google Scholar
Malpezzi, L., BruÈckner, S., Galbiati, E., Zerbi, G., and Luckhurst, G. R. 1991. ‘The structure of α, ω-bis (4-cyanobiphenyl-4′-oxy) heptane’. Mol Cryst Liq Cryst 195:179–84.Google Scholar
Luckhurst, G. R. 1995. ‘Liquid-crystal dimmers and oligomers—Experimenta and theory’. Macromol Symp 96:1–26.Google Scholar
Jin, J.-I., Chung, Y. S., Lenz, R. W., and Ober, C. 1983. ‘Synthesis and properties of thermotropic compounds with two terminal mesogenic units and a central spacer (II). Homologous series of α1 ω-bis (4-p-substituted phenoxycarbonyl) phenoxyalkanes’. Bull Korean Chem Soc 4:143–48.Google Scholar
Jin, J.-I. 1995. ‘Liquid crystalline behavior of novel dimesogenic compounds’. Mol Cryst Liq Cryst 267:249–65.Google Scholar
Jin, J.-I., and Park, J. H. 1984. ‘Thermotropic compounds with two terminal mesogenic units and a central spacer. 51. Homologous series of polymethylene-α, ω-bis (p-oxybenzylidene aniline)’. Mol Cryst Liq Cryst 110:293–308.Google Scholar
Jin, J.-I., Seong, C. M., and Jo, B. W. 1985. ‘Synthesis and properties of thermotropic compounds with two terminal mesogenic units and a central spacer (VI). Homologous series of α1 ω-bis[4-(psubstituted benzoyloxy)benzoyloxy]alkanes’. Bull Korean Chem Soc 6:40–5.Google Scholar
Jin, J.-I., Kang, J. S. Jo, B. W., and Lenz, R. W. 1983. ‘Synthesis and properties of thermotropic compounds with two terminal mesogenic units and a central spacer III. Homologous series of α1 ω-bis[4- (p-nitrobenzoyloxy)phenoxy]alkanes’. Bull Korean Chem Soc 4:176–80.Google Scholar
Jin, J.-I. 1983. ‘Functionalization of carbon black by surface grafting of polymers’. Polym Prepr Jpn 32:935.Google Scholar
Aquilera, C., Ahmad, S., Bartulin, J., and Muller, H. J. 1988. ‘Synthesis and thermotropic properties of twin mesogens containing a polymethylene spacer Mol Cryst Liq Cryst 162:277–82.Google Scholar
Buglione, J. A., Roviello, A., and Sirigu, A. 1984. ‘Mesophasic properties of low molecular weight model compounds containing two rigid groups connected by a flexible spacer’. Mol Cryst Liq Cryst 106:169–85.Google Scholar
Imrie, C. T., and Luckhurst, G. R. 1998. Low molecular weight liquid crystals, Chap. 10. In Handbook of Liquid Crystals, Vol. 2B, edited by Demus, D., Goodby, J. W., Gray, G. W., Spiess, H. W., and Vill, V.. Weinheim: Wiley-VCH.
Griffin, A. C., and Britt, T. R. 1981. ‘Effect of molecular structure on mesomorphism. 12. Flexible-center Siamese-twin liquid crystalline diesters—A “prepolymer” model’. J Am Chem Soc 103:4957–9.Google Scholar
Date, R. W., Imrie, C. T., Luckhurst, G. R., and Seddon, J. M. 1992. ‘Smectogenic dimeric liquid crystals. The preparation and properties of the α, ω-bis (4-n-alkylanilinebenzylidine-4′-oxy) alkanes’. Liq Cryst 12:203–38.Google Scholar
Gray, G. W. 1979. The Molecular Physics of Liquid Crystals, Chap. 1. Edited by Luckhurst, G. R. and Gray, G. W.. London: Academic Press.
Imrie, C. T. 1996. Polymeric Materials Encyclopedia, Vol. 5. Edited by Salamone, J. C., 3770. Boca Raton: CRC Press.
