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2022 | 169 | 43-54

Article title

Columnar liquid crystals based on the lower rim functionalization on resorcin[4]arene core

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EN

Abstracts

EN
Lower rim functionalized resorcin[4]arene derivatives were synthesized by four different n-alkyl chain spacers. All four derivatives have been characterized by using Fourier transform infrared (FT-IR) and Nuclear magnetic resonance (NMR) spectroscopic technique. The liquid crystalline properties of these synthesized compounds were studied by POM investigation. All derivatives exhibited columnar hexagonal type mesophase with broad temperature range. The mesomorphic properties were further influenced by variable side alkoxy chain (-OR). Compounds CR1 showed higher temperature range mesophase as compared to compound CR4.

Year

Volume

169

Pages

43-54

Physical description

Contributors

  • Department of Chemistry, School of Sciences, Gujarat University, Ahmedabad, Gujarat, India
  • Department of Chemistry, School of Sciences, Gujarat University, Ahmedabad, Gujarat, India
  • Department of Chemistry, School of Sciences, Gujarat University, Ahmedabad, Gujarat, India
  • Department of Chemistry, School of Sciences, Gujarat University, Ahmedabad, Gujarat, India

References

  • [1] Kumar K.A., Renuka N., Pavithra G., Kumar G.V., Comprehensive review on coumarins: Molecules of potential chemical and pharmacological interest. Journal of Chemical and Pharmaceutical Research 7(9) (2015) 67-81
  • [2] (a) Stenull O, Lubensky T,C., Director Fluctuations in Two-Dimensional Liquid Crystal Disclinations. Crystals. 12(1) (2021) 1. (b) Shen Y., Dierking I., Recent Progresses on Experimental Investigations of Topological and Dissipative Solitons in Liquid Crystals. Crystals 12(1) (2022) 94
  • [3] Stupp S.I., Palmer L.C., Supramolecular chemistry and self-assembly in organic materials design. Chemistry of Materials 26(1) (2014) 507-518
  • [4] Tu Y., Peng F., Adawy A., Men Y., Abdelmohsen L.K., Wilson D.A., Mimicking the cell: bio-inspired functions of supramolecular assemblies. Chemical Reviews 116(4) (2016) 2023-2078
  • [5] Iliopoulos K., Krupka O., Gindre D., Sallé M., Reversible two-photon optical data storage in coumarin-based copolymers. Journal of the American Chemical Society. 132(41) (2010) 14343-14345
  • [6] Chen M.X., Li T., Peng S., Tao D., Supramolecular nanocapsules from the self-assembly of amphiphilic calixarene as a carrier for paclitaxel. New Journal of Chemistry 40(12) (2016) 9923-9929
  • [7] Nimse S.B., Kim T., Biological applications of functionalized calixarenes. Chemical Society Reviews 42(1) (2013) 366-386
  • [8] Sharma V.S., Shah A.P., Sharma A.S., A new class of supramolecular liquid crystals derived from azo calix [4] arene functionalized 1,3,4-thiadiazole derivatives. New Journal of Chemistry 43(8) (2019) 3556-3564
  • [9] Delahousse G., Lavendomme R., Jabin I., Agasse V., Cardinael P., Calixarene-based stationary phases for chromatography. Current Organic Chemistry 19(23) (2015) 2237-2249
  • [10] Auzelyte V., Langner A., Solak H.H., Thermal development of a calixarene resist. Journal of Vacuum Science & Technology B: Microelectronics and Nanometer Structures Processing, Measurement, and Phenomena 27(6) (2009) 2990-2992
