Abstract

A Mannich base ligand (L) was prepared by reacting 2-mercaptobenzimidazole, diphenylamine and benzaldehyde. This ligand (L) was further used for the preparation of four metal complexes with Co(II), Ni(II), Cu(II) and Zn(II) ions. The reactions were monitored by TLC. The synthesized compounds were structurally characterized using FTIR spectroscopy, UV-Visible spectroscopy, 1H- and 13C-NMR spectroscopy, ICP-OES/atomic absorption spectroscopy. It has been observed that the ligand (L) behaved in a monoanionic bidentate mode and the geometry of resulting complexes was tetrahedral. Conductivity analysis revealed their non-electrolytic nature. Antibacterial activity of the synthesized compounds was assessed through an agar well diffusion method against four strains of Gram-negative bacteria. L-Zn(II) complex showed best activity at all four concentrations against the four strains of Gram-negative bacteria. KEY WORDS: Metal complexes, Mannich bases, 2-Mercaptobenzimidazole, Antibacterial activity Bull. Chem. Soc. Ethiop. 2019, 33(3), 485-492.DOI: https://dx.doi.org/10.4314/bcse.v33i3.9

Highlights

  • Mannich base is a well known ligand obtained by the condensation of aldehydes, amines and active hydrogen substrates via Mannich reaction [1, 2]

  • The ligand (L) and its metal complexes were prepared by the general outlines given above in experimental section (Schemes 1 and 2)

  • Physical properties of ligand and its respective metal complexes are given in experimental section

Read more

Summary

Introduction

Mannich base is a well known ligand obtained by the condensation of aldehydes, amines and active hydrogen substrates via Mannich reaction [1, 2]. The present work includes the synthetic schemes for a Mannich base ligand (L) derived from 2-mercaptobenzimidazole and its transition metal complexes with Co(II), Ni(II), Cu(II) and Zn(II) ions. The resulting ligand solution was added drop wise in the respective solution of metal salt (0.5 mmol) and stirred for 5-6 h followed by evaporation/concentration.

Results
Conclusion
Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.