Electrochemical Behavior and Complexation of Hexamethanol-Linked Triazine Ligand with Mn(II) Ions: Insights from Cyclic Voltammetry and Thermodynamic Studies

Document Type : Original Article

Authors

1 Chemistry Department, Faculty of Science, Mansoura University, Mansoura, Egypt, 35516

2 Chemistry Department, Faculty of Science, Mansoura University, Egypt

3 chemistry department, faculty of science, Mansoura University, Egypt

Abstract

In this study, the electrochemical behaviour of the ligand ((1,3,5-triazine-2,4,6-triyl)tris(azanetriyl))hexamethanol (H6L) and its complexation with Mn(II) ions was reviewed using cyclic voltammetry and thermodynamic studies. The ligand showed one oxidation peak in a KCl solution with an irreversible system. The binding interactions between ligand and manganese chloride were examined by monitoring the shifts in redox potential and peak current, providing the complex formation. The introduction of catechol is a significant to the electrochemical response of Mn (L) complex. The most stable ratio in solution was 3:1 metal : ligand. Thermodynamic analyses showed that the formation of the complex in solution was further investigated using parameters such as the stability constant (βj) and Gibbs free energy (ΔG), revealing a stable 3:1 metal-to-ligand molar ratio for the Mn (L) complex.

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Articles in Press, Accepted Manuscript
Available Online from 01 February 2026
  • Receive Date: 19 June 2025
  • Revise Date: 07 September 2025
  • Accept Date: 14 September 2025