Jin, J. I., Choi, E. J., Ryu, S. C., and Lenz, R. W. 1986. ‘Thermotropic main chain polyesters with polymethylene spacers and their low molecular weight model compounds—Odd–even effect of polymethylene spacers’. Polym J 18:63–70.Google Scholar
Abe, A., Furuya, H., Nam, S. Y., and Okamoto, S. 1995. ‘Thermodynamics and molecular ordering of carbonate-type dimer liquid crystals with emphasis on the geometrical characteristics of the linking group’. Acta Polym 46:437–44.Google Scholar
Barnes, P. J., Douglass, A. G., Heeks, S. K., and Luckhurst, G. R. 1993. ‘An enhanced odd–even effect of liquid crystal dimers orientational order in the α, ω-bis (4′-cyanobiphenyl-4-yl) alkanes’. Liq Cryst 13:603–13.Google Scholar
Emerson, A. P. J., and Luckhurst, G. R. 1991. ‘On the relative propensities of ether and methylene linkages for liquid crystal formation in calamitics’. Liq Cryst 10:861–8.Google Scholar
Ferrarini, A., Luckhurst, G. R., Nordio, P. L., and Roskilly, S. J. 1994. ‘Prediction of the transitional properties of liquid crystal dimers. A molecular field calculation based on the surface tensor parametrization’. J Chem Phys 100:1460–9.Google Scholar
Luckhurst, G. R. 1985. Recent Advances in Liquid Crystalline Polymers, Chap. 7. Edited by Chapoy, L. L.. London/New York: Elsevier.
Creed, D., Gross, J. R. D., Sullivan, S. L., Griffin, A. C., and Hoyle, C. E. 1987. ‘Effect of molecular structure on mesomorphism. 18.1 Twin dimers having methylene, ethylene oxide and siloxane spacers’. Mol Cryst Liq Cryst 149:185–93.Google Scholar
Chien, J. C. W., Zhou, R., and Lillya, C. P. 1987. ‘Liquid-crystalline compounds and polymers from promesogens’. Macromolecules 20:2340–4.Google Scholar
Sledzinska, I., Bialecka-Florjanczyk, E., and Orzesko, A. 1996. ‘Synthesis and liquid crystalline properties of cholesteryl bisesterimides with poly (ethylene oxide) s as central spacers’. Eur Polym J 32:1345–50.Google Scholar
Hoshino, H., Jin, J.-I., and Lenz, R. W. 1984. ‘Liquid crystalline behavior of polymeric glycols terminated with aromatic diester and diacid mesogenic groups’. J Appl Polym Sci 29:547–54.Google Scholar
Vora, R. A., and Teckchandani, V. R. 1991. ‘Cholesteryl dicarbonates with rigid and flexible spacers’. Mol Cryst Liq Cryst 209:285–9.Google Scholar
Ibn-Elhaj, M., Skoulios, A., Guillon, D., Newton, J., Hodge, P., and Coles, H. J. 1995. ‘Structural characterization of linear dimeric and cyclic tetrameric liquid crystalline siloxane derivatives’. Macromolecules 19:373–8.Google Scholar
Jo, B. W., Lim, T. W., and Jin, J. I. 1988. ‘Synthesis and thermotropic properties of dimesogenic homologous series containing disiloxyl spacer, DI- 4- (P-substituted phenoxycarbonyl) phenoxymethyl tetramethyl disiloxanes’. Mol Cryst Liq Cryst Inc Nonlin Opt 157:57–67.Google Scholar
Jo, B. W., Choi, J. K., Bang, M. S., Chung, B. Y., and Jin, J. I. 1992. ‘Dimesogenic compounds consisting of two aromatic ester or amide type mesogenic units having trifluoromethyl substituents at terminal phenylene rings and a central dimethylenetetramethyldisiloxyl spacer’. Chem Mater 4:1403–9.Google Scholar
Aquilera, C., and Bernal, L. 1984. ‘Thermotropic liquid crystalline bimesogenic molecules with highly flexible oligosiloxane spacer’. Polym Bull 12:383–8.Google Scholar
