Co(II), Ni(II), and Cu(II) complexes of aroylhydrazone mixed with aspirin were synthesized and characterized by percentage metal analysis, infrared and electronic spectroscopy, melting point, solubility, molar conductance and room temperature magnetic moment measurements. Infrared spectra data revealed that the aspirin behaved as a bidentate ligand with coordination via carboxylate and carbonyl groups while the hydrazine coordinated via the azomethine nitrogen atom and carbonyl oxygen atom in the aroylhydrazone. The room temperature magnetic moment and electronic spectral data that the metal complexes possessed octahedral geometry. The molar conductance measurements of all the metal complexes in DMF indicated that they are non-electrolytes. The in vitro antimicrobial activities studies showed that the Cu(II) complex had the best activity against tested bacteria; Streptococcus spp, B. subtlis and vibro spp with inhibitory zones range of 2.0 - 6.0 mm, while the Ni(II) complex showed considerable activity against gram negative bacteria; Shigella spp with inhibitory zone of 10.0 mm suggesting its potential as an antimicrobial agent.
Published in | Science Journal of Chemistry (Volume 7, Issue 3) |
DOI | 10.11648/j.sjc.20190703.13 |
Page(s) | 67-71 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
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Copyright © The Author(s), 2019. Published by Science Publishing Group |
Antimicrobial, Aroylhydrazone (HL), Aspirin (HASA), Carboxylate, Azomethine
[1] | Baligar R. S., Revankar V. K. (2006) Coordination diversity of new mononucleating hydrazone in 3d metal Complexes: synthesis, characterization and structural studies. Journal of Serbian Chemical Society, 71 (12), 1301–1310. |
[2] | El-Halima B. D., Hanan F., Omar M. M., Gehad M. G. (2011) Synthesis, structural, thermal studies and biological activity of a tridentate schiff base ligand and their transition metal complexes. Spectrochemical Acta Part A, 78, 36-44. |
[3] | Gupta A. K., Pal1 R., Beniwal V. (2014) Novel dehydroacetic acid based hydrazine schiff’s base metal complexes of first transition series: synthesis and biological evaluation study. World Journal of Pharmacy and Pharmaceutical Sciences, 4 (1), 990-1008. |
[4] | Hania M. M. (2009) Synthesis and antibacterial activity of some transition metal complexes of oxime, semicarbazone and phenylhydrazone, E-journal of Chemistry, 6 (1), 508–514. |
[5] | Hollander, M. D. (1994) Gastrointestinal complications of non-steroidal anti-Inflammatory drugs: prophylactic and therapeutic strategies. American Journal of Medicine, 96: 274-281. |
[6] | Kamini J. D. (2015) Spectroscopy and structure of transition metal complexes of hydrazone derivatives. Journal of Pharmacy Research, 9 (4), 299-305. |
[7] | Köse, D. A., Hasan I., Hacali N. (2007) Synthesis and characterization of the nicotinamide-acetylsalicylato complexes of Co(II), Ni(II), Cu(II), and Zn(II). Hacettepe Journal of Biology & Chemistry, 35 (2) 123-128. |
[8] | Lawal A., Obaleye, J. A. (2005) Synthesis, characterization and antibacterial activity of aspirin and paracetamol-metal complexes. Journal of Biochemistry, 19, 9-15. |
[9] | Lee J. D. Concise Inorganic Chemistry. 5th edition. India: Blackwell Science Limited. 2005, 205-324. |
[10] | Leuner C., Dressmann J. (2002) Improving Drug Solubility for Oral Delivery Using Solid Dispersions. European Journal of Pharmacy: BioPharm, 54, 107–112. |
[11] | Mahal A., Abu-El-Halawa R., Zabin S. A., Ibrahim M., Kaimari A. T. (2015) Synthesis, characterization and antifungal activity of some metal complexes derived from quinoxaloylhydrazone. World Journal of Organic Chemistry, 3 (1), 1-8. |
[12] | Mohammed M. A., Mohammed S. J. (2012) Synthesis and characterization of Co(II), Ni(II), Cu(II), Zn(II) and Cd(II) complexes with aroylhydrazonemonoximes. Science Journal Article, 23 (4): 51-69. |
[13] | Mtrei R., Yadawa M., Patil, S. A. (1996) Synthesis of biologically active p-bis(amino-5- mercapto-1,2,4-triazol-3-yl) benzene and its schiff base: new class of bis-triazole. Orient Journal of Chemistry, 12, 101-102. |
[14] | Olanrewaju, A. A., Oni, T. I. Osowole, A. A. (2016) Synthesis, Characterization and Antioxidant Properties of Some Metal(II) Complexes of Mixed Drugs Vitamin Bx and Aspirin. Chemistry Research Journal, 2016, 1 (4), 90-96. |
[15] | Geary W. J. (1971) The use of conductivity measurements in organic solvents for the characterisation of coordination compounds. Coordination Chemistry Reviews, 7 (1), 81-122. |
[16] | Osowole A. A., Wakil S. M., Alao O. K. (2015) Inorganic synthesis, characterization and antimicrobial activity of some mixed trimethoprim-sulfamethoxazole metal drug complexes. World Applied Sciences Journal, 33 (2), 336-342. |
[17] | Padmini K., Jaya P., Divya M., Rohini P., Lohita M., Swetha, K., Kaladar P. (2013) A Review on Biological Importance of Hydrazones. International Journal of Pharma Research & Review, 2 (8), 43-58. |
