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Molecular Flexibility Operated Mesomorphism

Wybrane pełne teksty z tego czasopisma
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Novel homologous series: RO-CNsub>6H4-CH=CH-COO-CH2-C6H4-Br (p) synthesized and studied with a view to understand and establish the effects of molecular structure on liquid crystal (LC) behavior of a series. Series consists of eleven homologues. C1 to C7 members of a novel series are non-liquid crystals. Mesomorphism commences from Octyloxy (C8) homologue and continued upto hexadecyloxy homologue (C16) as enantiotropic nematic without exhibition of smectic property. The textures of a nematic phase are threaded or Schlieren. Transition temperatures (table-2) and textures are determined by an optical polarizing microscopy equipped with a heating stage. Cr-N/I and N-I transition curve behaved in normal manner in phase diagram, showing their phase behavior (figure-1). Odd-even effect is absent for N-I transition curve. Analytical and spectral data confirmed the molecular structures of a series. The LC properties are compared with the structurally similar series. The transition temperatures are relatively lower than the corresponding n-alkoxy benzoic acid. Thus, present novel series is partly nematogenic with absence of smectic property whose mesogenic phase length is low and of low ordered melting type. Thermal stability for nematic is 93.0°C and the mesophaselength ranges from 8 to 21°C. Keywords : Mesomorphism; Nematic; enantiotropy; Liquid Crystal; Smectic
Słowa kluczowe
Rocznik
Tom
Strony
163--171
Opis fizyczny
Bibliogr. 30 poz., rys., tab., wz.
Twórcy
  • Huntsman International India Pvt. Ltd, Umraya village, Taluka: Padra, Vadodara-391 440, Gujarat, India, Dr. K.N. Modi University, Newai, Dist. Tonk, Rajasthan-304021
autor
  • P.T. Arts and Science College, Godhara
autor
  • Dr. K.N. Modi University, Newai, Dist. Tonk, Rajasthan-304021
Bibliografia
  • [1] F. Reinitzer, Monatsh 9, 421 (1888)
  • [2] Naemura, S. (2001). Advance LCD technologies, Displays, 22 (1), 1.
  • [3] W.S. Kim, Elston, S.J., & Raynes, F.P. (2008). Display, 29, 458-463.
  • [4] ImaranTadwee, Dr. Sahanashahi, Vivek Ramteke, Iftequar Syed, Liquid Crystals pharmaceutical Application: A review, IJPRAS, ISSN 2277-36. Vol. 1, Issue 2 (2012), 06-11.
  • [5] E.Hertz, B.Lavorel and O.Faucher, Optical imagin by molecular gas, Nature photon; 5 (2011) PP. 783.
  • [6] G.W. Gray and P.A. Winsor (Eds) Liquid Crystals and plastic crystals, chapter-6.2, The role of liquid crystal in life processes by G.T. Stewart, Vol-1, PP. 308-326.
  • [7] G. Rajesh, K. Mansi, K. Srikant, B. Babasaheb, D. Nagesh, S.Kavita, C. Ajay, Chem. Pharm. Bull, 2008, 56, PP. 897-901.
  • [8] Prajkata P.Gaikwad, Maya T.Desai, “ Liquid crystalline phase and its Pharma application’’ International journal of Pharma Research and Review , Dec.2013; 2 (12) : 40-52.
  • [9] G.W. Gray (1974) In; G.W. Gray and P.A Winsor (eds) liquid crystals and plastic crystals, Chapter-4, Volume-1, PP-103-153.
  • [10] G. W. Gray, Molecular structures and properties of liquid crystals, Academic press, Landon, 1962.
  • [11] G.W. Gray and B. Jones, Mesomorphism and chemical constitution part-3, The effect of halogen substitution on the 4-Alkoxy benzoic acids. Journal of chemical society (1954), PP. 2556-2562.
  • [12] C. T. Imrie, Liq. Crystal dimers. Struct. Bond 95 (1999) PP. 149-192.
  • [13] D.Demus, 100 years of liquid crystal chemistry, mol.cryst. liq.cryst. 165 (1988) PP.45-84.