Dia, A. F., Valdebenito, M. N., Tagle, L. H., and Aguilera, C. 1994. ‘Synthesis and characterization of twin mesogens containing siloxane units as central spacers’. Liq Cryst 16:105–13.Google Scholar
Poths, H., Wischerhoff, E., Zentel, R., Schonfeld, A., Henn, G., and Kremer, F. 1995. ‘From monomeric to polymeric ferroelectric liquid crystals A comparative study of ferroelectric properties’. Liq Cryst 18:811–8.Google Scholar
Hohmuth, A., Schiewe, B., Heinemann, S., and Kresse, H. 1997. ‘Dielectric behaviour of two dimeric liquid crystalline siloxanes’. Liq Cryst 22:211–5.Google Scholar
Ohtake, T., Kanie, K., Yoshizawa, M., et al. 2001. ‘Self-organised ion conductive liquid crystals: Lithium salt complexes of mesogenic dimer molecules exhibiting smectic A phases’. Mol Cryst Liq Cryst 364:589–96.Google Scholar
Robinson, W. K., Carboni, C., Kloess, P., Perkins, S. P., and Coles, H. J. 1998. ‘Ferroelectric and antiferroelectric low molar mass organosiloxane liquid crystals’. Liq Cryst 25:301–7.Google Scholar
Yang, X. T., Takeshita, S., and Yano, S. 2001. ‘Novel mesomorphic phase transitions of symmetric dimeric a,v-bis(49-alkoxy-phenylbenzyl-4-ylthio) perfluoroalkane compounds’. Mol Cryst Liq Cryst 365:1095–102.Google Scholar
Eremin, A., Diele, S., Pelzl, G., Kovalenko, L., Pelz, K., and Weissflog, W. 2001. ‘Polymorphic smectic A phases in perfluoroalkylated mesogenic dimers’. Liq Cryst 28:1451–61.Google Scholar
Imrie, C. T., and Taylor, L. 1989. ‘The preparation and properties of low molar mass liquid crystals possessing lateral alkyl chains’. Liq Cryst 6:1–10.Google Scholar
Jin, J. I., Chung, Y. S., Kang, J. S., and Lenz, R. W. 1982. ‘Synthesis and properties of thermotropic compounds with two terminal mesogenic units and a central spacer’. Mol Cryst Liq Cryst 82:261–6.Google Scholar
Hogan, J. L., Imrie, C. T., and Luckhurst, G. R. 1988. ‘Asymmetric dimeric liquid crystals. The preparation and properties of the α-(4-cyanobiphenyl-4′-oxy)-ω-(4-n-alkylanilinebenzylidene-4′-oxy) hexanes’. Liq Cryst 3:645–50.Google Scholar
Attard, G. S., Date, R. W., Imrie, C. T., Luckhurst, G. R., Roskilly, S. J., Seddon, J. M., and Taylor, L. 1994. ‘Non-symmetric dimeric liquid crystals the preparation and properties of the α-(4-cyanobiphenyl-4′-yloxy)-ω-(4-nalkylanilinebenzylidene-4′-oxy) alkanes’. Liq Cryst 16:529–81.Google Scholar
Attard, G. S., Garnett, S. Hickman, C. G., Imrie, C. T. and Taylor, L. 1990. ‘Asymmetric dimeric liquid crystals with charge transfer groups’. Liq Cryst 7:495–508.Google Scholar
Attard, G. S., Imrie, C. T., and Karasz, F. E. 1992. ‘Low molar mass liquid-crystalline glasses: Preparation and properties of the alpha-(4-cyanobiphenyl-4′-oxy)-omega-(1-pyreniminebenzylidene-4′-oxy) alkanes’. Chem Mater 4:1246–53.Google Scholar
Griffin, A. C., and Vaidya, S. R. 1988. ‘Effect of molecular structure on mesomorphism XX. Unsymmetrical dimeric mesogens’. Liq Cryst 3:1275–8.Google Scholar
Ikeda, T., T. Miyamoto, S. Kurihara, M. Tsukada, and S. Tazuke 1990. ‘Effect of structure of photoresponsive molecules on photochemical phase transition of liquid crystals I. Synthesis and thermotropic properties of photochromic azobenzene derivatives’. Mol Cryst Liq Cryst 182: 357–71.
