Synthesis and Microbial Activity Determination of Synthesized Products of Iron(II) and Nickel (II) Complexes of Schiff Base Using 2-Aminoaniline and 2-Thiosylaniline


Authors : Esonwune, Anacletus Anayochukwu; Ugochukwu B. Amadi

Volume/Issue : Volume 10 - 2025, Issue 3 - March


Google Scholar : https://tinyurl.com/2rj3k2dv

Scribd : https://tinyurl.com/mr2tepuv

DOI : https://doi.org/10.38124/ijisrt/25mar1363

Google Scholar

Note : A published paper may take 4-5 working days from the publication date to appear in PlumX Metrics, Semantic Scholar, and ResearchGate.

Note : Google Scholar may take 15 to 20 days to display the article.


Abstract : Four Metal complexes of Iron(II) and Nickel(II): FeNcplx, FeScplx, NiNcplx and NiScplx were synthesized in this study. Molar conductivity, elemental composition, color, melting point, and % yield were among the physical and analytical parameters measured for ligands and complexes. Analyzers for FT-IR, UV-VIS, and MS were used for characterization. The FT-IR results indicated the synthetic path rout of the functional groups of the compounds. Deprotonation and the use of phenolic OH in bond formation provide evidence of ligands losing their -OH bond to complexation. There were more peaks in the UV-VIS spectra of 2-aminoaniline complexes and Schiff bases due to the increased number of chromophoric groups. The MS of the results confirmed the proposed structures of the reaction as evident to m/z values indicating molecular weight of the ligands and complexes. The studies of Antibacterial (Salmonella enterica, Escherichia coli, Staphylococcus aureus and Bacillus subtilis) and Antifugal (Aspergillus flavus, Rhizopus stolonifer, Fusarium moniliforme, and Fusarium solani) activities with respect to the synthesized compounds showed that the complexes have greater efficacy in antifungal and antibacterial activities than with the ligands going from the area of inhibition zones. Further research can be done to incorporate these complexed synthesized into antibiotics and other drugs, as evident to antimicrobial efficacy.

Keywords : Schiff Base, Ligands, 2-Aminoaniline, 2-Thiosylaniline, 2-Hydroxynapthaldehye, Complexation.

References :