  • [11] Li X.Z., Zhou L.P., Yan L.L., Dong Y.M., Bai Z.L., Sun X.Q., Diwu J., Wang S., Bünzli J.C., Sun Q.F., A supramolecular lanthanide separation approach based on multivalent cooperative enhancement of metal ion selectivity. Nature Communications. 9(1) (2018) 1-10
  • [12] Sharma V.S., Sharma A.S., Agarwal N.K., Shah P.A., Shrivastav P.S., Self-assembled blue-light emitting materials for their liquid crystalline and OLED applications: from a simple molecular design to supramolecular materials. Molecular Systems Design & Engineering 5(10) (2020) 1691-1705
  • [13] Gole B., Shanmugaraju S., Bar A.K., Mukherjee P.S., Supramolecular polymer for explosives sensing: role of H-bonding in enhancement of sensitivity in the solid state. Chemical Communications 47(36) (2011) 10046-10048
  • [14] Matsuo Y., Sato Y., Niinomi T., Soga I., Tanaka H., Nakamura E., Columnar structure in bulk heterojunction in solution-processable three-layered pin organic photovoltaic devices using tetrabenzoporphyrin precursor and silylmethyl [60] fullerene. Journal of the American Chemical Society 131(44) (2009) 16048-16050
  • [15] Li X.L., Yu S., Chen M.N., Jiang M., Wang R.Z., Xing L.B., Artificial light-harvesting supramolecular assemblies with controllable fluorescence intensity formed by cyclodextrin-based host-gost complexation. Journal of Photochemistry and Photobiology A: Chemistry 410 (2021) 113182
  • [16] Sharma V.S., Sharma A.S., Vekariya R.H., Columnar self-assembly of bowl-shaped luminscent oxadiazole calix[4]arene derivatives. Journal of Molecular Liquids 271 (2018) 319-327
  • [17] (a) Duan Z., Xu F., Huang X., Qian Y., Li H., Tian W., Crown Ether‐Based Supramolecular Polymers: From Synthesis to Self‐Assembly. Macromolecular Rapid Communications. (2021) 2100775. (b) Zhang J, Ma PX. Cyclodextrin-based supramolecular systems for drug delivery: recent progress and future perspective. Advanced Drug Delivery Reviews 65(9) (2013) 1215-1233
  • [18] Gajjar J.A., Vekariya R.H., Parekh H.M., Recent advances in upper rim functionalization of resorcin[4]arene derivatives: Synthesis and applications. Synthetic Communications 50(17) (2020) 2545-2571
  • [19] Sharma V.S., Singh H.K., Vekariya R.H., Sharma A.S., Patel R.B., Mesomorphic properties of novel supramolecular calix [4] arene Schiff base ester derivatives: design and biological investigation. Chemistry Select 2(27) (2017) 8596-8606
  • [20] Sharma V.S., Shah A.P., Sharma A.S., Athar M., Columnar self-assembly, gelation and electrochemical behavior of cone-shaped luminescent supramolecular calix[4]arene LCs based on oxadiazole and thiadiazole derivatives. New Journal of Chemistry 43(4) (2019) 1910-1925
  • [21] Gajjar J.A., Vekariya R.H., Sharma V.S., Kher S.N., Rajani D.P., Parekh H.M., Mesomorphic properties, microwave-assisted synthesis, and antimicrobial evaluation of novel Schiff base functionalized resorcin[4]arene derivatives. Molecular Crystals and Liquid Crystals 715(1) (2021) 37-55
  • [22] Sun X., James T.D., Glucose sensing in supramolecular chemistry. Chemical Reviews 115(15) (2015) 8001-8037
  • [23] Liu K., Chen S.L., Xiao S.W., Zhang X.L., Ba D.C., Wang D.Y., Du G.Y., Ba Y.S., Molecular simulation of protein transport controlled by pressure-driven flow in silica nanofluidic channels. Bulgarian Chemical Communications 47 (2015) 1221-1228
  • [24] Karami B., Khodabakhshi S., Safikhani N., Arami A., A green and highly efficient solvent-free synthesis of novel calicx [4] resorcinarene derivatives using tungstate sulfuric acid. Bulletin of the Korean Chemical Society 33(1) (2012) 123-127
