Bioactive porphyrin magnesium (II) complex. Synthesis, molecular structure and spectroscopic characterization. Biological activity and molecular docking studies

• Published in: Polyhedron 2024-03, Vol.250, p.116815, Article 116815
• Main Authors: Alanazi, Amal N., Ezzayani, Khaireddine, Ben Khelifa, Arbia, Mansour, Anissa, Alanazi, Reem, Eltoom Abdalla Hussein, Ishraga, Hajlaoui, Khaoula, Abdelbasit Nory Salih, Magdah
• Format: Article
• Language: English
• Subjects: Antibacterial activity; Magnesium porphyrins complexes; Molecular MOE docking; Porphyrin structure; X-ray molecular structure
• ISSN: 0277-5387
• DOI: 10.1016/j.poly.2023.116815

[Display omitted] We have synthesized and characterized porphyrin structures by UV–visible, IR and fluorescence spectroscopy studies and single crystal XRD analysis; H2(TPP) (I) (meso-tetraphenylporphyrin), [Mg(TPP)(DMF)] (II); (DMF: dimethylformamide) and [Mg(TPP)(H2O)]0.2(4-CNpy) (III); (4-CNpy: 4-Cyanopyridine). The crystal packing of the porphyrin structures is stabilized by intermolecular hydrogen bonds and by intermolecular CH⋯Cg π interactions where Cg is the centroid of the phenyl and pyrrole rings. UV–Vis spectroscopic data confirmed the creation of Mg-meso-porphyrin complexes by the red-shifted Soret bands for our derivatives compared to the free-base porphyrin. The optical gap energy values of (I), (II) and (III) are 1.92, 2.07 and 2.00 eV. Gram-positive and Gram-negative bacteria were tested against free porphyrin (I), metallated porphyrin (II) and complex (III). The results show that the magnesium porphyrin derivative is highly effective compared to H2TPP free-base porphyrins and metallated porphyrin [Mg(TPP)] and has higher inhibition character against the tested bacteria. The molecular docking of the complex (III), in the active sites of bacterial proteins was carried out to detect the degree of antibacterial activity of recognition.