  • [14] D. Demus, Plenary lectures 100 years of liquid crystals chemistry, Thermotropic liquid crystals with conventional and unconventional molecular structures, Liq.Cryst, 5 (1988). PP. 75-110
  • [15] D. Demus, Plenary lectures 100 years of liquid crystals chemistry, Thermotropic liquid crystals with conventional and unconventional molecular structures, Liq.Cryst, 5 (1988). PP. 75-110
  • [16] Doshi et al (i) D.M. Suthar and A.V. Doshi, Mol. Cryst. Liq. Cryst. Vol. 575, PP. 76-83. (ii) H. N. Chauhan and A. V. Doshi, Mol. Cryst. Liq. Cryst. Vol. 570, PP. 92-100 (2013) (iii) R.P. Chaudhari, M.L. Chauhan and A.V Doshi, Vol. 575, PP. 88-95 (2013) (iv) U.C. Bhoya, N.N. Vyas and A.V. Doshi, Mol. Cryst. Liq. Cryst. Vol. 552. PP. 104-110. (2012).
  • [17] D. M. Suthar, A.A. Doshi and A.V. Doshi “ Study of liquid crystalline state and evaluation of its properties through a novel homologous series’’, Mole. Cryst. Liq. Vol.582, PP.79-87, 2013.
  • [18] Upendra K. Jain, Rich K Bhatia, Akkinepally R. Rao, Ranjit Singh, Ajit K. Saxena and Irun Seha “ Design and Development of halogenated Chalcone derivatives as potential cancer Agents” Tropical Journal of pharmaceutical Research, January 2014: 13 (1), 73-80.
  • [19] B.H. Patel and Doshi A.V (2015) ‘ Novel Cinnamate ester-Synthesis and Mesomorphic properties in relation to molecular structure’ Molecular Crystal and Liquid crystals, 605, 42- 51. 170 Volume 52
  • [20] Patel .B.H and Doshi A.V. “ Synthesis and Mesomorphic Properties of a Novel Ester Homologous series: 4-(4’-n-Alkoxy Benzoyloxy) benzyl Cinnamates” Mol. Cryst. Liq. Cryst., Vol-606, PP.56-65. (2015)
  • [21] Patel B.H and Doshi A.V. “Dependence of Molecular Structure on Mesomorphic Behaviour with special Reference to Central Bridge” Mol. Cryst. and Liq. Cryst. Vol-608, PP. 38-46. (2015)
  • [22] Hird. M, Toyne. K. J, and Gray. G. W, Day S.E and Mc. Donell D.G (1993), Liq. Cryst. 15, PP.123.
  • [23] P.J. Collings and M. Hird (1997), Introduction of Liquid crystals chemistry and physics, Taylor and Francis Ltd. U.K. 1998.
  • [24] Marcos. M, Omenat. A, Serrano. J.L and Ezcurra. A (1992), Adv. Matter, 4, 285
  • [25] Hird. M, Toyne. K.J, Gray G.W., Day S.E. (1993) Liq. Cryst. 14, PP. 741.
  • [26] (a) Pieter-Ooms, Krefeld, Bernd-Ulrich Schenke, Bottrop, ‘ Process for the preparation of Hydroxybenzoic benzyl esters’ United states of patent no: 2003/0053964 A1, Mar. 20, 2003. (b) European Patent EP0117502B1, Process of producing benzyl ester of aromatic hydrocarboxylic acid (Example-1), page 4, date of Publica. 19-11-1987.
  • [27] Rajesh.B. Marathe and Doshi A.V, Manuscript of a research paper entitled “Mesomorphism Dependance on Terminally Substituted End groups” accepted for publication to Mol. Crystal Liq. Crystal journal (Taylor and Francis) with its LCMH No.281, dated. 03.08.2014.
  • [28] Brijesh H. Patel and A.V Doshi, “Synthesis and liquid crystal properties of novel homologous series: 4-(4’-n-alkoxybenzyloxy) Benzyl benzoates’ ‘Molecular Crystals and Liquid crystals’, 605:1, 61-69, 15.12.2015.
  • [29] Patel, B.H. and Doshi, A. V. (2015). Mol Cryst. Liq. Cryst., 607, 78-86
  • [30] Rajesh.B. Marathe and Doshi A.V, Manuscript of a research paper entitled “Mesomorphism Dependance on Molecular Rigidity with Reference to –CH=CH- Unit of Central Bridge” accepted for publication to Mol. Crystal Liq. Crystal journal (Taylor and Francis) with its LCMH No.315.
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-4c11e396-5168-4d01-8a93-20ee92ff17f8
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