Blatch, A. E., Fletcher, I. D., and Luckhurst, G. R. 1997. ‘Symmetric and non-symmetric liquid crystal dimers with branched terminal alkyl chains: Racemic and chiral’. J Mater Chem 7:9–17.Google Scholar
Blatch, A. E., Fletcher, I. D., and Luckhurst, G. R. 1995. ‘The intercalated smectic A phase. The liquid crystal properties of the α-(4-cyanobiphenyl-4′-yloxy)-ω)-(4-alkyloxycinnamoate) alkanes’. Liq Cryst 18:801–9.Google Scholar
Pelzl, G., Novak, M., Weissflog, W., and Demus, D. 1987. ‘Binary systems with induced smectic phases due to EDA complex formation’. Cryst Res Technol 22:125–8.Google Scholar
Janietz, D. 1998. ‘Structure formation of functional sheet-shaped mesogens’. J Mater Chem 8:265–74.Google Scholar
Schneider, F., and Sharma, N. K. 1981. ‘Induced smectic phases II. Inf luence of the amino substituent on the induction of smectic phases*’. Z Naturforsch 36a:1086–91.Google Scholar
Demus, D., Pelzl, G., Sharma, N. K., and Weissflog, W. 1981. ‘EDA complexes in liquid crystalline mixed phases’. Mol Cryst Liq Cryst 76:241–51.Google Scholar
Sadowska, K. W., Zywocinski, A., Stecki, J., and Dabrowski, R. 1982. ‘Induced smectic phases. Densities of binary mixtures of 4, 4′-dialkylazoxybenzenes with 4-pentyl-4′-cyanobiphenyl (PCB)’. J Phys (Paris) 43:1673–8.Google Scholar
Boy, A., and Adomenas, P. 1983. ‘Unusual character of some liquid crystal mixtures exhibiting induced smectic mesophases’. Mol Cryst Liq Cryst 95:59–62.Google Scholar
Srikanta, B. S., and Madhusudana, N. V. 1983. ‘Studies on binary mixtures of systems which exhibit a maximum as well as a minimum in the AN transition boundary’. Mol Cryst Liq Cryst 99:203–21.Google Scholar
Oh, C. S. 1977. ‘Induced smectic mesomorphism by incompatible nematogens’. Mol Cryst Liq Cryst 42:1–14.Google Scholar
Schroeder, J. P., and Schroeder, D. C. 1968. ‘Liquid crystals. I. Stable smectic mixtures of 4,4′-di-nhexyloxyazoxybenzene and p-nitro-substituted aromatic compounds’. J Org Chem 33:591–7.Google Scholar
Araya, K., and Matsunaga, Y. 1980. ‘Liquid crystal formation in binary systems. II. Induction of nematic and smectic phases by electron donor–acceptor interaction between the p-dimethylamino and p-nitro derivatives of N-benzylideneaniline’. Bull Chem Soc Jpn 53:3079–84.Google Scholar
Araya, K., and Matsunaga, Y. 1981. ‘Mesophases induced by molecular complexing’. Mol Cryst Liq Cryst 67:153–63.Google Scholar
Araya, K., and Matsunaga, Y. 1981. ‘Liquid crystal formation in binary systems. III. Effect of the central double bond linkage on the induction of nematic liquid crystals’. Bull Chem Soc Jpn 54:2430–4.Google Scholar
Homura, N., Matsunaga, Y., and Suzuki, M. 1985. ‘Mesophases induced in the binary systems consisting of the 4-dimethylamino- 4-alkoxy and 4-nitro-4-alkoxy derivatives of N-benzylideneaniline’. Mol Cryst Liq Cryst 131:273–83.Google Scholar
Wallage, M. J., and Imrie, C. T. 1997. ‘Supramolecular dimeric liquid crystals. The liquid crystalline behaviour of mixtures ofα-(4-pyridyloxy)-ω -[4-(4-butylphenylazo)phenoxy]alkanes and 4-octyloxybenzoic acid’. J Mater Chem 7:1163–7.Google Scholar
Humphries, R. L., James, P. G., and Luckhurst, G. R. 1971. ‘A molecular field treatment of liquid crystalline mixtures’. Symp Faraday Soc 5:107–18.Google Scholar
Humphries, R. L., and Luckhurst, G. R. 1973. ‘A statistical theory of liquid crystalline mixtures. Components of different size’. Chem Phys Lett 23:567–70.Google Scholar
