How to cite this paper
Meena, L., Sharma, V., Mali, H & Soni, J. (2024). Synthesis and characterization of acrylamide substituted sulfanilamide based calamitic LCs: effect of terminal group on phase behavior.Current Chemistry Letters, 13(2), 391-402.
Refrences
1. Bisoyi, H. K., and Li, Q. (2021) Liquid crystals: versatile self-organized smart soft materials. Chem. Rev., 122 (5) 4887-4926.
2. Ghosh, T., and Lehmann, M. (2017) Recent advances in heterocycle-based metal-free calamitics. J. Mater. Chem. C., 5 (47) 12308-12337.
3. Koh, T. M., Ha, S. T., Lee, T. L., Lee, S. L., Yeap, G. Y., Lin, H. C., and Subramaniam, R. T. (2011) Synthesis and mesomorphic evaluation of new calamitic liquid crystals containing benzothiazole core. Chin. Chem. Lett., 22 (5) 619-622.
4. Madsen, L. A., Dingemans, T. J., Nakata, M., and Samulski, E. T. (2004) Thermotropic biaxial nematic liquid crystals. Phys. Rev. Lett., 92 (14), 145505.
5. Patel, R. B., Patel, V. R., and Doshi, A. V. (2012) Synthesis and mesomorphism of novel liquid-crystalline isobutyl-p-(p′-n-alkoxy cinnamoyloxy) cinnamates. Mol. Cryst. Liq. Cryst., 552 (1) 3-9.
6. Woltman, S. J., Jay, G. D. and Crawford, G. P. (2007) Liquid-crystal materials find a new order in biomedical applications. Nat. Mater., 6 (12) 929-938.
7. Sharma, V. S. and Patel, R. B. (2017) Synthesis and study of mesomorphic properties in rod-like chalconyl compounds. Mol. Cryst. Liq. Cryst., 643 (1) 52-61.
8. Sharma, V. S., Vekariya, R. H., Sharma, A. S. and Patel, R. B. (2017) Mesomorphic properties of liquid crystalline compounds with chalconyl central linkage in two phenyl rings. Liq. Cryst. Today, 26 (3) 46-54.
9. Matsukizono, H., Iwamatsu, K., Endo, S., Okumura, Y., Anan, S. and Kikuchi, H. (2023) Synthesis of liquid crystals bearing 1, 3-dioxane structures and characterization of their ferroelectricity in the nematic phase. J. Mater. Chem. C, 11 (18) 6183-6190.
10. Sato, M., Nagano, S. and Seki, T. (2009) A photoresponsive liquid crystal based on (1-cyclohexenyl) phenyldiazene as a close analogue of azobenzene. Chem. Comm., (25) 3792-3794.
11. Gan, S. M., Yuvaraj, A. R., Lutfor, M. R., Mashitah, M. Y. and Gurumurthy, H. (2015) Synthesis, liquid crystal characterization and photo-switching studies on fluorine substituted azobenzene based esters. RSC adv., 5 (9) 6279-6285.
12. Rahman, M.S., Wolter, T., Tripathi, A., Abbott, N.L., Mavrikakis, M. and Twieg, R.J. (2022) Investigation of the mesogenic behavior of alkoxy and fluorine tail terminated alkoxy nitrobiphenyls for chemoresponsive liquid crystals. Liq. Cryst., 49 (15) 2082-2094.
13. Bisoyi, H.K. and Kumar, S. (2010) Discotic nematic liquid crystals: science and technology. Chem. Soc. Rev., 39 (1) 264-285.
14. Viney, C., Twieg, R. J., Russell, T. P. and Depero, L. E. (1989) The structural basis of transitions between highly ordered smectic phases in semifluorinated alkanes. Liq. Cryst., 5 (6) 1783-1788.
15. Foo, K. L., Ha, S. T. and Yeap, G. Y. (2022) Synthesis and phase transition behavior of calamitic liquid crystals containing heterocyclic core and lateral ethoxy substituent. Ph. Transit., 95 (2) 178-192.
16. Desai, V., Sharma, V. S., Shah, R. R., Meena, L., Mali, H. and Patel, R. B. (2022) Synthesis and characterization of newly syringaldehyde based chalcone liquid crystals. Mol. Cryst. Liq. Cryst., 745 (1) 1-15.
17. Desai, V., Sharma, V. S. and Patel, R. B. (2018) Synthesis and study of novel biological active chalconyl-ester based bent-core LCs: Effect of tail/lateral group. Mol. Cryst. Liq. Cryst., 668 (1) 29-47.
18. Srinivasa, H.T. and Kumar, S. (2017) Synthesis and characterization of some new chalcone liquid crystals. Liq. Cryst., 44 (10) 1506-1514.
19. Sasidharan, A.K., Mathew, J., Achalkumar, A.S. and Mathews, M. (2022) Synthesis and Liquid Crystalline Properties of Low Molecular Weight Bis-Chalcone Compounds. Curr. Org. Synth., 19 (3) 463-475.
20. Nakum, K.J., Katariya, K.D., Hagar, M. and Jadeja, R.N. (2022) The influence of lateral hydroxyl group and molecular flexibility on the mesogenic behaviour of a new homologous series based on thiophene-chalcone: Synthesis, characterization, crystal structure and DFT study. J. Mol. Str., (1261) 132891.
