Synthesis and mesomorphic behaviour of unsymmetrical tetracatenar [1,2,3]-triazole derivatives

References

• Zhang B-Y, Jia Y-G, Yao D-S, et al. Preparation and properties of siloxane liquid crystalline elastomers with a mesogenic crosslinking agent. Liq Cryst. 2004;31:339–345. DOI:10.1080/02678290410001648697.
   Web of Science ®Google Scholar
• Colling PJ, Hird M. Introduction to liquid crystals: chemistry and physics. Bristol: Taylor & Francis; 1998.
   Google Scholar
• Wu L-H, Wang Y-C, Hsu C-S. Synthesis and characterization of thiophene-containing liquid crystals. Liq Cryst. 2000;27:1503–1513. DOI:10.1080/026782900750018672.
   Web of Science ®Google Scholar
• Han J, Wang J-Y, Zhang F-Y, et al. Synthesis and mesomorphic behaviour of heterocycle-based liquid crystals containing 1,3,4-oxadiazole/thiadiazole and thiophene units. Liq Cryst. 2008;35:1205–1214. DOI:10.1080/02678290802444129.
   Web of Science ®Google Scholar
• Krivopalov VP, Shkurko OP. 1,2,3-Triazole and its derivatives. Development of methods for the formation of the triazole ring. Russ Chem Rev. 2005;74:339–379. DOI:10.1070/RC2005v074n04ABEH000893.
   Google Scholar
• Yeap G-Y, Alshargabi A, Mahmood WAK, et al. Synthesis, characterization and molecular organization for induced smectic phase of triazole ring in non-symmetric liquid crystalline dimer. Tetrahedron. 2015;71:3939–3945. DOI:10.1016/j.tet.2015.04.036.
   Web of Science ®Google Scholar
• Heng B-T, Yeap G-Y, Mahmood WAK, et al. Alkyl chain self ordering, induction and suppression of mesophase by Cu(II) containing [1,2,3]-triazole-based bidentate salicylaldimine ligands: synthesis, characterisation and X-ray diffraction studies. Liq Cryst. 2014;41:1897–1910. DOI:10.1080/02678292.2014.960488.
   Web of Science ®Google Scholar
• Beltrán E, Robles-Hernández B, Sebastián N, et al. Bent-core luminescent and electroactive bis(triazolyl)triazines with compact columnar mesomorphism. RSC Adv. 2014;4:23554–23561. DOI:10.1039/c4ra02926g.
   Web of Science ®Google Scholar
• Phillips OA, Udo EE, Abdelhamid ME, et al. Synthesis and antibacterial activity of novel 5-(4methyl-1H-1,2,3-triazole)methyloxazolidinones. Eur J Med Chem. 2009;44:3217–3227. DOI:10.1016/j.ejmech.2009.03.024.
   PubMed Web of Science ®Google Scholar
• Kim MK, Kwon J, Kwon T-H, et al. A bipolar host containing 1,2,3-triazole for realizing highly efficient phosphorescent organic light-emitting diodes. New J Chem. 2010;34:1317–1322. DOI:10.1039/c0nj00091d.
   Web of Science ®Google Scholar
• Tome AC. Product class 13: 1,2,3-triazole. In: Storr RC, Gilchrist TL, editors. Science of synthesis. New York: Thieme; 2004. p. 415–601.
   Google Scholar
• Juríček M, Kouwer PHJ, Rowan AE. Triazole: a unique building block for the construction of functional materials. Chem Commun. 2011;47:8740–8749. DOI:10.1039/c1cc10685f.
   PubMed Web of Science ®Google Scholar
• Cristiano R, De Oliveira Santos DMP, Conte G, et al. 1,4-Diaryl and Schiff’s base [1,2,3]-triazole derivative liquid crystalline compounds. Liq Cryst. 2006;33:997–1003. DOI:10.1080/02678290600916138.
   Web of Science ®Google Scholar
• Srividhya D, Manjunathan S, Thirumaran S, et al. Synthesis and characterization of [1,2,3]-triazole containing liquid crystals through click reaction. J Mol Struct (Theochem). 2009;927:7–13. DOI:10.1016/j.molstruc.2009.01.035.
   Web of Science ®Google Scholar
• Park S, Ryu M-H, Shin TJ, et al. Smectic assemblies in C3-symmetric hexa-alkylated liquid crystals: transformation from smectogen to discogen via hydrogen bonding. Soft Matter. 2014;10:5804–5809. DOI:10.1039/C4SM00919C.
   PubMed Web of Science ®Google Scholar
• Gimeno N, Martín-Rapún R, Rodríguez-Conde S, et al. ‘‘Click chemistry’’ as a versatile route to synthesize and modulate bent-core liquid crystalline materials. J Mater Chem. 2012;22:16791–16800. DOI:10.1039/c2jm33612j.
   Web of Science ®Google Scholar
• Benbayer C, Kheddam N, Saïdi-Besbes S, et al. Synthesis and mesomorphic properties of novel [1,2,3] triazole mesogenic based compounds. J Mol Struct (Theochem). 2013;1034:22–28. DOI:10.1016/j.molstruc.2012.09.020.
   Web of Science ®Google Scholar
• Benbayer C, Saïdi-Besbes S, Grelet E, et al. Structure–property study of new [1,2,3]-triazole liquid crystalline derivatives. Liq Cryst. 2013;40:1520–1528. DOI:10.1080/02678292.2013.822111.
   Web of Science ®Google Scholar
• Han K, Cho B-K. Monoclinic to two-dimensional hexagonal transformation in hexacatenar molecules with a 1,2,3-triazole-based conjugated rod: morphology-dependent thermochromic behavior. Soft Matter. 2014;10:7588–7594. DOI:10.1039/C4SM01051E.
   PubMed Web of Science ®Google Scholar
• Choi J-W, Han J-H, Ryu M-H, et al. Oblique columnar assemblies of polycatenar molecules via click chemistry. Bull Korean Chem Soc. 2011;32:781–782. DOI:10.5012/bkcs.2011.32.3.781.
   Web of Science ®Google Scholar
• Lehmann M, Jahr M. New ABC core for the synthesis of nonsymmetric star molecules. Org Lett. 2006;8:721–723. DOI:10.1021/ol0528585.
   PubMed Web of Science ®Google Scholar
• Haynes WN. CRC handbook of chemistry and physics. 93rd ed. Boca Raton: CRC Press; 2012.
   Google Scholar
• Noelting E, Michel O. Direkte Ueberführung von Aminen in Diazoimide mittels Stickstoffwasserstoffsäure. Ber Dtsch Chem Ges. 1893;26:86–87. DOI:10.1002/(ISSN)1099-0682.
   Google Scholar
• Choi E-J, Xu F, Son J-H, et al. Synthesis and luminescence properties of a Lollipop-shaped molecule combined with rod and disc-like mesogens. Mol Cryst Liq Cryst. 2011;551:60–68. DOI:10.1080/15421406.2011.600141.
   Web of Science ®Google Scholar