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Microwave-assisted Synthesis, Characterization and Antibacterial Study of Schiff Base Metal (II) Complexes Derived from 2-Aminophenol and P-chlorobenzaldehyde

Received: 12 September 2026     Accepted: 24 September 2026     Published: 29 October 2026
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Abstract

The growing resistance of microorganisms to existing antibiotics has increased the need for new and more effective antimicrobial agents. In this study, Schiff base ligand was synthesized from 2-aminophenol and p-chlorobenzaldehyde, and its cobalt (II) and lead (II) complexes. The compounds were characterized using melting point determination, solubility tests, Ultraviolet–visible (UV-Vis), Fourier Transform Infrared spectroscopy (FTIR), Elemental analysis, and Magnetic susceptibility measurements. The FTIR spectrum of the ligand showed a characteristic band at 1610 cm-1 due to the formation of azomethine (C=N) group, confirming Schiff base formation. In the metal (II) complexes, this band shifted to lower frequencies, 1638 and 1612 cm-1 indicating coordination of the azomethine nitrogen to the metal ions. The O–H stretching band at 3429 cm-1 for ligand shifted to 3257 and 3047 cm-1 upon complexation, suggesting involvement of the phenolic oxygen atom. UV–visible and magnetic data indicated an octahedral geometry around Pb(II) and tetrahedral around Co(II). Elemental analysis revealed the expected molecular compositions of the prepared Schiff base ligand. Antibacterial studies using Staphylococcus aureus and Escherichia coli showed that the metal complexes displayed higher inhibitory activity against the tested bacterial strains compared with the free ligand. This enhancement suggests that coordination with metal ions increases the biological effectiveness of the Schiff base. Overall, the results indicated formation and characterization of the Schiff base ligand and its cobalt (II) and lead (II) complexes, demonstrating their potential as promising antimicrobial agents.

Published in Modern Chemistry (Volume 14, Issue 4)
DOI 10.11648/j.mc.20261404.11
Page(s) 109-115
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.