  1. Sahil, B., (2018). Spectrophotometer-Principle, Components, Working and Applications. https//paramedicsworld.com/tag/principle-of-spectr (Accessed February 25, 2020).
  2. Whitten, K. W., Davis, R. E., Peek, M. L. and Stanley, G. G. (2004). General Chemistry. 7th Ed. Thompson Leaving, London, Pp. 220-226.
  3. Ankur, C. (2017). The Principle of Ultra Violet (UV) Spectrophotometer. www.https://medium.com (Accessed February 24, 2020).
  4. Sagar, A. (2020). Mass spectrometry (MS). Principle, Working, Instrumentation, Steps, Application online microbiology Notes. https://microbenotes.com (Retrieved March 4, 2020).
  5. Ogwuegbu, M. O. C. and Ehirim, A. I. (2010). Application of Coordination Chemistry in Medicine and Biochemical Systems. Madonna International Journal Research, 3(1):95-113.
  6. Sebastian, M. (2010). Transition Metal Complexes of Quinoxaline Based Schiff base ligands: Synthesis, Characterization and Catalytic Activity Study. Unpublished Ph.D Thesis submitted to the Cochin University of Science and Technology.
  7. Anas Haruna (2016). Synthesis and Antibacterial Studies of some Transition Metal Complexes Derived from 1-(2-hydroxyphenyl) (Iminomethyl) naphthalene-2-0l MSc dissertation submitted to Department of Pure and Industrial Chemistry, Faculty of Science, Bayero University, Kano.
  8. Basavaraj M., Dinnimoth, Pooja Gowda and Anwesh Naik (2023). Development of Organomettalic Compounds of Schiff bases with Diverse Application. International Journal of Pharmacy and Pharmaceutical Sciences, 15(6):1-15.
  9. Sadia, A. D., Farhana, A., Mol.Saddam, H., Mol.Nuruzzaman, K., Zakaria, C. M., Mol.Kudirat, E. Z. and Mol.Moshin, A. (2018). A short Review on Chemistry of Schiff Base Metal Complexes and their Catalytic Application. Internal Journal of Chemical Studies, 6(3):2859-2866.
  10. Garnovskii, A. D., Vasilchenko, I. S., Garnovskii, D. A. and Kharisov, B. I. (2009). Molecular Design of Monocuclear Complexes of Acyclic Schiff-Base Ligands. Journal of Coordination Chemistry 62:151-204.
  11. Kiran, S., Yogender, K., Parveshi, P., Chetan, S. and Kamal, R. A. (2017). Antimicrobial, Spectral and Thermal Studies of Divalent Cobalt, Nickel, Copper and Zinc Complexes with Tirazole Schiff Bases. King Saad University. Arabian Journal of Chemistry. 10:5978-5987.
  12. Srivastava, R. (2017). Theoretical Insight into the Medicinal World of Organometallics. Macro Versus Nano Recent Prog Organomet Chem. 2017(1):3-13.
  13. Hameed, A., Al-Rashida, M., Uroos, M., Ali, S. A. and Khan, K. M. (2016). Schiff Bases in Medicinal Chemistry: A Potent Review (2010-2015). Expert Opin Therapy Patent, 27:63-67.
  14. Da-Silva, C.M., da Silva, D. L., Modolo, L. V., Alves, R. B., de Resende, M. A., Martins, C. O. B. and Fatima, A. (2011). Schiff Bases: A Short Review of Antimicrobial Activities. Journal of Advanced Research, 2:1-8.
  15. Felix, S. N. (2016). Bis(salicylidene) ethylenediamine-metal complexes: From Structure to Biological Activity. Journal Analytical and Pharmaceutical Research, 3(6):00076.
  16. Singh, H. L. and Varshney, A. K. (2006). Synthetic, Structural and Biochemical Studies of Organotrin (iv) with Schiff Bases having Nitrogen and Sulphur Donor Ligands. Bioinorganic Chemicals Application. 23:2-45.
  17. Chandhary, N. K. (2013). In vitro Antibacterial Studies of some Transition Metal Complexes of Schiff base Derived from 2-aminophenol and from-2-carboldehyde, Archives of Applied Science Research, 5(6): 227-231.
  18. Ezenweke, L.O., Ojiako, E. N., Esonwune, A. A. and Olugbue, V. U. (2021). Chemical Synthesis and Microbial Evaluation of Iron (II) and Cobalt (II) complexes of Schiff base Derives from β-hydroxy naphthalene-1-carbaldehyde using 2-Aminoaniline and 2-Hydroxyaniline as the Aniline Di-substituents. International Journal of Science and Research (IJSR) 10(8):1-13.
  19. Tanim Jabid Hossain (2024). Methods for Screening and Evaluating of Antimicrobial Activity: A Review of Protocols, Advantages and Limitations European Journal of Microbiological and Immunology 14(2):97-115.
  20. Daver, M. and Sajjad, M. (2001). Novel Unsymmetrical Tetradentate Schiff Base Complexes of Cobalt(II) and Palledium (II) with N2O2 donor sets. Journal of Chemical Research(s) 2001:224-226.
  21. Linus, O. E., Eugene, N. O., Anacletus, A. E.and Alisa, C. O. (2021). Synthesis, Characterization and Antimicrobiological activity studies of Cobalt(II) and Nickel (II) Complexes Derived from 2-hydroxynaphthalene-1-carbaldehyde using 2-thiosylaniline and 2-Aminoaniline as a co-schiff bases IOSR. Journal of Applied Chemistry (IOSR-JAC), 14(8):57-62.
