SYNTHESIS, SPECTROSCOPIC CHARACTERIZATION AND PROPERTIES OF IMIDAZOLE-COPPER (II) COMPLEX

Student: Chioma Glory Chidebe
Supervisor: Prof F A Fabiyi
HOD: Dr G O Oladipo
Department of Industrial Chemistry
Natural and Applied Sciences
Achievers University, Owo, Ondo State

Abstract

This study focuses on the synthesis, characterization, and analysis of the physical and spectroscopic properties of copper(II) complexes with imidazole ligands at varying ligand-to-metal ratios (1:1, 1:2, 1:3, and 1:4). The copper-imidazole complexes were synthesized using a solution-based reaction of copper(II) sulfate with imidazole, followed by purification and drying. Characterization techniques including UV-Visible spectroscopy, Fourier Transform Infrared (FTIR) spectroscopy, and X-ray diffraction (XRD) were employed to confirm complex formation and determine structural features. The percentage yield of the complexes increased from a 1:1 to 1:2 ratio but decreased at higher ligand ratios due to coordination saturation. UV-Vis spectra revealed characteristic d-d transitions and ligand-to-metal charge transfer (LMCT) bands, with peak shifts influenced by ligand concentration and coordination geometry. FTIR spectra displayed changes in N–H and C–N vibrations, confirming metal-ligand bonding through nitrogen atoms of imidazole. Notably, Cu–N stretching bands around 598 cm⁻¹ confirmed coordination. Melting point analysis indicated high thermal stability, with values ranging from 235°C to 243°C. Solubility tests showed the complexes were insoluble in common organic solvents but soluble in water under acidic conditions (pH 3.5), indicating pH-dependent behavior. The findings suggest that increasing copper concentration improves complex stability and coordination up to an optimal ratio (1:2), beyond which aggregation and decreased yield occur. These results confirm the successful synthesis of stable, thermally robust copper(II)-imidazole complexes and highlight their potential applications in coordination chemistry, materials science, and biologically active compound development.

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