[18] | Pouralimardan O., Chamayou A. C., Jniak C., Monfared H. H. (2007) Hydrazone Schiff base Manganese (II) Complexes: Synthesis, Crystal Structure and Catalytic Reactivity. Inorganica Chemica Acta, 360 (5), 1599-1608. |
[19] | Ajayeoba, T. A., Akinyele, O. F., Ayeni, A. O., Olawuni. I. J. (2019) Synthesis, Characterisation and Acetylcholinesterase Inhibition Activity of Nickel(II) and Copper(II) Complexes of 3-Hydroxybenzaldehyde-4-nitrobenzoic Acid Hydrazone. American Journal of Applied Chemistry. Vol. 7 (2), 64-71. |
APA Style
Olawale Folorunso Akinyele, Temitope Oluwatola Akinnusi, Temitope Adekunle Ajayeoba, Ayowole Olaolu Ayeni, Lateefah Moyosore Durosinmi. (2019). Synthesis, Characterization and Antimicrobial Activities of Cobalt(II), Nickel(II) and Copper(II) Complexes of Aroylhydrazone Mixed with Aspirin. Science Journal of Chemistry, 7(3), 67-71. https://doi.org/10.11648/j.sjc.20190703.13
ACS Style
Olawale Folorunso Akinyele; Temitope Oluwatola Akinnusi; Temitope Adekunle Ajayeoba; Ayowole Olaolu Ayeni; Lateefah Moyosore Durosinmi. Synthesis, Characterization and Antimicrobial Activities of Cobalt(II), Nickel(II) and Copper(II) Complexes of Aroylhydrazone Mixed with Aspirin. Sci. J. Chem. 2019, 7(3), 67-71. doi: 10.11648/j.sjc.20190703.13
AMA Style
Olawale Folorunso Akinyele, Temitope Oluwatola Akinnusi, Temitope Adekunle Ajayeoba, Ayowole Olaolu Ayeni, Lateefah Moyosore Durosinmi. Synthesis, Characterization and Antimicrobial Activities of Cobalt(II), Nickel(II) and Copper(II) Complexes of Aroylhydrazone Mixed with Aspirin. Sci J Chem. 2019;7(3):67-71. doi: 10.11648/j.sjc.20190703.13
@article{10.11648/j.sjc.20190703.13, author = {Olawale Folorunso Akinyele and Temitope Oluwatola Akinnusi and Temitope Adekunle Ajayeoba and Ayowole Olaolu Ayeni and Lateefah Moyosore Durosinmi}, title = {Synthesis, Characterization and Antimicrobial Activities of Cobalt(II), Nickel(II) and Copper(II) Complexes of Aroylhydrazone Mixed with Aspirin}, journal = {Science Journal of Chemistry}, volume = {7}, number = {3}, pages = {67-71}, doi = {10.11648/j.sjc.20190703.13}, url = {https://doi.org/10.11648/j.sjc.20190703.13}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.sjc.20190703.13}, abstract = {Co(II), Ni(II), and Cu(II) complexes of aroylhydrazone mixed with aspirin were synthesized and characterized by percentage metal analysis, infrared and electronic spectroscopy, melting point, solubility, molar conductance and room temperature magnetic moment measurements. Infrared spectra data revealed that the aspirin behaved as a bidentate ligand with coordination via carboxylate and carbonyl groups while the hydrazine coordinated via the azomethine nitrogen atom and carbonyl oxygen atom in the aroylhydrazone. The room temperature magnetic moment and electronic spectral data that the metal complexes possessed octahedral geometry. The molar conductance measurements of all the metal complexes in DMF indicated that they are non-electrolytes. The in vitro antimicrobial activities studies showed that the Cu(II) complex had the best activity against tested bacteria; Streptococcus spp, B. subtlis and vibro spp with inhibitory zones range of 2.0 - 6.0 mm, while the Ni(II) complex showed considerable activity against gram negative bacteria; Shigella spp with inhibitory zone of 10.0 mm suggesting its potential as an antimicrobial agent.}, year = {2019} }
TY - JOUR T1 - Synthesis, Characterization and Antimicrobial Activities of Cobalt(II), Nickel(II) and Copper(II) Complexes of Aroylhydrazone Mixed with Aspirin AU - Olawale Folorunso Akinyele AU - Temitope Oluwatola Akinnusi AU - Temitope Adekunle Ajayeoba AU - Ayowole Olaolu Ayeni AU - Lateefah Moyosore Durosinmi Y1 - 2019/09/17 PY - 2019 N1 - https://doi.org/10.11648/j.sjc.20190703.13 DO - 10.11648/j.sjc.20190703.13 T2 - Science Journal of Chemistry JF - Science Journal of Chemistry JO - Science Journal of Chemistry SP - 67 EP - 71 PB - Science Publishing Group SN - 2330-099X UR - https://doi.org/10.11648/j.sjc.20190703.13 AB - Co(II), Ni(II), and Cu(II) complexes of aroylhydrazone mixed with aspirin were synthesized and characterized by percentage metal analysis, infrared and electronic spectroscopy, melting point, solubility, molar conductance and room temperature magnetic moment measurements. Infrared spectra data revealed that the aspirin behaved as a bidentate ligand with coordination via carboxylate and carbonyl groups while the hydrazine coordinated via the azomethine nitrogen atom and carbonyl oxygen atom in the aroylhydrazone. The room temperature magnetic moment and electronic spectral data that the metal complexes possessed octahedral geometry. The molar conductance measurements of all the metal complexes in DMF indicated that they are non-electrolytes. The in vitro antimicrobial activities studies showed that the Cu(II) complex had the best activity against tested bacteria; Streptococcus spp, B. subtlis and vibro spp with inhibitory zones range of 2.0 - 6.0 mm, while the Ni(II) complex showed considerable activity against gram negative bacteria; Shigella spp with inhibitory zone of 10.0 mm suggesting its potential as an antimicrobial agent. VL - 7 IS - 3 ER -