Attard, G. S., and Imrie, C. T. 1992. ‘Liquidcrystalline and glass-forming dimers derived from 1-aminopyrene’. Liq Cryst 11:785–9.Google Scholar
Goodby, J. W. 1991. ‘Chirality in liquid crystals’. J Mater Chem 1:307–18.Google Scholar
Shiraishi, K., Kato, K., and Sugiyama, K. 1990. ‘Synthesis and electrooptical properties of terminal–terminal type of ferroelectric liquid crystal’. Chem Lett 971–4.Google Scholar
Barbera, J., Omenat, A., and Serrano, J. L. 1989. ‘New chiral smectic liquid crystals with the assymetrical carbon in the central part of the molecule’. Mol Cryst Liq Cryst 166:167–71.Google Scholar
Barbera, J., Omenat, A., Serrano, J. L., and Sierra, T. 1989. ‘New dimeric liquid crystals with chiral flexible spacers’. Liq Cryst 5:1775–82.Google Scholar
Yoshizawa, A., Matsuzawa, K., and Nishiyama, I. 1995. ‘Coupling between chirality and odd–even effect of twin materials in smectic liquidcrystalline phases’. J Mater Chem 5:2131–7.Google Scholar
Suzuki, Y., Isozaki, T. Kusumoto, T., and Hiyama, T. 1995. ‘Synthesis and properties of dimeric antiferroelectric liquid crystals’. Chem Lett 8:719–20.Google Scholar
Yoshizawa, A., Soeda, Y., and Nishiyama, I. 1995. ‘Liquid-crystalline properties of a chiral twin material possessing a remarkably flexible central spacer’. J Mater Chem 5:675–81.Google Scholar
Yoshizawa, A., and Nishiyama, I. 1995. ‘Interlayer correlation in smectic phases induced by chiral twin molecules’. Mol Cryst Liq Cryst 260:403–22.Google Scholar
Suzuki, Y. I., Isozaki, T., Hashimoto, S.,et al. 1996. ‘A stability of the antiferroelectric phase in dimeric liquid crystals having two chiral centres with CF3 or CH3 groups; evaluation of conformational and electric interactions’. J Mater Chem 6:753–60.Google Scholar
Marcelis, A.T. M., Koudijs, A., and SudhoÈlterr, E. J. R. 1996. ‘Thermal and optical properties of chiral twin liquid crystalline bis (cholesteryl) alkanedioates’. J Mater Chem 6:1469–72.Google Scholar
Faye, V, Babeau, A., Placin, F., Nguyen, H. T., Barois, P., Laux, V., and Isaert, N. 1996. ‘SC* A and S [Ctilde]* phases in chiral non-symmetric dimesogens’. Liq Cryst 21:485–503.Google Scholar
Marcos, M., Omenat, A., and Serrano, J. L. 1993. ‘Novel ferroelectric non-symmetric dimeric liquid crystals’. Liq Cryst 13:843–50.Google Scholar
Marcelis, A. T. M., Koudijs, A., and SudhoÈlterr, E. J. R. 1994. ‘Odd–even effects in the optical properties of chiral twin liquid-crystalline cholesteryl ω-(cyanobiphenylyloxy) alkanoates’. Recl Trav Chim Pays-Bas 113:524–6.Google Scholar
Marcelis, A. T. M., Koudijs, A., and SudhoÈlterr, E. J. R. 1995. ‘Odd–even effects in the thermotropic and optical properties of three series of chiral twin liquid crystals’. Liq Cryst 18:843–50.Google Scholar
Hardouin, F., Achard, M. F., Jin, J.-I., and Yun, Y. K. 1995. ‘From incommensurability to commensurability in smectic phases for a series of dimesogenic liquid crystals’. J Phys II Fr 5:927–35.Google Scholar
Hardouin, F., Achard, M. F., Jin, J. I., Shin, J. W., and Yun, Y. K. 1994. ‘Novel sequence with incommensurate SA phases in a new dimesogenic liquid crystal’. J Phys II Fr 4:627–43.Google Scholar
Nishiyama, I., Ishizuka, H., and Yoshizawa, A. 1993. ‘Strong helical structures produced by dimeric liquid crystals possessing the chiral centre in the central region of the molecular structure’. Ferroelectrics 147:193–204.Google Scholar
