Novel Cr(III), Ni(II), and Zn(II) complexes of thiocarbamide derivative: Synthesis, investigation, theoretical, catalytic, potentiometric, molecular docking and biological studies

Throughout this research, the thiocarbamide derivative (H2L), and its Cr(III), Ni(II) and Zn(II) complexes have been reported. The thiocarbamide moiety was established with a reaction of benzoyl isothiocyanate and 1H-1,2,4-triazol-3-amine. Structural elucidation of such compounds was achieved using...

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Main Author: Zehbah Ali Mohammed Al-Ahmed
Format: Article
Language:English
Published: Elsevier 2022-09-01
Series:Arabian Journal of Chemistry
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S1878535222004208
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author Zehbah Ali Mohammed Al-Ahmed
author_facet Zehbah Ali Mohammed Al-Ahmed
author_sort Zehbah Ali Mohammed Al-Ahmed
collection DOAJ
description Throughout this research, the thiocarbamide derivative (H2L), and its Cr(III), Ni(II) and Zn(II) complexes have been reported. The thiocarbamide moiety was established with a reaction of benzoyl isothiocyanate and 1H-1,2,4-triazol-3-amine. Structural elucidation of such compounds was achieved using elementary examination, spectral and magnetic experiments. The octahedral construction of the Cr(III) complex, the tetrahedral geometry of the Zn(III) complex and the mixed geometry (tetrahedral and square planar) of the Ni(II) complex have been verified by the optimization of structure using DFT. The action of Zn2+ complex in the oxidative degradation of an organic azo-dye was investigated, and it showed promising results. The thermal degradation behavior of thiocarbamide metal complexes were studied as well as the calculation of the kinetic data for title compounds (Ea, A, ΔH*, ΔS* and ΔG*) of thermal degradation steps has been tested utilizing two different techniques. Liver carcinoma (HePG2) and breast carcinoma (MCF-7) cytotoxicity as well as ABTS-antioxidant activities demonstrated the effective inhibitory of the Ni(II)-complex relative to other tested compounds. The antimicrobial activity of the compounds suggests that Cr(III) has the highest activity. Furthermore, the Molecular Operating Environment (MOE) program was used to calculate the binding affinity between the EGFR protein and the compounds under investigation.
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spelling doaj.art-f23620ebfafe4e7e8dd4d45b8966a9ff2022-12-22T02:11:42ZengElsevierArabian Journal of Chemistry1878-53522022-09-01159104104Novel Cr(III), Ni(II), and Zn(II) complexes of thiocarbamide derivative: Synthesis, investigation, theoretical, catalytic, potentiometric, molecular docking and biological studiesZehbah Ali Mohammed Al-Ahmed0Department of Chemistry, College of Sciences and arts, Dhahran Aljanoub, King Khalid University, Abha, Saudi ArabiaThroughout this research, the thiocarbamide derivative (H2L), and its Cr(III), Ni(II) and Zn(II) complexes have been reported. The thiocarbamide moiety was established with a reaction of benzoyl isothiocyanate and 1H-1,2,4-triazol-3-amine. Structural elucidation of such compounds was achieved using elementary examination, spectral and magnetic experiments. The octahedral construction of the Cr(III) complex, the tetrahedral geometry of the Zn(III) complex and the mixed geometry (tetrahedral and square planar) of the Ni(II) complex have been verified by the optimization of structure using DFT. The action of Zn2+ complex in the oxidative degradation of an organic azo-dye was investigated, and it showed promising results. The thermal degradation behavior of thiocarbamide metal complexes were studied as well as the calculation of the kinetic data for title compounds (Ea, A, ΔH*, ΔS* and ΔG*) of thermal degradation steps has been tested utilizing two different techniques. Liver carcinoma (HePG2) and breast carcinoma (MCF-7) cytotoxicity as well as ABTS-antioxidant activities demonstrated the effective inhibitory of the Ni(II)-complex relative to other tested compounds. The antimicrobial activity of the compounds suggests that Cr(III) has the highest activity. Furthermore, the Molecular Operating Environment (MOE) program was used to calculate the binding affinity between the EGFR protein and the compounds under investigation.http://www.sciencedirect.com/science/article/pii/S1878535222004208ThiocarbamideTriazoleComplexesStructural optimizationBiological assay
spellingShingle Zehbah Ali Mohammed Al-Ahmed
Novel Cr(III), Ni(II), and Zn(II) complexes of thiocarbamide derivative: Synthesis, investigation, theoretical, catalytic, potentiometric, molecular docking and biological studies
Arabian Journal of Chemistry
Thiocarbamide
Triazole
Complexes
Structural optimization
Biological assay
title Novel Cr(III), Ni(II), and Zn(II) complexes of thiocarbamide derivative: Synthesis, investigation, theoretical, catalytic, potentiometric, molecular docking and biological studies
title_full Novel Cr(III), Ni(II), and Zn(II) complexes of thiocarbamide derivative: Synthesis, investigation, theoretical, catalytic, potentiometric, molecular docking and biological studies
title_fullStr Novel Cr(III), Ni(II), and Zn(II) complexes of thiocarbamide derivative: Synthesis, investigation, theoretical, catalytic, potentiometric, molecular docking and biological studies
title_full_unstemmed Novel Cr(III), Ni(II), and Zn(II) complexes of thiocarbamide derivative: Synthesis, investigation, theoretical, catalytic, potentiometric, molecular docking and biological studies
title_short Novel Cr(III), Ni(II), and Zn(II) complexes of thiocarbamide derivative: Synthesis, investigation, theoretical, catalytic, potentiometric, molecular docking and biological studies
title_sort novel cr iii ni ii and zn ii complexes of thiocarbamide derivative synthesis investigation theoretical catalytic potentiometric molecular docking and biological studies
topic Thiocarbamide
Triazole
Complexes
Structural optimization
Biological assay
url http://www.sciencedirect.com/science/article/pii/S1878535222004208
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