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Synthesis, Characterization, and Biological Activity of N(1)-Methyl-2-(1H-1,2,3-Benzotriazol-1-y1)-3-Oxobutan- ethioamide Complexes with Some Divalent Metal (II) Ions
A new series of Zn(2+), Cu(2+), Ni(2+), and Co(2+) complexes of N(1)-methyl-2-(1H-1,2,3-benzotriazol-1-yl)-3-oxobutanethioamide (MBOBT), HL, has been synthesized and characterized by different spectral and magnetic measurements and elemental analysis. IR spectral data indicates that (MBOBT) exists o...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2268950/ https://www.ncbi.nlm.nih.gov/pubmed/18364993 http://dx.doi.org/10.1155/2008/479897 |
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author | Al-Awadi, Nouria A. Shuaib, Nadia M. Abbas, Alaa El-Sherif, Ahmed A. El-Dissouky, Ali Al-Saleh, Esmaeil |
author_facet | Al-Awadi, Nouria A. Shuaib, Nadia M. Abbas, Alaa El-Sherif, Ahmed A. El-Dissouky, Ali Al-Saleh, Esmaeil |
author_sort | Al-Awadi, Nouria A. |
collection | PubMed |
description | A new series of Zn(2+), Cu(2+), Ni(2+), and Co(2+) complexes of N(1)-methyl-2-(1H-1,2,3-benzotriazol-1-yl)-3-oxobutanethioamide (MBOBT), HL, has been synthesized and characterized by different spectral and magnetic measurements and elemental analysis. IR spectral data indicates that (MBOBT) exists only in the thione form in the solid state while 13C NMR spectrum indicates its existence in thione and thiole tautomeric forms. The IR spectra of all complexes indicate that (MBOBT) acts as a monobasic bidentate ligand coordinating to the metal(II) ions via the keto-oxygen and thiolato-sulphur atoms. The electronic spectral studies showed that (MBOBT) bonded to all metal ions through sulphur and nitrogen atoms based on the positions and intensity of their charge transfer bands. Furthermore, the spectra reflect four coordinate tetrahedral zinc(II), tetragonally distorted copper(II), square planar nickel(II), and cobalt(II) complexes. Thermal decomposition study of the complexes was monitored by TG and DTG analyses under N(2) atmosphere. The decomposition course and steps were analyzed and the activation parameters of the nonisothermal decomposition are determined. The isolated metal chelates have been screened for their antimicrobial activities and the findings have been reported and discussed in relation to their structures. |
format | Text |
id | pubmed-2268950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-22689502008-03-24 Synthesis, Characterization, and Biological Activity of N(1)-Methyl-2-(1H-1,2,3-Benzotriazol-1-y1)-3-Oxobutan- ethioamide Complexes with Some Divalent Metal (II) Ions Al-Awadi, Nouria A. Shuaib, Nadia M. Abbas, Alaa El-Sherif, Ahmed A. El-Dissouky, Ali Al-Saleh, Esmaeil Bioinorg Chem Appl Research Article A new series of Zn(2+), Cu(2+), Ni(2+), and Co(2+) complexes of N(1)-methyl-2-(1H-1,2,3-benzotriazol-1-yl)-3-oxobutanethioamide (MBOBT), HL, has been synthesized and characterized by different spectral and magnetic measurements and elemental analysis. IR spectral data indicates that (MBOBT) exists only in the thione form in the solid state while 13C NMR spectrum indicates its existence in thione and thiole tautomeric forms. The IR spectra of all complexes indicate that (MBOBT) acts as a monobasic bidentate ligand coordinating to the metal(II) ions via the keto-oxygen and thiolato-sulphur atoms. The electronic spectral studies showed that (MBOBT) bonded to all metal ions through sulphur and nitrogen atoms based on the positions and intensity of their charge transfer bands. Furthermore, the spectra reflect four coordinate tetrahedral zinc(II), tetragonally distorted copper(II), square planar nickel(II), and cobalt(II) complexes. Thermal decomposition study of the complexes was monitored by TG and DTG analyses under N(2) atmosphere. The decomposition course and steps were analyzed and the activation parameters of the nonisothermal decomposition are determined. The isolated metal chelates have been screened for their antimicrobial activities and the findings have been reported and discussed in relation to their structures. Hindawi Publishing Corporation 2008 2008-02-28 /pmc/articles/PMC2268950/ /pubmed/18364993 http://dx.doi.org/10.1155/2008/479897 Text en Copyright © 2008 Nouria A. Al-Awadi et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Al-Awadi, Nouria A. Shuaib, Nadia M. Abbas, Alaa El-Sherif, Ahmed A. El-Dissouky, Ali Al-Saleh, Esmaeil Synthesis, Characterization, and Biological Activity of N(1)-Methyl-2-(1H-1,2,3-Benzotriazol-1-y1)-3-Oxobutan- ethioamide Complexes with Some Divalent Metal (II) Ions |
title | Synthesis, Characterization, and Biological Activity of N(1)-Methyl-2-(1H-1,2,3-Benzotriazol-1-y1)-3-Oxobutan- ethioamide Complexes with Some Divalent Metal (II) Ions |
title_full | Synthesis, Characterization, and Biological Activity of N(1)-Methyl-2-(1H-1,2,3-Benzotriazol-1-y1)-3-Oxobutan- ethioamide Complexes with Some Divalent Metal (II) Ions |
title_fullStr | Synthesis, Characterization, and Biological Activity of N(1)-Methyl-2-(1H-1,2,3-Benzotriazol-1-y1)-3-Oxobutan- ethioamide Complexes with Some Divalent Metal (II) Ions |
title_full_unstemmed | Synthesis, Characterization, and Biological Activity of N(1)-Methyl-2-(1H-1,2,3-Benzotriazol-1-y1)-3-Oxobutan- ethioamide Complexes with Some Divalent Metal (II) Ions |
title_short | Synthesis, Characterization, and Biological Activity of N(1)-Methyl-2-(1H-1,2,3-Benzotriazol-1-y1)-3-Oxobutan- ethioamide Complexes with Some Divalent Metal (II) Ions |
title_sort | synthesis, characterization, and biological activity of n(1)-methyl-2-(1h-1,2,3-benzotriazol-1-y1)-3-oxobutan- ethioamide complexes with some divalent metal (ii) ions |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2268950/ https://www.ncbi.nlm.nih.gov/pubmed/18364993 http://dx.doi.org/10.1155/2008/479897 |
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