Pelzl, G., Humke, A., Diele, y, Demus, D., and Weissflog, W. 1990. ‘Filled smectic A phases in binary liquid-crystalline systems of terminal-nonpolar compounds’. Liq Cryst 7:115–22.Google Scholar
Luckhurst, G. R., Stephens, R. A., and Phippen, R. W. 1990. ‘Computer simulation studies of anisotropic systems. XIX. Mesophases formed by the Gay–Berne model mesogen’. Liq Cryst 8:451–64.Google Scholar
Brownsey, G. J., and Leadbetter, A. J. 1981. ‘Novel liquid crystal structures in cyano bi-cyclohexanes’. J Phys Lett, Paris 42:135–9.Google Scholar
Irvine, P. A., Wu, D. C., and Flory, P. J. 1984. ‘Liquidcrystalline transitions in homologous p-phenylenes and their mixtures. Part 1.—Experimental results’. J Chem Soc, Faraday Trans 1 80:1795–806.Google Scholar
Jin, J. I., Chung, B. Y., and Park, J. H. 1991. ‘Dimesogenic compounds consisting of two identical terminal N-(4-oxybenzylidene)-4-nbutylaniline units and a central polymethylene spacer’. Bull Korean Chem Soc 12:583–7.Google Scholar
Rozhanskii, I. L., Tomita, I., and Endo, T. 1996. ‘Synthesis and thermal properties of dimeric alkoxy-substituted tolans’. Liq Cryst 21:631–43.Google Scholar
Jin, J. I., Oh, H. T., and Park, J. H. 1986. ‘Thermotropic compounds having two terminal mesogenic units and central spacers. Part 7. Homologous α,ω-bis-[p-(4-alkoxyphenoxycarbonyl) phenoxy]alkanes’. J Chem Soc Perkin Trans 2:343–7.Google Scholar
Griffin, A. C., Buckley, N. W., Hughes, W. E., and Wertz, D. L. 1981.‘Effect of molecular structure on mesomorphism.11. 1 A Siamese twin liquid crystal having two independently smectogenic conformations’. Mol Cryst Liq Cryst 64:139–44.Google Scholar
Griffin, A. C., Thames, S. F., and Bonne, M. S. 1976. ‘Effect of molecular structure on mesomorphism. Two series of novel methylene-bridged’. Liq Cryst 34:135–9.Google Scholar
Dehne, H., Roger, A., Demus, D., Diele, S., Kresse, H., Pelzl, G., Wedler, W., and Weissflog, W. 1989. ‘Sulphur ligated siamese twin mesogens’. Liq Cryst 6:47–62.Google Scholar
Weissflog, W., Demus, D., Diele, S., Nitschke, P., and Wedler, W. 1989. ‘From laterally branched mesogens to novel twin molecules’. Liq Cryst 5:111–22.Google Scholar
Huh, S. M., Jin, J. I., Achard, M. F., and Hardouin, F. 1998. ‘H-shaped dimeric LC compounds: Synthesis and thermotropic properties of alpha, omega-bis\ [2,5-bis(4-ethoxyphenoxycarbonyl)phenoxy] alkanes’. Liq Cryst 25:285–93.Google Scholar
Huh, S. M., Jin, J. I., Achard, M. F., and Hardouin, F. 1999. ‘Synthesis and liquid crystalline properties of new H-shaped twin compounds: A series of 1,6-bis [2,5-bis(4 alkoxyphenoxycarbonyl)phenoxy] hexanes’. Liq Cryst 26:919–24.Google Scholar
Lub, J., Broer, D. J., and Allan, J. F. 1999. ‘The synthesis and polymerisation of a liquid crystalline crosslinkable thiol-ene molecule’. Mol Cryst Liq Cryst 332:259–66.Google Scholar
Andersch, J., and Tschierske, C. 1996. ‘Synthesis and liquid crystalline properties of novel laterally connected twins’. Liq Cryst 21:51–63.Google Scholar
Kumar, B., Prajapati, A. K., Varia, M. C., and Suresh, K. A. 2009. ‘Novel mesogenic azobenzene dimer at air–water and air–solid interfaces’. Langmuir 25:839–44.Google Scholar
Prajapati, A. K., Varia, M. C., and Sahoo, S. P. 2011. ‘H-shaped mesogenic dimers containing polar – NO2 –Cl terminus’. Liq Cryst 38:861–9.Google Scholar