  22. Vivekananda, D. B. and Mruthyunjayaswamy, B. H. M. (2013). “Synthesis, Characterization and Antimicrobial Activity Studies of some Transition Metal Complexes derived from 3-chloro-N-[CIE) – (2-hydroxyphenyl) methylene] – 6-methoxy-1-benzothiophene-2-carbohydrazide”. The Scientific World Journal  2013 (Article ID 457629): 1-13.
  23. Deshpande V.S., Shah S.N.N., Deshpande M.M., Seema I.H. and Kalkarni P.A (2013). Synthesis and Antimicrobial Evaluation of Schiff Bases Derived from 2-amino-4, 6-dimethyl-Denzothiozole with 2-Hydroxy-naphthalene-I-Carbaldehyde, 3-Methylthiophene-2-Carbaldehyde and their complexes, Lutl.J. of Pharmaceutical and Chemical Sciences 2(2): 801-807.
  24. Dayaneshwar, S.W. and Sandip, S.C. 92017). Synthsis, Characterization and Antimicrobial Activities of Mixed Ligand Complexes of Trnasition Metals using 2-aminophenol and 2-Chloroaniline as Ligands. Asian J. Research Chem. 10(5):639-645.
  25. Onianwo, P. (2021). Methods of Analysis. ISI Analytical, Surulere, Lagos. Pp. 1-5.
  26. Usharami, M., Akila, E. and Rajavel, R. (2013). Derivation of N, N, O Donor Sites of Organic Schiff Base Ligand Based on 2-Hydroxynaphthalene-1-Carbaldehyde and their Cu(II) and Co(II) Complexes. International Journal of Advanced Scientific and Technical Research, 5(3):198-201.
  27. Thangavel, T., Rajendran, J., Rubiga, M., Ekambaram, A. and Rangappan, R. (2017). Exploration of New Mononuclear Schiff Base Cu (II), Ni(II) and Co(II) Complexes Using Physicochemical Methods. IOSR Journal of Applied Chemistry, 10(8):46-53.
  28. Sumathi, R. B. and Halli, M. B. (2014). Metal (II) Complexes Derived from Naphthofuran-2-Carbohydrazide and Diacetylmonoxime Schiff Bases: Synthesis, Spectroscopic, Electrochemical and Biological Investigation. Hiundawi Publication and Corporation of Bioinorganic Chemistry and Applications 2014 (Article ID 942162):1-11.
  29. Akila, E., Usharani, M. and Rajavel, R. (2013). Potentially Bioactive Schiff Base Transition Metal(II) complexes as Selective DNA Binding Cleavage. In vitro  Antimicrobial and in vitro Antioxidant Agents. International Journal of Medicine and Pharmaceutical Sciences, 3(2):95-112.
  30. Imadul, SK., Scuvendu, I., Sutapa, B. D., Sudeshna, C., Akhil, H. P. and Animeshi, P. (2016). Synthesis, Characterization and Biological Activity of Nickel(II) and palladium (III) Complex with Pyrrolidine Dithiocarbonate (DDTC). Advances in Chemistry, 2016 (Article ID 4676524):1-6.
  31. Mendham, J., Denney, R. C., Barnes, J. D. and Thomas, M. J. K. (2000). Vogels Text Book of Quantitative Chemical Analysis. 6th Ed. Pearson Educational Limited, Edinburgh Gate. England. Pp. 649-650.
  32. Eugene, A. T. (2019). Coherent and Quantum Optics. Institute of Physics of the National Academy of Science. Research Gate, Ukraine. P. 1.
  33. Kalaiselvan, S. (2019). UV-VIS Research Gate Answers Chemistry SNS College of Technology, Skills and Expertise. M. Kumarasamy College of Engineering, India, P. 1.  
  34. Ayman, H. A., Hassan, A. M., Hoani, A. G., Bassam, H. M. and Ahmed, M. F. (2016). Nickel (II) Oxaloyldihydrazone Complexes, Characterization, Indirect Band Gap Energy and Antimicrobial Evaluation. Cogent Chemistry Open Access. https://doi.org/10.1080/2331 2009.2016.1142820.
  35. Savithri K., Vassntha Kumar B.C., Vivek H.K. and Revanosiddappa H.D. (2018). Synthesis and Characterization of Cobact (III) and Copper (II) Complexed of 2-(€-(6-Fluorobenzo [d] Thiozol -2-Ylimino)Methy)-4 Chlorophenol. DNA Binding and Nuclear Studies-SOD and Antimicrobial Actiivities. Intl. J. of Spectroscopy 2018:1-15.
  36. Kouris, E., Kalogiannis, S., Peridh, F., Turel, I. and Psomas, G. (2016). Cobalt(II) complexes of Sparfloxalin: Characterization, Structure, Antimicrobial Activity and Interaction with DNA and Albunins. Journal of Inorganic Biochemistry, 163:18-27.
  37. Faridul, I., Md.Amran, H., NurMostag, S., Hridika, T. B., Md.Alamgir, K., Mohammed, J. K. and Romel, M. (2015). Synthesis, Characterization and Antimicrobial Activity Studies of Ni(II) complexes with Pyridine as a Ligand. Journal of Chemistry. 2015 (Article ID 525239):1-8.
  38. Nageh, A., Tamer, N., Heba, A. and Elsherif, Z. J. (2017). Chemical and Pharmaceutical Research, 9(3):135-140.
  39. Yong, S. S., Lee, J. I. and Kang D. H. (2023). TiO2-based photocatalyst  Generated Reactive Oxygen Species Cause Cell Membrane Disruption of Staphylococcus arueus  and Escherichia coli 0157:H7. Food Microbial. 2023; 109:104119.10.1016/j. FM.2022.104119.
  40. Nemah, S. M. H. (2018). Preparation and Characterization, Chromatography, Antimicrobial Activities of some Metal Complexes of 1-(2-hydroxy-4-Nitrophenyl azo)-2-Naphthol. Biochemical Cellular Archeology, 18(1):901-906.

