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Tytuł artykułu

Dependence of Mesomorphism on Molecular Rigidity

Wybrane pełne teksty z tego czasopisma
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A novel smectogenic homologous series of twelve homologues synthesized and studied with a view to understand and establish the effect of molecular structure on liquid crystal properties (LC) and LC behaviors of thermotropic homologues. First (C1) to last (C16) member of a series exhibited only enantiotropically smectogenic property without showing nematic property which is absent even in the monotropic condition. Transition and melting temperature including textures of homologues were determined by an optical polarizing microscopy equipped with a heating stage, texture of a smectic phase are of the type A or C. Smectogenic phase length ranger between 5.1oC to 22.6oC. SmecticIsotropic (Sm-I) thermal stability is 153.55oC. Analytical, spectral and thermal data supported molecular structures of homologues. LC behaviors of present novel series are compared with the structurally similar homologous series. Transition curves viz. Cr-Sm and Sm-I transition curves of a phase diagram behaved in normal manner.
Słowa kluczowe
Rocznik
Tom
Strony
67--76
Opis fizyczny
Bibliogr. 23 poz., rys., wykr., wz.
Twórcy
autor
  • Department of Chemistry, Saurashtra University, Rajkot - 360005, Gujarat, India
autor
  • Department of Chemistry, Saurashtra University, Rajkot - 360005, Gujarat, India
autor
  • Department of Chemistry, Saurashtra University, Rajkot - 360005, Gujarat, India
Bibliografia
  • [1] Reinitzer, F., Monatsh (1888). 9, 421.
  • [2] Naemura, S. (2001). Advance LCD technologies, Displays, 22 (1), 1.
  • [3] Talwa, I., Dr.Salnana Shahi, Ramteke,V. & Syed, I. (2012). “Liquid crystal Pharmaceutical Application: A Review”, “IJPRAS” International journal of Pharmaceutical Research and Allied Science, 1(2), 06-11.
  • [4] Hertz, E., Laorel, B., &Faucher,O. (2011). Nature photon, 5, 78-79.
  • [5] Calliste, C.A., Bail, J.C., Trouilas, P., Pouget, C., Chulia.A.J. & Duroux, L.J. (2001). Anticancer Res., 21, 3949-3956.
  • [6] Gray, G. W., & Windsor, P. A. (1974). Liq.Cryst. and Plastic Cryst., The role of liquid crystals in life processes by Stewart G.T., 1, 308-326.
  • [7] Gray, G. W. (1962). Molecular Structure and the Properties of Liquid Crystal. Academic Press: London.
  • [8] Gray, G. W., & Windsor, P.A. (1974). Liq. Cryst. Plastic Cryst., Ellis Horwood: Chichester, U.K., 1 (4), 103-153.
  • [9] Gray, G.W. & Jones, B. (1954).Mesomorphism and Chemical Constitution part-III.4- alkoxy benzoic acid, J. of Chem. Soc., pp.2556-2562.
  • [10] Imrie, C.T. (1999). Liquid crystal dimers, Structure, Bond, 95,149-192.
  • [11] Demls, D. (1988). 100 years of Liquid Crystal Chemistry, Mol. Cryst. Liq. Cry., 165, pp. 45-84.
  • [12] Demus, D. (1989). Plenary lectures 100 years of Liquid Crystal Chemistry, Thermotropic liquid crystals with conventional and unconventional molecular structure, Liq. Cry., 5, pp. 75-110.
  • [13] Imrie, C.T. & Luckhrust, G.R. (1998). Liquid Crystal dimers and oligomers: Handbook of liquid crystal, law molecular liquid crystals, 2B, Demus,D., Goodly, J.W., Spiess, H.W. and Vill,V.,willey-VCH, weinhei, 801 833.
  • [14] Vora, R.A., Prajapati, A.K., Kevat, J.B. & Raina, K.K. (2001).Mesogenic properties and the effect of 1,2,4 trisubstitution on the central benzene nucleus of a three ring mesogens. Liq.cryst.28, 983-989.
  • [15] Hird, M., Toyne, K. J., Gray, G. W., Day, S. E., & Mc Donnell, D. G. (1993). Liq. Cryst., 15, 123.
  • [16] Collings, P.J. & Hird, M., (1998). Introduction to liquid crystals chemistry and physics, Taylor and Francis, U.K.
  • [17] Marcos, M., Omenat, A., Serrano, J. L., & Ezcurra, A. (1992). Adv. Mater., 4, 285.
  • [18] Hird, M., Toyne, K. J., & Gray, G. W. (1993). Liq. Cryst., 14, 741.
  • [19] Dave, J. S., & Vora, R. A., (1970). Liquid Crystal and Ordered Fluids, Plenum Press: New York, Graw, G. W. (1958). Steric effect in conjugated systems. Ed., Butterworths, London, 477.
  • [20] Patel, R. B., Patel, V. R., & Doshi, A. V. (2012). Mol. Cryst. Liq. Cryst., 552, 3-9.
  • [21] Nagaveni, N.G., & Prasad, V., (2013). “Azo substituted V-shaped liquid crystalline compounds: synthesis and mesophase characterization”, Phase Tran. 86, 12, 1227- 1240.
  • [22] Dave, J.S., Upasani, C.B., & Patel, P.D. (2010). Mol.Cryst.Liq.Cryst., 73, 533.
  • [23] Chauhan, H.N., & Doshi., A.V. (2013). Mol.Cryst.Liq.Cryst., 575(1), 96-103.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-507c0962-bb6e-4841-bf65-fa2b828ef4af
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