References
- Kobzar Y, Tkachenko I, Shekera O, et al. The fluorine-containing polyazomethines: synthesis and properties. Polym. J. 2014;36:331–340.
- Pron A, Rannou P. Processible conjugated polymers: from organic semiconductors to organic metals and superconductors. Prog. Polym. Sci. 2002;27:135–190.
- Grigoras M, Catanescu CO. Imine oligomers and polymers. J. Macromol. Sci. Part C Polym. Rev. 2004;44:131–173.
- Iwan A, Sek D. Processible polyazomethines and polyketanils: from aerospace to light-emitting diodes and other advanced applications. Prog. Polym. Sci. 2008;33:289–345.
- Kumar S, Dhar DN, Saxena P. Applications of metal complexes of Schiff bases – a review. J. Sci. Ind. Res. 2009;68:181–187.
- Hussein MA, Abdel-Rahman MA, Asiri AM, et al. Review on: liquid crystalline polyazomethines polymers. Basics, syntheses and characterization. Des. Monomers Polym. 2012;15:431–463.
- Zhang W, Wang C, Liu G, et al. Structural effect on the resistive switching behavior of triphenylamine-based poly(azomethine)s. Chem. Commun. 2014;50:11496–11499.
- Ravikumar L, Kalaivani S, Vidhyadevi T, et al. Synthesis, characterization and metal ion adsorption studies on novel aromatic poly(azomethine amide)s containing thiourea groups. Open J. Polym. Chem. 2014;04:1–11.
- Saegusa Y, Kuriki M, Nakamura S. Preparation and characterization of fluorine-containing aromatic condensation polymers, 4. Preparation and characterization of fluorine-containing aromatic polyazomethines and copolyazomethines from perfluoroisopropylidene group-containing aromatic diamines and/or isopropylidene group-containing aromatic diamines and phthaladehydes. Macromol. Chem. Phys. 1994;195:1877–1889.
- Kumar Gutch P, Banerjee S, Gupta D, et al. Poly‐Schiff bases. V. Synthesis and characterization of novel soluble fluorine‐containing polyether azomethines. J. Polym. Sci., Part A: Polym. Chem. 2001;39:383–388.
- Grimm B, Krüger R-P, Schrader S, et al. Molecular structure investigations on fluorine containing polyazomethines by means of the MALDI–TOF–MS technique. J. Fluorine Chem. 2002;113:85–91.
- Choi E-J, Ahn J-C, Chien L-C, et al. Main chain polymers containing banana-shaped mesogens: synthesis and mesomorphic properties. Macromolecules. 2004;37:71–78.
- K-i Fukukawa, Shibasaki Y, Ueda M. Photosensitive poly (benzoxazole) via poly (o-hydroxy azomethine) II. Environmentally benign process in ethyl lactate. Polym. J. 2004;36:489–494.
- Krebs FC, Jørgensen M. The effect of fluorination in semiconducting polymers of the polyphenyleneimine type. Synth. Met. 2004;142:181–185.
- Ishii J, Tanaka Y, Hasegawa M. Film properties of polyazomethines (2). Poly(imide-azomethine)s derived from ester-containing dialdehydes, tetracarboxylic dianhydrides, and a fluorinated diamine. High Perform. Polym. 2010;22:145–158.
- Cerrada P, Oriol L, Pinol M, et al. Alternative synthetic strategies for Schiff base derived liquid crystal polymers: a comparative study. J. Polym. Sci., Part A: Polym. Chem. 1996;34:2603–2611.
- Stefanache A, Balan M, Harabagiu V, et al. Electro-optical properties of aromatic oligoazomethine/permethylated α-cyclodextrin main-chain polyrotaxanes. Chem. Phys. Lett. 2014;599:104–109.
- Tamareselvy K, Venkatarao K, Kothandaraman H. Synthesis and characterization of new halogen-containing poly (azomethine-urethane) s. Die Makromolekulare Chemie. 1990;191:1231–1242.
- Gauderon R, Plummer CJ, Hilborn JG, et al. Poly(arylene ether azomethine)s: synthesis by aldimine-activated nucleophilic aromatic substitution, characterization, and thin films morphological study. Macromolecules. 1998;31:501–507.
- Butt MS, Akhter Z, Zafar-uz-Zaman M, et al. Synthesis and characterization of some Schiff-base-containing polyimides. Colloid Polym. Sci. 2008;286:1455–1461.
- Kausar A, Zulfiqar S, Ahmad Z, et al. Novel processable and heat resistant poly(phenylthiourea azomethine imide)s: synthesis and characterization. Polym. Degrad. Stab. 2010;95:1826–1833.
- Gul A, Akhter Z, Siddiq M, et al. Synthesis and physicochemical characterization of poly (azomethine) esters containing aliphatic/aromatic moieties: electrical studies complemented by DFT calculation. J. Appl. Polym. Sci. 2014.