Copyright

Copyright © The Author(s), 2026. Published by Science Publishing Group

Keywords

Schiff Base, Metal (II), 2-aminophenol, Antibacterial, Spectroscopy

References
[1] Adebayo, T. M., Oladipo, A. A., & Ogunyemi, A. O. (2023). Spectroscopic and biological evaluation of transition-metal Schiff base complexes derived from substituted salicylaldehydes. Journal of Molecular Structure, 1298, 136222.
[2] Ajibulu, K. E., Okoronkwo, A. E., Owolabi, J. B., Oyetayo, V. O., Adeyemi, E. O and Pii, B. T. (2025). Metal Complexes of Schiff Base Derived from Ethylenediamine, Nitro and Chlorobenzaldehyde; Synthesis, Characterization, Biological and Toxicological Study. Applied Sciences Research Periodicals, Vol. 3, No. 1 pp. 50-60.
[3] Ajibulu, K. E., Okoronkwo, A. E., Owolabi, J. B. and Oyetayo, V. O. (2023). Synthesis, Characterization, antimicrobial and Toxicological Study of Mn(II), Ni(II) Complexes of Tridentate Ligand Derived from ethylenediamine, Chlorobenzalde-hyde and aminobenzophenone. International Journal of Science and innovative Research - Novus, 04(01), 010001481JESIR.
[4] Ajibulu, K. E., Okoronkwo, A. E., Owolabi, J. B., and Oyetayo, V. O. (2021). Synthesis, Characterization and Antibacterial Activity Of Schiff Base, n, n1- Bis(4-Nitrobenzylidene) Ethylenediamine, Metal (II) Complexes. World Journal of Pharmacy and Pharmaceutical Sciences, 10 (9), 2059-2072.
[5] Alshaheri, A. A., Tahir, M. I., Rahman, M. B., Begum, T., Saleh, T. A. (2017). Synthesis, characterisation and catalytic activity of dithiocarbazate Schiff base complexes in oxidation of cyclohexane. Journal of Molecular Liquids. 240: 486-496.
[6] Venkatesh G, Vennila P, Kaya S, Ahmed SB, Sumathi P, Siva V, Rajendran P, Kamal C. (2024): Synthesis and Spectroscopic Characterization of Schiff Base Metal Complexes, Biological Activity, and Molecular Docking Studies. ACS Omega. 9(7): 8123-8138.
[7] Anita, R., Manoj, K., Rajshree, K. and Hardeep, S.T. (2015). Schiff bases as an antimicrobial agent: A review. Journal of Biological and Chemical Sciences, 2 (1), 62-9.
[8] Biplab, B. (2022). A Short Review on the Diverse Interactions in Metal-Organic Complexes: From Covalent to Non-Covalent. International Journal of Multidisciplinary, 7(5), 181-191.
[9] Constantinos, G. E., Vassilios, N., Catherine, R., Anastasios, T., Spyros, p, p., and Constantina, p. (2010). Mononuclear and Dinuclear Manganese(II) Complexes from the Use of Methyl (2-pyridyl) Ketone Oxime. Bioinorganic Chemistry and Application, 2010: 960571.
[10] Chandra, S., & Kumar, U. (2004). Spectral and biological studies of nickel (II) and copper (II) complexes with Schiff bases. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 60(1-2), 2461-2468.
[11] Desalegn, T., T. (2023). Synthesis, Characterization and Biological Activities of Schiff Bases and Their Transition Metal Complexes. World Journal of Applied Chemistry, 8(2): 22-33.
[12] Desai, P. S. and D. V. Parekh, D. V. (2021). Synthesis, characterization and biological screening of novel metal (II) complexes of 2-{[2-(5-Benzoyl-1 H -benzotriazol-1-yl)-2- oxoethyl] amino}-5-bromobenzoid,” Asian J. Chem., 2021.
[13] Ekennia, A. C., Onwudiwe, D.C., Osowole, A. A., Okpareke, O. C., Olubiyi, O. O. & Lane, J. R. (2019). Coordination compounds 0f heterocyclic bases: synthesis, characterization, computational and biological studies. Research on chemical intermediates, 45(3), 1169-1205.
[14] Ejidike, I. P, Mtunzi, F. M., Klink, M. J. (2019). Spectroscopic, XRD, in vitro anti-oxidant, antifungal and antibacterial studies of heterocyclic Schiff base Nickel (II) complexes bearing anions. In: Ramasami P, Gupta Bhowon M, Jhaumeer LS, Li K, Wah H (eds.). Chemistry for a clean and healthy planet. ICPAC-2018, Springer, Cham, Switzerland, 2019, 283-305.
[15] Ejidike, I. P., Ajibade, P. A. (2017). Synthesis, spectroscopic, antibacterial and free radical scavenging studies of Cu(II), Ni(II), Zn(II) and Co(II) complexes of 4, 4’-{ethane-1, 2- diylbis [nitrile (1E) eth-1-yl-1-ylidene]} dibenzene 1, 3-diol Schiff base. J Pharm Sci Res, 2017; 9(7): 593-600.
[16] Fahmi, N., Shrivastava, S., Meena, R., Joshi, S. C., Singh, R. V. (2013). Microwave assisted synthesis, spectroscopic characterization and biological aspects of some new chromium (III) complexes derived from N O donor Schiff bases. New Journal of Chemistry, 37(5): 1445-1453.
[17] Festus, S. F., Adesoji, A. O. (2019). Synthesis, Characterization, Thermogravimetric and Antioxidant Studies of New Cu(II), Fe(II), Mn(II), Cu(II), Zn(II), Co(II) and Ni(II) Complexes with Benzoic acid and 4, 4, 4-Trifluoro-1-(2-naphthyl)-1, 3-butanedione. International Journal of Chemistry; Vol. 11, No. 1; 2019.
[18] Gehad, G. M., Mohamed, M. O., and Ahmed, M. H. (2006). Metal Complexes of Schiff Bases: Preparation, Characterization, and Biological Activity. Turkish Journal of Chemistry 30 (3): 361-382.
[19] Jingdong., Ziru, L., and Xiuyan, W. (2023). Two novel lead (II) coordination complexes incorporating phenanthroline derivate: Synthesis and characterization, Main Group Metal Chemistry, 46: 20228045.