  • [25] Mobinikhaledi A., Kalhor M., Ghorbani A.R., Fathinejad H., Synthesis of Resorcin [4] arenes Using Microwave Irradiation and Conventional Heating. Asian Journal of Chemistry 22(2) (2010) 1103
  • [26] Burilov A.R., Volodina Y.M., Popova E.V., Gazizov A.S., Knyazeva I.R., Pudovik M.A., Habicher V.D., Konovalov A.I., Condensation of resorcinol with phosphorylated acetals, synthesis of calix[4]resorcinolarenes with phosphorus-containing alkyl fragments in the lower rim. Russian Journal of General Chemistry 76(3) (2006) 412-416
  • [27] Pfeiffer C.R., Feaster K.A., Dalgarno S.J., Atwood J.L., Syntheses and characterization of aryl-substituted pyrogallol[4]arenes and resorcin[4]arenes. Cryst Eng Comm. 18(2) (2016) 222-229
  • [28] Payne D.T., Labuta J., Futera Z., Březina V., Hanyková L., Chahal M.K., Hill J.P., Molecular rotor based on an oxidized resorcinarene. Organic Chemistry Frontiers 9(1) (2022) 39-50
  • [29] Wang F., Qiu W., Zeng J., Yuan P., Zong W., Wu W., Liu Y., Xu S., Su S.J., Cao S., Calix [4] resorcinarene-based hyper-structured molecular thermally activated delayed fluorescence yellow-green emitters for non-doped OLEDs. Journal of Materials Chemistry C. 8(13) (2020) 4469-4476
  • [30] Eddaif L., Shaban A., Telegdi J., Szendro I., A piezogravimetric sensor platform for sensitive detection of lead (ii) ions in water based on calix [4] resorcinarene macrocycles: synthesis, characterization and detection. Arabian Journal of Chemistry. 13(2) (2020) 4448-4461
  • [31] Kashapov R.R., Razuvayeva Y.S., Ziganshina A.Y., Mukhitova R.K., Sapunova A.S., Voloshina A.D., Syakaev V.V., Latypov S.K., Nizameev I.R., Kadirov M.K., Zakharova L.Y., N-methyl-d-glucamine–calix [4] resorcinarene conjugates: Self-assembly and biological properties. Molecules 24(10) (2019) 1939
  • [32] Tang H., Guo H., Yang F., Zhu S., Synthesis and mesomorphic properties of calix [4] resorcinarene–triphenylene oligomers. Liquid Crystals 44(10) (2017) 1566-1574
  • [33] Gajjar J., Vekariya R.H., Sharma V.S., Parekh H., Synthesis, design and characterization of supramolecular self-assembly of calix [4] resorcinare substituted LCs. Molecular Crystals and Liquid Crystals 668(1) (2018) 48-58
  • [34] Han C., Guo H., Lai J., Yang F., Calix [4] resorcinarene-cholesterol columnar liquid crystals: Synthesis, mesomorphism and the influence of spacers on liquid crystalline behaviors. Journal of Molecular Liquids 231 (2017) 220-224
  • [35] M .F. J. Mabesoone, S. Kardas, H. S. Carrera, J. Barbera et al., Competitive hydrogen bonding in supramolecular polymerizations of tribenzylbenzene-1,3,5-tricarboxamides. Molecular Systems Design & Engineering 5 (4) (2020) 820-828
  • [36] Irla S., Raghunathan V. A., Kumar S., Columnar mesomorphism in heptazine discotics. Journal of Molecular Liquids 314 (2020) 113631
  • [37] Nath S., Pathak S. K., De J., Pal S. K., and Achalkumar A. S., Correction: Star-shaped π-gelators based on oxadiazole and thiadiazoles: a structure–property correlation. Molecular Systems Design & Engineering 4 (4) (2019) 984-985

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article

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bwmeta1.element.psjd-33eb7c28-26a0-425a-91f6-cc4fa9d901e2
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