- Abid KK, Al-barody SM. Synthesis, characterisation and liquid crystalline behaviour of some lanthanides complexes containing two azobenzene Schiff base. Liq. Cryst. 2014;1–12.
- Ishikawa H, Toda A, Okada H, et al. Relationship between order parameter and physical constants in fluorinated liquid crystals. Liq. Cryst. 1997;22:743–747.
- Ma H, Jen AK-Y, Dalton LR. Polymer-based optical waveguides: materials, processing, and devices. Adv. Mater. 2002;14:1339–1365.
- Krishnan S, Kwark YJ, Ober CK. Fluorinated polymers: liquid crystalline properties and applications in lithography. Chem. Record. 2004;4:315–330.
- Smith JA, DiStasio RA, Hannah NA, et al. SF 5 -terminated fluorinated Schiff base liquid crystals. J. Phys. Chem. B. 2004;108:19940–19948.
- Shevchenko V, Tkachenko I, Shekera O. Nucleus-fluorinated aromatic polyethers. Polym. Sci. Ser. B. 2010;52:408–430.
- Tkachenko I, Shekera O, Bliznyuk V, et al. Fluorinated allyl-, acetyl-, and bromo-containing hydroxyl-substituted phenyl ethers with a hexafluorobenzene or decafluorobiphenyl central unit. J. Fluorine Chem. 2013;149:36–41.
- Tkachenko I, Shekera O, Shevchenko V. Allyl-containing polyaryl ethers with perfluorinated mono-and biphenylene fragments. Polym. Sci. Ser. B. 2013;55:336–343.
- Shevchenko V, Sidorenko A, Bliznyuk V, et al. Synthesis and properties of hydroxylated core-fluorinated diamines and polyurethanes based on them with azobenzene nonlinear optical chromophores in the backbone. Polymer. 2013;54:6516–6525.
- Kaya İ, Avcı A, Kolcu F, et al. Synthesis, characterization, optical, and electrochemical properties of thermal stable novel poly(azomethine-ether)s. Des. Monomers Polym. 2014;17:481–490.
- Cozan V, Gaspar M, Butuc E, et al. Azomethine sulfone macromers with thermotropic liquid crystalline behavior. Eur. Polym. J. 2001;37:1–8.
- Kannan P, Raja S, Sakthivel P. Synthesis and characterization of thermotropic liquid crystalline poly(azomethine ether)s. Polymer. 2004;45:7895–7902.
- Choi E, Ahn H-K, Lee JK, et al. Liquid crystalline twin epoxy monomers based on azomethine mesogen: synthesis and curing with aromatic diamines. Polymer. 2000;41:7617–7625.
- Iwan A, Palewicz M, Sikora A, et al. Aliphatic–aromatic poly(azomethine)s with ester groups as thermotropic materials for opto(electronic) applications. Synth. Met. 2010;160:1856–1867.
- Teoh MM, Chung T-S, Schiraldi DA, et al. Thin-film polymerization and ‘RIS’ Metropolis Monte Carlo simulation of fluorinated aromatic copoly(ester–amide)s. Polymer. 2005;46:3914–3926.
- Yang C-P, Su Y-Y, Hsu M-Y. Syntheses and properties of fluorinated polyamides and poly(amide imide)s based on 9,9-bis[4-(4-amino-2-trifluromethylphenoxy)phenyl]fluroene, aromatic dicarboxylic acids, and various monotrimellitimides and bistrimellitimides. Colloid Polym. Sci. 2006;284:990–1000.
- Sauer BB, Kampert WG, McLean RS. Thermal and morphological properties of main chain liquid crystalline polymers. Polymer. 2003;44:2721–2738.
- Grell M, Bradley DD, Inbasekaran M, et al. A glass-forming conjugated main-chain liquid crystal polymer for polarized electroluminescence applications. Adv. Mater. 1997;9:798–802.
- Wendorff J, Finkelmann H, Ringsdorf H. Structure and morphology of liquid‐crystalline polymers. J. Polym. Sci. Polym. Symp. Wiley Online Library; 1978. p. 245–261.
- Vroege GJ, Lekkerkerker H. Phase transitions in lyotropic colloidal and polymer liquid crystals. Rep. Prog. Phys. 1992;55:1241.
- Lenz RW. Characterization of thermotropic liquid crystalline polymers. Pure Appl. Chem. 1985;57:977–984.
- Nastishin YA, Liu H, Schneider T, et al. Optical characterization of the nematic lyotropic chromonic liquid crystals: light absorption, birefringence, and scalar order parameter. Phys. Rev. E. 2005;72:041711.
- Kim Y-K, Shiyanovskii SV, Lavrentovich OD. Morphogenesis of defects and tactoids during isotropic–nematic phase transition in self-assembled lyotropic chromonic liquid crystals. J. Phys.: Condens. Matter. 2013;25:404202.
- Hwang J, Li P, Carroll WR, et al. Additivity of substituent effects in aromatic stacking interactions. J. Am. Chem. Soc. 2014;136:14060–14067.