[20] Kargar, H., Fallah-Mehrjardi, M., Behjatmanesh-Ardakani, R., Munawar, K., Ashfaq, M., Tahir, M. (2021). Synthesis, spectral characterization, SC-XRD, HSA, DFT and catalytic activity of a dioxidomolybdenum complex with aminosalicyl-hydrazone Schiff base ligand: An experimental and theoretical approach. Polyhedron. 208: 115428.
[21] Lennard, B., RoyAerts, W., Sereina, R. (2022). Improving the IR spectra of alignment algorithm with Spectra deconvolution and combination Raman or VCD Spectroscopy. Phys chem chem phy., 22: 25(3): 2063-2074.
[22] Lever, A. P. (2001). Inorganic electronic spectroscopy (2nd ed.). Elsevier.
[23] Mohamed, G. G., Omar, M. M., Moustafa, B. S., AbdEl-Halim, H. F., Farag, N. A. (2022). Spectroscopic investigation, thermal, molecular structure, antimicrobial and anticancer activity with modelling studies of some metal complexes derived from isatin Schiff base ligand. Inorganic Chemistry Communications. 141: 109606.
[24] Mahmoud, W. H., Omar, M. M., Ahmed, Y. M., & Mohamed, G. G. (2020). Transition metal complexes of Schiff base ligand based on 4, 6-diacetyl resorcinol. Applied Organometallic Chemistry, 34 (4), 1-20.
[25] Nakomoto, K. (2009). Infrared and Raman Spectra of inorganic and coordination compounds (6th ed.). John Wiley & Sons.
[26] Ommenya, F. K. Nyawade, E. A. Andala, D. M. and Kinyua, J. (2020). Synthesis, Characterization and Antibacterial Activity of Schiff Base, 4-Chloro-2-{(E)-[(4 Fluoro phenyl) imino] methyl}phenol Metal (II) Complexes. Journal of Chemistry, Volume 2020.
[27] Osowole, A. A. & Festus, C. (2015). Synthesis, Characterization, Antimicrobial and Antioxidant Activities of Some Heteroleptic Metal (II) Complexes of 3-{[(Pyrimidin-2- yl) Imino] Methyl}Napthalen-2-ol. Journal of Chemical, Biological and Physical Sciences Section A, 6(1), 080-089.
[28] Patel, R. N., Singh, A., & Pandeya, K. B. (2012). Antimicrobial activity of cobalt (II) Schiff base complexes. Applied Organometallic Chemistry, 26(5), 238-243.
[29] Prakash, A. Singh, B. K. Bhojak, N and Adhikari, D. (2010). “Synthesis and characterization of bioactive zinc (II) and cadmium (II) complexes with new Schiff bases derived from 4- nitrobenzaldehyde and acetophenone with ethylenediamine,” Spectrochim. Acta -Part A Mol. Biomol. Spectrosc., 2010.
[30] Racheal, O. A., Ikechukwu, P. E., Hadley, S. C. (2023). Schiff base metal complexes as a dual antioxidant and antimicrobial agents. Journal of Applied Pharmaceutical Science, 13(03), 132-140.
[31] Ravinderpal, K. S., and Satya, P. (2019). Metal Complexes in Medicine: An Overview and Update from Drug Design Perspective. Cancer Therapy & Oncology International Journal, 2019; 14: 1-8.
[32] Raman, N., Sakthivel, A., & Thangaraja, C. (2013). DNA interaction and antimicrobial studies of Schiff base complexes. Journal of Molecular Structure, 1035, 398-405.
[33] Raman, N, Raja, Y. P., Kulandaisamy, (2001). A. Synthesis and characterization of Cu(II), Ni(II), Mn(II), Zn(II) and VO(II) Schiff base complexes derived from ophenylenediamine and acetoacetanilide. J Chem Sci, 113(3): 183-9.
[34] Shadia, A., E., and Ahmed, M. El., Islam, M. E., Mohamed, M. A. (2024). Palladium (II), platinum (II), and silver (I) complexes with 3-acetylcoumarin benzoylhydrazone Schiff base: Synthesis, characterization, biomolecular interactions, cytotoxic activity, and computational studies. RSC Adv., 2024, 14, 19512-19527.
[35] Sivasubramania, P., Nallamohamed, H., Rafik, R., Sathya, R., & Davoodbasha, M. (2023). Synthesis and Characterization of Novel Schiff bases Derived from 2-butyl-4-chloro imidazole for the enhancemed Antimicrobial Property. Appl. Biochem Biotecnol, 195(1): 253-263.
[36] Sunjuk, M., Al-Najjar, L., Shtaiwi, M., El-Eswed, B., Sweidan, K., Bernhardt, P., Zalloum, H., Al-Essa, L. (2023). Metal Complexes of Schiff Bases Prepared from Quinoline-3- Carbohydrazide with 2-Nitrobenzaldehyde, 2-Chlorobenzaldehyde and 2, 4- Dihydroxybenzaldehyde: Structure and Biological Activity. Inorganics, 2023, 11, 412.
[37] Singh, R., Kumar, D., & Verma, P. (2024). FTIR and UV-Visible spectral characterization of cobalt (II) and nickel (II) Schiff base complexes derived from o-aminophenol derivatives. Inorganic Chemistry Communications, 158, 111689.
[38] Wara, A. A. (2011). Transition Metal Complexes and their application in drugs and cosmetic - A Review, J Chem Pharm Res, 3(4): 951-95.
[39] Yang, X., Zhuang, X., Huang, Y., Jiang, J., Tian, H., Wu D. (2015). Nitrogen enriched hierarchically porous carbon materials fabricated by graphene aerogel templated Schiff-base chemistry for high performance electrochemical capacitors. Polymer Chemistry. 6(7): 1088 1095.
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    Ajibulu, K. E., Pii, B. T., Adebiyi, V. I., Nasiru, R. A. (2026). Microwave-assisted Synthesis, Characterization and Antibacterial Study of Schiff Base Metal (II) Complexes Derived from 2-Aminophenol and P-chlorobenzaldehyde. Modern Chemistry, 14(4), 109-115. https://doi.org/10.11648/j.mc.20261404.11

