This work is licensed under a
Creative Commons Attribution 4.0 International License
[1] F. Reinitzer, Monatsh 9, 421, (1888).
[2] W.S. Kim, S.J. Elston, and F.P. Raynes, Display29 (2008) PP. 458-463.
[3] S. Narmura. Advance LCD technologies, Displays 22 (1) (2001) PP.
[4] G.W. Gray and P.A. Winster (Eds) Liquid Crystal and plastic crystals, chapter-6. 2, The role of liquid crystal in life processes by G.T. Stewart, Vol-1, PP. 308-326.
[5] C.A. Calliste, J. Cle Bail, P. Trouilas, C Poug, A.J. Chulia, L.J. Durous, Anticancer, Res. 2001, 21, 3949-3956.
[6] Y. Jahng, L. Zhao, Y. Moon, A. Basnet, E. Kim, H.W. Chang, H.K. Ju, T.C. Jeong, E.S. Lee, Bio-Org, Med. Chem. Lett. 2004, 14, 2559-2562.
[7] Upendra K Jain , Rich K Bhatia, Akkinepally R. Rao, Ranjit singh , Saxsena Ajit K and Seha lrun Design and Development of Halogenated Chalcone derivatives as potential anticancer Agents , Tropical Journal of pharmaceutical Research, January 2014: 13(1), 73-80.
DOI: https://doi.org/10.4314/tjpr.v13i1.11[8] Prajkata P. Gaikwad , Desai Maya T. Liquid crystalline phase and its Pharma application, International journal of Pharma Research and Review, Dec. 2013; 2 (12); 40-52.
[9] E. Hertz, B. Lavorel and O. Faucher , Optical imagine by molecular gas, Nature photon; 5 (2011) PP. 783.
[10] C.T. lmrie, Liq. Crystal dimers. struct. Bond 95 (1999) PP. 149-192.
[11] Gray G.W. (1974) ln; Gray G.W. and P.A. Winsor P.A. (eds) liquid crystal and plastic crystals, Chapter-4 , Volume-1, PP-103-153.
[12] Gray G.W., Molecular Structure and properties of liquid crystals, Academic press, Landon, (1962).
[13] Gray G.W. and Jones B., 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.
DOI: https://doi.org/10.1039/jr9540002556[14] P.A. Henderson, O. Niemeyer, and C.T. Imrie, Methylene-linked liquid crystal dimers, Liq. Cryst. 28 (2001), PP. 463-472.
DOI: https://doi.org/10.1080/02678290010007558[15] Dermus D., Plenary lectures 100 years of liquid crystals chemistry, Thermotropic liquid crystals with conventional and unconventional molecular structures, Liq. Cryst, 5 (1998). PP. 75-100.
DOI: https://doi.org/10.1080/02678298908026353[16] Dermus D., 100 years of liquid crystals chemistry, mol. Cryst. 165 (1998) PP. 45-84.
[17] lmrie C. T and Luckhrust G. R, " Liquid Dimers and Oligomers in handbook of Liquid Crystal, law molecular liquid crystals; Vol. 2B, Demus D. , Goodby J.W., Graw G.W., Spiess H. and Vill V. eds, Willey-VCH weinhe 1998, PP-801-833.
DOI: https://doi.org/10.1002/9783527619276[18] Doshi et al (i) Suthar D.M. and Doshi A.V., Mol. Cryst. Liq. Cryst. Vol. 575, PP. 76-83. (ii) Chauhan H.N. and Doshi A.V., Mol. Cryst. Liq. Cryst. Vol. 570, PP. 92-100 (2013).
[19] Patel B.H. and Doshi A.V. "Novel Cinnamates Esters-Synthesis and Mesomorphic Properties in Relation to Molecular Structure., Mol. Cryst. Liq. Cryst., vol-605, PP. 42-51 (2015).
[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).
DOI: https://doi.org/10.1080/15421406.2014.915627[21] Doshi A.V., Joshi C. G, Patel V.R. Synthesis and Study of Liquid Crystallinity of Benzoates Derivatives in a Laterally substituted Homologous series: n-Propyl-o-[p, -n-alkoxy benzoyloxy] benzoates. Der Pharma Chemica, 3(5): 233-239. (2011).
[22] Doshi A.V., Patel R.B., Study of a new homologous series of Cis Cinnamate ester of Mesogens: n-Hexyl-p-(p, -n-alkoxy cinnamoyloxy) cinnamates. Der Pharma Chemica, 3(1): 338-348. (2011).
[23] Doshi A.V., Patel V.R., Study of Azo ester mesogens: 4-(4'-n-alkoxy benzoyloxy)-3- Methoxy-phenyl azo-4', -Nitrobenzene. Der Pharma Chemica, 2(6): 439-436. (2010).
