Synthesis, Characterization, and Antioxidant Activity of a New Copper(II)-imidazole Derivative Complex

Degenerative diseases such as cancer, cataract, and cerebral dysfunction are increasingly associated with free radicals. Copper(II) complexes exhibit antioxidant activity and can act in the treatment of these diseases altering or inhibiting cellular functions by intercalations with nitrogenous bases of DNA. Those complexes can be employed in the development of new drugs and materials for the treatment of these diseases or as preventive agents. In this work, we present the synthesis and characterization of a complex formed by an imidazole-type ligand and copper(II). NMR data confirm the structure of ligand and that its interaction with copper(II) ions produces the complex [Cu(3NIMDZ-H)(OH2)5](ClO4)2 with a coordinated binding between copper(II) ion and nitrogen of the imidazole ring. Density functional theory (DFT) calculations performed at the B3LYP-D3(BJ)/def2-SVP level of theory for both the complex and ligand reveal that the formation of the complex is spontaneous, exhibiting a copper-nitrogen bond length of 1.988 Å. The antioxidant assays showed a high-speed inhibition of complex radicals regarding free ligand. IC50 value is 1.5 times higher than the BHT standard, demonstrating the high antioxidant power of this compound. [Cu(3NIMDZ-H)(OH2)5]2+ shows a fast kinetics behavior for DPPH inhibition, which shows the possibility of new material application in antitumoral drug development.

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Journal
Orbital - The Electronic Journal of Chemistry
Published
2025-05-17
DOI
https://doi.org/10.17807/orbital.v17i2.19507
Primary Topic
Synthesis and biological activity
Type
article
Field-Weighted Citation Impact
0.00

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article

Synthesis, Characterization, and Antioxidant Activity of a New Copper(II)-imidazole Derivative Complex

Francisco B. Pereira, Ariel C. de Oliveira, José Roberto Miranda Júnior, André Luiz Tessaro et al.
Orbital - The Electronic Journal of Chemistry
Synthesis and biological activity
article

Synthesis, Characterization, and Antioxidant Activity of a New Copper(II)-imidazole Derivative Complex

Francisco B. Pereira, Ariel C. de Oliveira, José Roberto Miranda Júnior, André Luiz Tessaro, Lilian Tatiani Düsman Tonin, Rafael Block Samulewski, Ana Claudia Pedrozo da Silva, Antonio G. S. de Oliveira‐Filho
article en

Abstract

Degenerative diseases such as cancer, cataract, and cerebral dysfunction are increasingly associated with free radicals. Copper(II) complexes exhibit antioxidant activity and can act in the treatment of these diseases altering or inhibiting cellular functions by intercalations with nitrogenous bases of DNA. Those complexes can be employed in the development of new drugs and materials for the treatment of these diseases or as preventive agents. In this work, we present the synthesis and characterization of a complex formed by an imidazole-type ligand and copper(II). NMR data confirm the structure of ligand and that its interaction with copper(II) ions produces the complex [Cu(3NIMDZ-H)(OH2)5](ClO4)2 with a coordinated binding between copper(II) ion and nitrogen of the imidazole ring. Density functional theory (DFT) calculations performed at the B3LYP-D3(BJ)/def2-SVP level of theory for both the complex and ligand reveal that the formation of the complex is spontaneous, exhibiting a copper-nitrogen bond length of 1.988 Å. The antioxidant assays showed a high-speed inhibition of complex radicals regarding free ligand. IC50 value is 1.5 times higher than the BHT standard, demonstrating the high antioxidant power of this compound. [Cu(3NIMDZ-H)(OH2)5]2+ shows a fast kinetics behavior for DPPH inhibition, which shows the possibility of new material application in antitumoral drug development.

Orbital - The Electronic Journal of Chemistry
Universidade Tecnológica Federal do Paraná (BR)
Fundação de Amparo à Pesquisa do Estado de São Paulo, Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Conselho Nacional de Desenvolvimento Científico e Tecnológico
Openalex Percentile: Top 91%
Synthesis and biological activity
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