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    ACS Style

    Ajibulu, K. E.; Pii, B. T.; Adebiyi, V. I.; Nasiru, R. A. Microwave-assisted Synthesis, Characterization and Antibacterial Study of Schiff Base Metal (II) Complexes Derived from 2-Aminophenol and P-chlorobenzaldehyde. Mod. Chem. 2026, 14(4), 109-115. doi: 10.11648/j.mc.20261404.11

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    AMA Style

    Ajibulu KE, Pii BT, Adebiyi VI, Nasiru RA. Microwave-assisted Synthesis, Characterization and Antibacterial Study of Schiff Base Metal (II) Complexes Derived from 2-Aminophenol and P-chlorobenzaldehyde. Mod Chem. 2026;14(4):109-115. doi: 10.11648/j.mc.20261404.11

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  • @article{10.11648/j.mc.20261404.11,
      author = {Kehinde Ezekiel Ajibulu and Barizomdu Tina Pii and Victoria Ibukun Adebiyi and Rashidat Adebukola Nasiru},
      title = {Microwave-assisted Synthesis, Characterization and Antibacterial Study of Schiff Base Metal (II) Complexes Derived from 2-Aminophenol and P-chlorobenzaldehyde},
      journal = {Modern Chemistry},
      volume = {14},
      number = {4},
      pages = {109-115},
      doi = {10.11648/j.mc.20261404.11},
      url = {https://doi.org/10.11648/j.mc.20261404.11},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.mc.20261404.11},
      abstract = {The growing resistance of microorganisms to existing antibiotics has increased the need for new and more effective antimicrobial agents. In this study, Schiff base ligand was synthesized from 2-aminophenol and p-chlorobenzaldehyde, and its cobalt (II) and lead (II) complexes. The compounds were characterized using melting point determination, solubility tests, Ultraviolet–visible (UV-Vis), Fourier Transform Infrared spectroscopy (FTIR), Elemental analysis, and Magnetic susceptibility measurements. The FTIR spectrum of the ligand showed a characteristic band at 1610 cm-1 due to the formation of azomethine (C=N) group, confirming Schiff base formation. In the metal (II) complexes, this band shifted to lower frequencies, 1638 and 1612 cm-1 indicating coordination of the azomethine nitrogen to the metal ions. The O–H stretching band at 3429 cm-1 for ligand shifted to 3257 and 3047 cm-1 upon complexation, suggesting involvement of the phenolic oxygen atom. UV–visible and magnetic data indicated an octahedral geometry around Pb(II) and tetrahedral around Co(II). Elemental analysis revealed the expected molecular compositions of the prepared Schiff base ligand. Antibacterial studies using Staphylococcus aureus and Escherichia coli showed that the metal complexes displayed higher inhibitory activity against the tested bacterial strains compared with the free ligand. This enhancement suggests that coordination with metal ions increases the biological effectiveness of the Schiff base. Overall, the results indicated formation and characterization of the Schiff base ligand and its cobalt (II) and lead (II) complexes, demonstrating their potential as promising antimicrobial agents.},
     year = {2026}
    }
    