[24] Doshi A.V., Makwana N.G., Synthesis and Study of a new mesogenic Homologous series: 4-(4'-n-alkoxy benzoyloxy)-3, 5-dichloro phenylazo-4', -methyl benzene., Der Pharma Chemica, 3(2): 433-439. (2011).
[25] Chauhan B.C., Doshi A.V., Synthesis and study of Thermotropic Mesogenic homologous series: p-(p'-n-alkoxy benzoyloxy)-m-chlorophenyl azo-p', - chlorobenzene. Der Pharma Chemica, 3(1): 172-180. (2011).
[26] Bhoya U.C., Doshi A.V., Patel R.B., Study of new homologous series of azoester mesogens: p-(p'-n-alkoxy benzoyloxy)-m-methylphenylazo-p', -methoxybenzene. Der Pharma Chemica, 3(3): 115-123. (2011).
[27] Hird. M, Toyne. K. J, Gray G.W., Day S.E. and Mc. Donell D.G. (1993), Liq. Cryst. 15 PP. 123.
[28] P.J. Collings and M. Hird (1997), Introduction of Liquid crystals chemistry and Physics, Taylor and Francis Ltd. U.K. (1998).
[29] Macros . M, Omenat. A, Serrano. J. L and Ezcurra. A(1992) , Adv. Matter, 4, 285.
[30] Hird. M, Toyne. K. J, Gray G.W., Day S.E. (1993) Liq. Cryst. 14, PP. 741.
[31] Dave J. S and Vora R. A (1970). In: J.F. Johnson and R.S. Porter, (eds), (Liquid Crystals and ordered fluids, Plenum Press: New York, P. 447.
[32] Vogel A.I. Textbook of practical organic chemistry, 5th ed. ELBS and Longmann, London. (1989) 946.
[33] Uhood J.A., international Journal of Molecular Science., vol. 12; PP. 3182-3190 (2011).
[34] ohar J. M and Doshi A.V., Studies on mixed mesomorphism: Determination of latent transition temperature (LTT) by extrapolation, proceeding of Indian Acad. Of Science-Bangalore, Vol-105, N0-3, June 1993, PP. 209-214.
[35] Ganatara K.J. and Doshi A.V., Study of binary systems inducing mesophase and determination of latent Transition Temperature,. Journal of Indian Chem. Soc., Vol. 77, July 2000, PP. 322-325.
[36] Bhoya U.C., Vyas N.N. and Doshi A.V., Mol. Cryst. Liq. Cryst., Vol. 552. PP. 104-110. (2012).
[37] Doshi A.V., Bhoya U.C., Travadi J.J., Mol. Cryst. Liq. Cryst., Vol. 552. PP. 10-15, (2012).
[38] Vinay S. Sharma, Ravindra B. Solanki and R.B. Patel , Manuscript of the research paper entitled, Molecular Structure and Mesomorphism: Effect of Tail/Lateral Group, submitted for publication in Mol. Cryst. Liq. Cryst. Journal with its reference no. LCMH No. 326 date 28th April (2015).
[39] Doshi A.V., Chaudhari R.P., Mol. Cryst. Liq. Cryst., vol. 570, PP. 109-116, (2013).
[1] V. Sharma, R. Patel, "Tuning the mesomorphic properties of nonisomeric chalconyl-ester bases homologous series: The effect of tail group", Molecular Crystals and Liquid Crystals, Vol. 643, p. 40, 2017
DOI: https://doi.org/10.1080/15421406.2016.1262686[2] V. Sharma, R. Patel, "Effect of alkyl chain in the terminal ester group on mesomorphic properties of new rod like homologous series: Synthesis and characterization", Molecular Crystals and Liquid Crystals, Vol. 643, p. 62, 2017
DOI: https://doi.org/10.1080/15421406.2016.1262690[3] P. Patel, R. Shah, "Dependence of mesomorphism on geometrical shapes of isomeric and nonisomeric series of chalconyl esters", Molecular Crystals and Liquid Crystals, Vol. 643, p. 168, 2017
DOI: https://doi.org/10.1080/15421406.2016.1264227[4] V. Sharma, R. Patel, "Synthesis, characterization, and mesomorphic investigation of vinyl ester-substituted chalcones and effect of lateral ‒NO2 and ‒OCH3 group", Molecular Crystals and Liquid Crystals, Vol. 643, p. 241, 2017
DOI: https://doi.org/10.1080/15421406.2016.1272814[5] V. Sharma, R. Vekariya, A. Sharma, R. Patel, "Mesomorphic properties of liquid crystalline compounds with chalconyl central linkage in two phenyl rings", Liquid Crystals Today, Vol. 26, p. 46, 2017
DOI: https://doi.org/10.1080/1358314X.2017.1359401