PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników
Tytuł artykułu

Dependence of Liquid Crystalline Behaviors on Molecular Flexibility

Wybrane pełne teksty z tego czasopisma
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
A novel homologous series of thermotropic liquid crystal (LC) has been synthesized with a view to understand and establish the effect of molecular structure on liquid crystal behaviors of a series. The present LC series consist of twelve homologues (C1&enspto C16); whose mesomorphic properties commence from octyloxy (C8) homologue of a series. C8, C10&enspand C12 &enspmembers of a series are monotropic smectic and C14, C16&enspmembers are enantiotropically smectogenic. C1&enspto C7 &ensphomologues are nonmesomorphic. Nematogenic property is totally absent. Transition and melting temperatures are determined by an optical polarizing microscopy equipped with a heating stage. Textures of smectic mesophases are focal conic three or two dimensional networking of the type A or C. Cr-I/Sm and Sm-I or I-Sm transition curves behaved in normal manner. Analytical and spectral data confirms the molecular structures of homologues. Thermal stability of smectogenic mesophase is 100.6 oC and mesomorphic phase length is very short (12.9 oC to 15.3 oC). LC properties of a present novel series are compared with the structurally similar homologous series. Present series is partly smectogenic and partly non mesomorphic with poor degree of mesomorphism and middle ordered melting type without exhibition of nematogenic behavior.
Słowa kluczowe
Rocznik
Tom
Strony
77--86
Opis fizyczny
Bibliogr. 22 poz., rys., tab., 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] Kim,W.S., Elston, S.J., & Raynes, F.P. (2008). Display, 29, 458-463.
  • [4] 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.
  • [5] Lee, Y.S., Lim, S.S., Shin, K.H., Kim, Y.S., Ohuchi, K. & Jung, S.H. (2006). Bio.Pharm.Bull, 29, 1028-1031.
  • [6] Imrie, C.T. (1999). Liquid crystal dimers, Structure, Bond, 95,149-192.
  • [7] Gray, G. W., & Windsor, P.A. (1974). Liq. Cryst. Plastic Cryst., Ellis Horwood: Chichester, U.K., 1 (4), 103-153.
  • [8] Gray, G. W. (1962). Molecular Structure and the Properties of Liquid Crystal., Academic Press: London.
  • [9] Demls, D. (1988). 100 years of Liquid Crystal Chemistry, Mol. Cryst. Liq. Cry., 165, 45 84.
  • [10] Demus, D. (1989). Plenary lectures 100 years of Liquid Crystal Chemistry, Thermotropic liquid crystals with conventional and unconventional molecular structure, Liq. Cry., 5, 75- 110.
  • [11] 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.
  • [12] (i) Suthar, D.M., & Doshi, A.V., (2013). Mol.Cryst. Liq.Cryst., 575, 76-83. (ii) Chuhan, H. N., & Doshi, A. V. (2013). Mol. Cryst. Liq. Cry., 570(1), 92-110. (iii) Chaudhari, R. P.,Chauhan, M.L. & Doshi, A.V., (2013). Mol. Cryst. Liq. Cryst., 575, 88-95. (iv) Bhoya, U. C., Vyas, N. N., & Doshi, A. V. (2012). Mol. Cryst. Liq. Cryst., 552, 104-110.
  • [13] Gray, G.W. & Jones, B. (1954). “The effect of halogen substitution on the 4-alkoxy benzoil acid”, Mesomorphism and chemical constitution part-III, J. of Chem. Soc., 2556 2562.
  • [14] Hird, M., Toyne, K. J., Gray, G. W., Day, S. E., & Mc Donnell, D. G. (1993). Liq. Cryst., 15, 123.
  • [15] Collings, P.J., & Hird, M. (1998). “Introduction to liquid crystals chemistry and physics”, Taylor and Fransis Ltd, U.K.
  • [16] Marcos, M., Omenat, A., Serrano, J. L. & Ezcurra, A. (1992). Adv. Mater., 4, 285.
  • [17] Hird, M., Toyne, K. J., & Gray, G. W. (1993). Liq. Cryst., 14, 741.
  • [18] 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.
  • [19] Dave, J. S., & Vora, R. A., (1970). In: J.F. Johnson and R.S. Porter, (Eds), Liquid Crystal and Ordered Fluids, Plenum Press: New York, 477.
  • [20] Nagaveni, N.G., & Prasad, V., (2013). “Azo substituted V-shaped liquid crystalline compounds: synthesis and mesophase characterization”, Phase Tran. 86, 12, 1227-1240.
  • [21] Chauhan, H. N., Vyas,N. N., & Doshi, A. V., (2013) Mol. Cryst. Liq. Cryst., 575, 96 103.
  • [22] Chauhan, M. L., & Doshi, A. V. (2007). J. Ind. Chem. Soc., 84, 774-776.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-d33274e4-701f-4602-abea-8ff4c15872e6
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.