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Synthesis, Crystal Structure and Comparative Study on the Removal of Cationic Dyes Using Different Amide and Amine Groups

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Abstract

Two crystalline materials C18H16N3O3 (1) and C10H8N2⋅C8H7NO4 (2) have been synthesized under solvothermal conditions with different time and temperatures. The structure of 1 have been determined by single-crystal X-ray diffraction analysis. Both structures were also characterized by FT-IR, powder X-ray diffraction (PXRD), thermogravimetric analysis (TGA), and Field Emission Scanning Electron Microscopy (FESEM) techniques. Both crystals are constructed from the same organic ligand (2-aminoterephthalic acid and 4,4-bipyridine), however, they present varied functional groups, amide for 1 and amine for 2, indicating formylation of NH2 groups of organic linkers during the synthesis process in 1. The adsorption potential of the samples for cationic methyl violet (MV) and methylene blue (MB) dyes uptake from aqueous solution was examined by UV–Vis spectrophotometer. The result showed that the adsorption rate of these cationic dyes with 1 containing amide group is higher than 2 with amine group, due to stronger acid-base interaction between amides and cationic dyes.

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Authors and Affiliations

  1. Department of Chemistry, Science and Research Branch, Islamic Azad University, Tehran, Iran

    Saeideh Tavakoli

  2. School of Chemistry, College of Science, University of Tehran, Tehran, Iran

    Alireza Abbasi

  3. Department of Chemistry, Faculty of Pharmaceutical Chemistry, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran

    Mohammad Yousefi

  4. Department of Chemistry, Faculty of Science, Azarbaijan Shahid Madani University, Tabriz, Iran

    Moayad Hossaini Sadr

Authors
  1. Saeideh Tavakoli
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  2. Alireza Abbasi
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  3. Mohammad Yousefi
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  4. Moayad Hossaini Sadr
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Correspondence to Alireza Abbasi.

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Tavakoli, S., Abbasi, A., Yousefi, M. et al. Synthesis, Crystal Structure and Comparative Study on the Removal of Cationic Dyes Using Different Amide and Amine Groups. Crystallogr. Rep. 67, 1207–1213 (2022). https://doi.org/10.1134/S1063774522070124

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  • DOI: https://doi.org/10.1134/S1063774522070124

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