Prajapati, A. K., Varia, M. C., and Sahoo, S. P. 2011. ‘Azoester-based H-shaped symmetrical mesogenic dimers containing –CH3 –OCH3 terminal substituent’. Phase Transit 84:325–42.Google Scholar
Varia, M. C., Kumar, S., and Prajapati, A. K. 2012. ‘H-shaped azoester oxymethylene containing twin liquid crystalline compounds’. Liq Cryst 39:365–71.Google Scholar
Prajapati, A. K., and Varia, M. C. 2013. ‘H-shaped symmetrical twin liquid crystalline compounds with polar-terminal substituents’. Liq Cryst 40:1151–8.Google Scholar
Ishizuka, H., Nishiyama, I., and Yoshizawa, A. 1995. ‘Helical structures induced by laterally-connected chiral twin molecules’. Liq Cryst 18:775–9.Google Scholar
Weissflog, W., Demuss, D., and Dieles, S. 1990. ‘From laterally branched mesogens to novel twin molecules. Part II Mol Cryst Liq Cryst 191:9–15.Google Scholar
Lee, J. W., Piao, X. L., Yun, Y. K., and Jin, J. I. 1999. ‘Synthesis and liquid crystalline properties of T-shaped dimesogenic compounds’. Liq Cryst 26:1671–85.Google Scholar
Bae, W. S., Lee, J. W., and Jin, J. I. 2001. ‘Comparison of liquid crystalline properties of dimeric compounds of different skeletal shapes’. Liq Cryst 28:59–67.Google Scholar
Varia, M. C., Kumar, S., and Prajapati, A. K. 2012. ‘T-shaped non-symmetrical twin liquid crystalline compounds’. Liq Cryst 39:933–42.Google Scholar
Yoshizawa, A., Sato, M., and Rokunohe, J. 2005. ‘A blue phase observed for a novel chiral compound possessing molecular biaxiality’. J Mater Chem 15:3285–90.Google Scholar
Vorlander, D., and Apel, A. 1932. ‘Die Richtung der Kohlenstoff-Valenzen in Benzolabkömmlingen (II.)’. Chem Ber 65:1101–9.Google Scholar
Kuboshita, M., Matsunaga, Y., and Matsuzaki, H. 1991. ‘Mesomorphic behavior of 1,2-phenylene bis[4-(4-alkoxybenzylideneamino)benzoates’. Mol Cryst Liq Cryst 199:319–26.Google Scholar
Matsunaga, Y., and Matsuzaki, H. 1993. ‘New mesogenic compounds with unconventional molecula r st r uctures 1,2-phenylene and 2,3-naphthylene bis[4-(4 alkoxyphenyliminomethyl) benzoates] and related compounds’. Liq Cryst 14:105–20.Google Scholar
Kato, T., Adachi, H., Fujishima, A., and Fre'chet, J. M. J. 1992. ‘Self-assembly of liquid crystalline complexes having angular structures through intermolecular hydrogen bonding’. Chem Lett 21:265–8.Google Scholar
Attard, G. S., and Douglass, A. G. 1997. ‘U-shaped dimeric liquid crystals derived from phthalic acid’. Liq Cryst 22:349–58.Google Scholar
Yamaguchi, A., Watanabe, M., and Yoshizawa, A. 2007. ‘Odd–even effects in the phase transition behaviour of novel U-shaped liquid crystals’. Liq Cryst 34:633–9.Google Scholar
Rahman, M. L., Biswas, T. K., Sarkar, S. M., Yusoff, M. M., Malek, M. N. F. A., and Tschierske, C. 2015. ‘New U-shaped liquid crystals azobenzene derived from catechol for photoswitching properties’. J Mol Liq 202:125–33.Google Scholar
Rokunohe, J., Yamaguchi, A., and Yoshizawa, A. 2005. ‘Physical properties of a novel chiral material possessing a binaphthyl group’. Liq Cryst 32:207–12.Google Scholar
Rokunohe, J., and Yoshizawa, A. 2005. ‘An unusual phase sequence of iso liq-blue phase-smectic A observed for novel binaphthyl mesogenic derivatives’. J Mater Chem 15:275–9.Google Scholar
Itoh, M., Tokita, M., Adachi, K., Hayakawa, T., Kang, S., Tezuka, Y., and Watanabe, J.Synthesis of macrocyclised dimetric compounds and their liquid crystal transition behaviours’. Liq Cryst 36:1443–50.

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