Synthesis, Characterization, and Antimicrobial Activities of Coordination Compounds of Aspartic Acid
Coordination compounds of aspartic acid were synthesized in basic and acidic media, with metal ligand M : L stoichiometric ratio 1 : 2. The complexes were characterized using infrared, electronic and magnetic susceptibility measurements, and mass spectrometry. Antimicrobial activity of the compounds...
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doaj-0e62a0ec1db94d95a5e15deeb6819e3f2020-11-24T21:40:50ZengHindawi LimitedJournal of Chemistry2090-90632090-90712016-01-01201610.1155/2016/73170157317015Synthesis, Characterization, and Antimicrobial Activities of Coordination Compounds of Aspartic AcidT. O. Aiyelabola0D. A. Isabirye1E. O. Akinkunmi2O. A. Ogunkunle3I. A. O. Ojo4Department of Chemistry, Obafemi Awolowo University, Ife Central, Ile-Ife 220282, Osun State, NigeriaDepartment of Chemistry NWU, Mafikeng Campus, Private Bag X2046, Mmabatho 2735, South AfricaDepartment of Pharmaceutics, Obafemi Awolowo University, Ife Central, Ile-Ife 220282, Osun State, NigeriaDepartment of Chemistry, Obafemi Awolowo University, Ife Central, Ile-Ife 220282, Osun State, NigeriaDepartment of Chemistry, Obafemi Awolowo University, Ife Central, Ile-Ife 220282, Osun State, NigeriaCoordination compounds of aspartic acid were synthesized in basic and acidic media, with metal ligand M : L stoichiometric ratio 1 : 2. The complexes were characterized using infrared, electronic and magnetic susceptibility measurements, and mass spectrometry. Antimicrobial activity of the compounds was determined against three Gram-positive and three Gram-negative bacteria and one fungus. The results obtained indicated that the availability of donor atoms used for coordination was a function of the pH of the solution in which the reaction was carried out. This resulted in varying geometrical structures for the complexes. The compounds exhibited a broad spectrum of activity and in some cases better activity than the standard.http://dx.doi.org/10.1155/2016/7317015 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
T. O. Aiyelabola D. A. Isabirye E. O. Akinkunmi O. A. Ogunkunle I. A. O. Ojo |
spellingShingle |
T. O. Aiyelabola D. A. Isabirye E. O. Akinkunmi O. A. Ogunkunle I. A. O. Ojo Synthesis, Characterization, and Antimicrobial Activities of Coordination Compounds of Aspartic Acid Journal of Chemistry |
author_facet |
T. O. Aiyelabola D. A. Isabirye E. O. Akinkunmi O. A. Ogunkunle I. A. O. Ojo |
author_sort |
T. O. Aiyelabola |
title |
Synthesis, Characterization, and Antimicrobial Activities of Coordination Compounds of Aspartic Acid |
title_short |
Synthesis, Characterization, and Antimicrobial Activities of Coordination Compounds of Aspartic Acid |
title_full |
Synthesis, Characterization, and Antimicrobial Activities of Coordination Compounds of Aspartic Acid |
title_fullStr |
Synthesis, Characterization, and Antimicrobial Activities of Coordination Compounds of Aspartic Acid |
title_full_unstemmed |
Synthesis, Characterization, and Antimicrobial Activities of Coordination Compounds of Aspartic Acid |
title_sort |
synthesis, characterization, and antimicrobial activities of coordination compounds of aspartic acid |
publisher |
Hindawi Limited |
series |
Journal of Chemistry |
issn |
2090-9063 2090-9071 |
publishDate |
2016-01-01 |
description |
Coordination compounds of aspartic acid were synthesized in basic and acidic media, with metal ligand M : L stoichiometric ratio 1 : 2. The complexes were characterized using infrared, electronic and magnetic susceptibility measurements, and mass spectrometry. Antimicrobial activity of the compounds was determined against three Gram-positive and three Gram-negative bacteria and one fungus. The results obtained indicated that the availability of donor atoms used for coordination was a function of the pH of the solution in which the reaction was carried out. This resulted in varying geometrical structures for the complexes. The compounds exhibited a broad spectrum of activity and in some cases better activity than the standard. |
url |
http://dx.doi.org/10.1155/2016/7317015 |
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