Four Metal complexes of Iron(II) and Nickel(II): FeNcplx, FeScplx, NiNcplx and NiScplx were synthesized in this study. Molar conductivity, elemental composition, color, melting point, and % yield were among the physical and analytical parameters measured for ligands and complexes. Analyzers for FT-IR, UV-VIS, and MS were used for characterization. The FT-IR results indicated the synthetic path rout of the functional groups of the compounds. Deprotonation and the use of phenolic OH in bond formation provide evidence of ligands losing their -OH bond to complexation. There were more peaks in the UV-VIS spectra of 2-aminoaniline complexes and Schiff bases due to the increased number of chromophoric groups. The MS of the results confirmed the proposed structures of the reaction as evident to m/z values indicating molecular weight of the ligands and complexes. The studies of Antibacterial (Salmonella enterica, Escherichia coli, Staphylococcus aureus and Bacillus subtilis) and Antifugal (Aspergillus flavus, Rhizopus stolonifer, Fusarium moniliforme, and Fusarium solani) activities with respect to the synthesized compounds showed that the complexes have greater efficacy in antifungal and antibacterial activities than with the ligands going from the area of inhibition zones. Further research can be done to incorporate these complexed synthesized into antibiotics and other drugs, as evident to antimicrobial efficacy.

Keywords : Schiff Base, Ligands, 2-Aminoaniline, 2-Thiosylaniline, 2-Hydroxynapthaldehye, Complexation.

Never miss an update from Papermashup

Get notified about the latest tutorials and downloads.

Subscribe by Email

Get alerts directly into your inbox after each post and stay updated.
Subscribe
OR

Subscribe by RSS

Add our RSS to your feedreader to get regular updates from us.
Subscribe