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Exploring the synthesis, of transition metal complexes derived from 5-nitrosalicyaldehyde benzoylhydrazone characterization and their antimicrobial activities

Author Affiliations

  • 1Federal University Dutsin-ma, Applied Chemistry, P.M.B 5001 Dutsin-ma, Katsina Nigeria
  • 2Federal University Dutsin-ma, Applied Chemistry, P.M.B 5001 Dutsin-ma, Katsina Nigeria

Res.J.chem.sci., Volume 13, Issue (3), Pages 27-32, October,18 (2023)

Abstract

Synthesis as well as Characterization of a Hydrazine derivative Schiff Base (L^) Derived from 5-Nitrosalicylaldehyde and Benzhydrazides, along with their transition divalent metal chelates of Ni, Cu, and Co. The complex ion were characterized using Melting Temperatures, FT-IR Spectrum Analysis, Magnetic Susceptibility, and UV-Vis Spectroscopy. These vibrant and stable ketimine and chelates remain undissolved in pure water but readily dissolve in organic solvents such as Dimethyl sulfoxide, acetone, and ethanol. The magnetic and spectral measurements suggest an octahedral geometry for the metal ions. The spectral data of the ligand displayed a prominent band at 1580c/m, confirming the presence of the imine group after synthesis. Interestingly, in the chelates, this peaks shifted to a higher spatial frequency, suggesting coordination of the imine nitrogen with the metal, thus establishing complexation through the N-atom of the imine moiety. The antimicrobial efficacy of the chelation compounds and ligating molecule was evaluated using the disc diffusion method against the bacterial isolates, namely Pseudomonas - aeruginosa, Enterobacter - cloacae, Klebsiella - pneumoniae, as well as Staphylococcus - aureus (G -ve and G +ve respectively), the fungi isolates, Aspergillus - niger as well as Phytopthera - infestans. Comparing the inhibitory effect of the analysis of the ligand (L1) and its respective chelate molecule demonstrated that the chelates displayed enhanced antimicrobial potency compared to the unbound ligand.

References

  1. Akbas, E., Celik, S., Ergan, E., & Levent, A. (2019)., Synthesis, characterization, quantum chemical studies and electrochemical performance of new 4, 7-dihydrotetrazolo [1, 5-a] pyrimidine derivatives., Journal of Chemical Sciences, 131, 1-10.
  2. Júnior, W. B., Alexandre-Moreira, M. S., Alves, M. A., Perez-Rebolledo, A., Parrilha, G. L., Castellano, E. E., ... & Beraldo, H. (2011)., Analgesic and anti-inflammatory activities of salicylaldehyde 2-chlorobenzoyl hydrazone (H2LASSBio-466), salicylaldehyde 4-chlorobenzoyl hydrazone (H2LASSBio-1064) and their zinc (II) complexes., Molecules, 16(8), 6902-6915.
  3. Özdemir, A., Turan-Zitouni, G., Asım Kaplancıklı, Z., Revial, G., Demirci, F., & İşcan, G. (2010)., Preparation of some pyrazoline derivatives and evaluation of their antifungal activities., Journal of Enzyme Inhibition and Medicinal Chemistry, 25(4), 565-571.
  4. Govindasami, T., Pandey, A., Palanivelu, N., & Pandey, A. (2011)., Synthesis, characterization and antibacterial activity of biologically important vanillin related hydrazone derivatives., international journal of organic chemistry, 1(03), 71.
  5. Savini, L., Chiasserini, L., Travagli, V., Pellerano, C., Novellino, E., Cosentino, S., & Pisano, M. B. (2004)., New α-(N)-heterocyclichydrazones: evaluation of anticancer, anti-HIV and antimicrobial activity., European journal of medicinal chemistry, 39(2), 113-122.
  6. Vicini, P., Incerti, M., La Colla, P., & Loddo, R. (2009). Anti-HIV evaluation of benzo [d] isothiazole hydrazones. European Journal of Medicinal Chemistry, 44(4), 1801-1807., undefined, undefined
  7. Lovejoy, D. B., & Richardson, D. R. (2002)., Novel “hybrid” iron chelators derived from aroylhydrazones and thiosemicarbazones demonstrate selective antiproliferative activity against tumor cells., Blood, The Journal of the American Society of Hematology, 100(2), 666-676.
  8. Nikolova-Mladenova, B. I., & Angelova, S. E. (2017)., Synthesis of 5-nitrosalicylaldehyde based hydrazones and DFT-calculations of their structure and reactivity., Bulg. Chem. Comm., 49, 800-806.
  9. Gürbüz, D., Çinarli, A., Tavman, A., & Tan, A. S. B. (2015)., Synthesis, characterization and antimicrobial activity of some transition metal complexes of N-(5-chloro-2-hydroxyphenyl)-3-methoxy-salicylaldimine., Bulletin of the Chemical Society of Ethiopia, 29(1), 63-74.
  10. Yusha’u, M., & Salisu, F. U. (2011)., Inhibition activity of detarium microcarpum extracts on some clinical bacterial isolates., Biological and Environmental Science Journal for the tropics, 8(4), 113-117.
  11. National Committee for Clinical Laboratory Standards (NCCLS). (2008)., Performance standards for Antimicrobial susceptibility testing, 9th informational supplements., Wayne, PA: National Committee for Clinical Laboratory Standards. M 100-59.
  12. Koley, M. K., Sivasubramanian, S. C., Varghese, B., Manoharan, P. T., & Koley, A. P. (2008)., Synthesis and characterization of two stable paramagnetic octahedral chromium (IV) complexes with dianionic tridentate SNO donor ligands and of a chromium (III) complex with a ONO donor ligand., Inorganica Chimica Acta, 361(5), 1485-1495.
  13. Shivakumar, K., Shashidhar, Vithal Reddy, P., & Halli, M. B. (2008)., Synthesis, spectral characterization and biological activity of benzofuran Schiff bases with Co (II), Ni (II), Cu (II), Zn (II), Cd (II) and Hg (II) complexes., Journal of Coordination Chemistry, 61(14), 2274-2287.