Synthesis, Spectroscopic, Biological and DFT Studies of 2,4,6-Tris(4-Carboxyphenylimino-41-Formylphenoxy)-1,3,5-Triazine and its Trinuclear Dy(III) and Er(III) Salen Capped Complexes

Authors

  • Uchechukwu Susan Oruma

    University of Nigeria, Nsukka, 410001, Nigeria
    Author
  • Pius Oziri Ukoha

    University of Nigeria, Nsukka, 410001, Nigeria
    Author
  • Collins U. Ibeji

    University of Nigeria, Nsukka, 410001, Nigeria
    Author
  • Lawrence Nnamdi Obasi

    University of Nigeria, Nsukka, 410001, Nigeria
    Author
  • Obinna C. Okpareke

    University of Nigeria, Nsukka, 410001, Nigeria
    Author
  • Ebubechukwu N. Dim

    University of Nigeria, Nsukka, 410001, Nigeria
    Author
  • Klaus Jurkschat

    Technische Universität, Fakultät für Chemie und Chemische Biologie, -44221 Dortmund, Germany.
    Author
  • Ponnadurai Ramasami

    University of Johannesburg, Doornfontein, Johannesburg 2028, South Africa
    Author

Keywords:

Tripodal Schiff base, 1,3,5-triazine, trinuclearDy/Er(III) complexes, antimicrobial activity, antimalarial activity, DFT, docking

Abstract

Uchechukwu S. Oruma, Pius O. Ukoha, Collins U. Ibeji, Lawrence N. Obasi, Obinna C. Okpareke, Ebubechukwu N. Dim, Klaus Jurkschat and Ponnadurai Ramasami

A tripodal Schiff base ligand, 2,4,6-tris(4-carboxyphenylimino-41-formylphenoxy)-1,3,5-triazine (H3CT) and its trinuclear Dy(III) and Er(III) complexes were synthesized. Characterization of these compounds was done via UV-Visible, IR, 1H, and 13C NMR spectroscopies, elemental analysis, and molar conductivity measurements. The spectral studies indicate that the ligand is hexadentate and coordinates to Dy/Er(III) ions through the oxygen atoms of the carboxylic group. The trinuclear complexes were characterized as being bridged by a carboxylic group to the Dy(III) and Er(III) salen centers and display a coordination number of six. Biological studies revealed that the Dy(III) complex showed the highest activity against tested microorganisms and also gave the highest percentage parasitemia inhibition (84.0 %) relative to Artesunate (87.2 %). DFT calculations were carried out to enhance understanding of H3CT at the molecular level based on  (B3LYP)/6-31+G(d,p). The molecular docking results revealed the binding mode of H3CT complexed with Staphylococcus aureus.

Author Biographies

  • Uchechukwu Susan Oruma, University of Nigeria, Nsukka, 410001, Nigeria

    Coordination Chemistry and Inorganic Pharmaceuticals Unit,

    Department of Pure and Industrial Chemistry

  • Pius Oziri Ukoha, University of Nigeria, Nsukka, 410001, Nigeria

    Coordination Chemistry and Inorganic Pharmaceuticals Unit,

    Department of Pure and Industrial Chemistry

  • Collins U. Ibeji, University of Nigeria, Nsukka, 410001, Nigeria

    Department of Pure and Industrial Chemistry

  • Lawrence Nnamdi Obasi, University of Nigeria, Nsukka, 410001, Nigeria

    Department of Pure and Industrial Chemistry

  • Obinna C. Okpareke, University of Nigeria, Nsukka, 410001, Nigeria

    Department of Pure and Industrial Chemistry

  • Ebubechukwu N. Dim, University of Nigeria, Nsukka, 410001, Nigeria

    Department of Pure and Industrial Chemistry,

     

  • Ponnadurai Ramasami, University of Johannesburg, Doornfontein, Johannesburg 2028, South Africa

    Department of Applied Chemistry

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Published

2021-09-21

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