21. Thaker, B. T., Patel, P. H., Vansadiya, A. D. and Kanojiya, J. B. (2009) Substitution effects on the liquid crystalline properties of thermotropic liquid crystals containing Schiff base chalcone linkages. Mol. Cryst. liq. Cryst., 515 (1) 135-147.
22. Chaudhari, M., Sharma, V.S., Ganga, V.S.R., Sharma, A.S., Mali, H. and Shrivastav, P.S., (2022) Room temperature imidazolium linked chalcone based ionic LCs: Role of terminal position on mesomorphism. J. Mol. Str., (1270) 133834.
23. Yang, X., Jin, X., Zhao, T. and Duan, P. (2021) Circularly polarized luminescence in chiral nematic liquid crystals: generation and amplification. Mater. Chem. Front., 5 (13) 4821-4832.
24. d’Alessandro, A. and Asquini, R. (2021) Light propagation in confined nematic liquid crystals and device applications. Appl. Sci., 11 (18) 8713.
25. Tripathi, P. K., Singh, D. P., Yadav, T., Singh, V., Srivastava, A. K., and Negi, Y. S. (2023) Enhancement of birefringence for liquid crystal with the doping of ferric oxide nanoparticles. Opt. Mater., (135) 113298.
26. Apaydın, S., and Török, M. (2019) Sulfonamide derivatives as multi-target agents for complex diseases. Bioorganic Med. Chem. Lett., 29 (16) 2042-2050.
27. Shim, W. S., Kim, S. W., and Lee, D. S. (2006) Sulfonamide-based pH-and temperature-sensitive biodegradable block copolymer hydrogels. Biomacromolecules, 7 (6) 1935-1941.
28. Supuran, C. T. (2003) Indisulam: an anticancer sulfonamide in clinical development. Expert Opin. Investig. Drugs., 12 (2) 283-287.
29. Kashyap, D., Patel, S., Prajapat, V., Sharma, V., and Vasava, D. (2019) Effect of the linking unit on the calamitic-shaped liquid crystal: a comparative study of two homologous series of benzoate and cinnamate linked compounds. Mol. Cryst. Liq. Cryst., 681 (1) 58-70.
30. Desai, V., Sharma, V. S., and Patel, R. B. (2018) Synthesis and study of novel biological active chalconyl-ester based bent-core LCs: Effect of tail/lateral group. Mol. Cryst. Liq. Cryst., 668 (1) 29-47.
31. Thakor, A., Dwivedi, D. J., Desai, V., Jadeja, U. H., Sharma, V. S., and Patel, R. B. (2022) Synthesis and characterization of biphenyl-based azo liquid crystals and its optical properties: effect of lateral and tail group. Mol. Cryst. Liq. Cryst., 726 (1) 8-26.
32. Gao, M., Ma, L., and Luo, J. (2016) Effect of alkyl chain length on the orientational behavior of liquid crystals nano-film. Tribol. Lett., (62) 1-7.
33. Sharma, V. S., and Patel, R. B. (2017) Effect of alkyl chain in the terminal ester group on mesomorphic properties of new rod like homologous series: Synthesis and characterization. Mol. Cryst. Liq. Cryst., 643 (1) 62-75.
34. Wang, S., Zhang, C., & Chang, Q. (2017). Synthesis of magnetic crosslinked starch-graft-poly (acrylamide)-co-sodium xanthate and its application in removing heavy metal ions. J. Exp. Nano sci., 12 (1) 270-284.
35. Mani, B., and Kathavarayan, S. (2016) Studies on photocrosslinking and flame‐retardant properties of chalcone‐based polyacrylamides. Polym. Adv. Technol., 27 (4) 466-476.
36. Imrie, C. T., and Taylor, L. (1989) The preparation and properties of low molar mass liquid crystals possessing lateral alkyl chains. Liq. Cryst., 6(1), 1-10.
37. Bisoyi, H. K., and Li, Q. (2021) Liquid crystals: versatile self-organized smart soft materials. Chem. Rev., 122 (5) 4887-4926.
38. Jafari Ozumchelouei, E., Hamidian, A. H., Zhang, Y., and Yang, M. (2020) Physicochemical properties of antibiotics: A review with an emphasis on detection in the aquatic environment. Water Environ. Res., 92 (2) 177-188.
39. Arshad, M. N., Faidallah, H. M., Asiri, A. M., Kosar, N., & Mahmood, T. (2020). Structural, spectroscopic and nonlinear optical properties of sulfonamide derivatives; experimental and theoretical study. J. Mol. Str., (1202) 127393.
40. Suthar, D. M., Doshi, A. A., and Doshi, A. V. (2013) Study of liquid crystalline state and evaluation of its properties through a novel Homologous series. Mol. Cryst. Liq. Cryst., 582 (1) 79-87.
41. Patari, S., Chakraborty, S., and Nath, A. (2016) The optical anisotropy and orientational order parameter of two mesogens having slightly different flexible side chain–a comparative study. Liq. Cryst., 43 (8) 1017-1027.
42. Niemczak, M., Rzemieniecki, T., Sobiech, Ł., Skrzypczak, G., Praczyk, T., and Pernak, J. (2019) Influence of the alkyl chain length on the physicochemical properties and biological activity in a homologous series of dichlorprop-based herbicidal ionic liquids. J. Mol. Liq., 276, 431-440.