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  • TY  - JOUR
    T1  - Microwave-assisted Synthesis, Characterization and Antibacterial Study of Schiff Base Metal (II) Complexes Derived from 2-Aminophenol and P-chlorobenzaldehyde
    AU  - Kehinde Ezekiel Ajibulu
    AU  - Barizomdu Tina Pii
    AU  - Victoria Ibukun Adebiyi
    AU  - Rashidat Adebukola Nasiru
    Y1  - 2026/10/29
    PY  - 2026
    N1  - https://doi.org/10.11648/j.mc.20261404.11
    DO  - 10.11648/j.mc.20261404.11
    T2  - Modern Chemistry
    JF  - Modern Chemistry
    JO  - Modern Chemistry
    SP  - 109
    EP  - 115
    PB  - Science Publishing Group
    SN  - 2329-180X
    UR  - https://doi.org/10.11648/j.mc.20261404.11
    AB  - The growing resistance of microorganisms to existing antibiotics has increased the need for new and more effective antimicrobial agents. In this study, Schiff base ligand was synthesized from 2-aminophenol and p-chlorobenzaldehyde, and its cobalt (II) and lead (II) complexes. The compounds were characterized using melting point determination, solubility tests, Ultraviolet–visible (UV-Vis), Fourier Transform Infrared spectroscopy (FTIR), Elemental analysis, and Magnetic susceptibility measurements. The FTIR spectrum of the ligand showed a characteristic band at 1610 cm-1 due to the formation of azomethine (C=N) group, confirming Schiff base formation. In the metal (II) complexes, this band shifted to lower frequencies, 1638 and 1612 cm-1 indicating coordination of the azomethine nitrogen to the metal ions. The O–H stretching band at 3429 cm-1 for ligand shifted to 3257 and 3047 cm-1 upon complexation, suggesting involvement of the phenolic oxygen atom. UV–visible and magnetic data indicated an octahedral geometry around Pb(II) and tetrahedral around Co(II). Elemental analysis revealed the expected molecular compositions of the prepared Schiff base ligand. Antibacterial studies using Staphylococcus aureus and Escherichia coli showed that the metal complexes displayed higher inhibitory activity against the tested bacterial strains compared with the free ligand. This enhancement suggests that coordination with metal ions increases the biological effectiveness of the Schiff base. Overall, the results indicated formation and characterization of the Schiff base ligand and its cobalt (II) and lead (II) complexes, demonstrating their potential as promising antimicrobial agents.
    VL  - 14
    IS  - 4
    ER  - 

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Author Information
  • Department of Chemical Sciences, Bamidele Olumilua University of Education, Science and Technology, Ikere Ekiti, Nigeria

  • Department of Chemical Sciences, Bamidele Olumilua University of Education, Science and Technology, Ikere Ekiti, Nigeria

  • Department of Chemistry, Durban University of Technology, Durban, South Africa

  • Department of Chemical Sciences, Bamidele Olumilua University of Education, Science and Technology, Ikere Ekiti, Nigeria

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