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Synthesis,spectroscopic study,X-ray diffraction,and comparative antimicrobial study of Schiff bases based on o-toluidine and their Co(II) complexes
Institution:1. Selvamm Arts and Science College, Namakkal, 637 003, Tamilnadu, India;2. Adiyamaan College of Engineering, Hosur, 635 209, Tamilnadu, India;3. Department of Physics, Periyar University, Salem, 636 011, Tamilnadu, India;1. Aryabhatta Centre for Nanoscience & Nanotechnology, Aryabhatta Knowledge University, Patna, 800001, India;2. Dept. of Zoology, A N College, Patna and Dept. of Education, Govt. of Bihar, India;1. Department of Chemistry, Faculty of Sciences, Aydin Adnan Menderes University, 09010, Aydin, Turkey;2. Department of Physics, Faculty of Sciences, Aydin Adnan Menderes University, 09010, Aydin, Turkey;3. Technical Sciences Vocational School, Gazi University, Ostim, Ankara, 06374, Turkey;1. Department of Engineering Chemistry, Andhra University, Visakhapatnam, India;2. Department of Chemistry, Adikavi Nannaya University, Rajahmundry, India;3. Department of Chemical Engineering, Andhra University, Visakhapatnam, India;4. Department of Chemistry, KGRL College, Bhimavaram, India;5. Department of Chemistry, P. R. Government College (A), Kakinada, 533001, A. P., India;6. Department of Engineering Physics, AUCE (A), Andhra University, Visakhapatnam, India;1. Department of Chemistry, Mashhad Branch, Islamic Azad University, Mashhad, Iran;2. Department of Chemistry, Quchan Branch, Islamic Azad University, Quchan, Iran;1. Department of Physics, Federal University of Health Sciences, Otukpo, Benue State, Nigeria;2. Operations Unit, Starsight Energy, Nigeria;3. Centre for Satellite Technology Development-NASRDA, Abuja, Nigeria;4. Department of Physics, Rivers State University, Port Harcourt, Rivers State, Nigeria
Abstract:Schiff bases are versatile compounds for the design of the ternary complex. An experiment has been made to synthesize two novel complexes of Co(II). Here, The primary ligand, L1 was prepared by the condensation reaction of o-toluidine with 3-formyl chromone or o-toluidine with 3- methylquinolinecarbaldehyde and the secondary ligand which was 8-Hydroxyquinoline. These potent complexes were prepared by condensation of primary and secondary ligands with Cobalt salt. The reaction was performed through the conventional reflux method. The newly synthesized chromone and quinoline derived novel compounds are proposed to have significant antimicrobial activity against selective strains of bacteria and fungi. This can be great opportunity for researchers and the use of biological applications of the synthesized novel compounds can be a part of unique field of research for the future to be focus. Chromone derivative has great biological diversity in the medicinal and pharmaceutical fields. Along with these compounds, quinoline derivatives also have antibacterial, and antifungal activities. The synthesized ligand and complex were characterized by elemental analysis, molecular weight determination, magnetic moment measurement, melting point determination, spectral analysis (IR, UV–Vis, 1H NMR, Mass, etc.), and X-ray diffraction. The synthesized complexes were paramagnetic and non-electrolytic in nature. The Uv–Vis, FTIR, NMR, and Mass spectra suggest the octahedral geometry of the complexes. The synthesized compounds were further evaluated for biological studies against selected bacterial and fungal strains. It has been observed that the antimicrobial activity of most of the complexes are better than that of ligands.
Keywords:Ternary complex  Schiff base  2-Aminopyridine  8-Hydroxyquinoline  Chromone  Quinoline  Biological studies  g  "}  {"#name":"keyword"  "$":{"id":"pc_1213pOvMzH"}  "$$":[{"#name":"text"  "_":"gram  ml"}  {"#name":"keyword"  "$":{"id":"pc_uoDUOgc82x"}  "$$":[{"#name":"text"  "_":"mililiter  mg"}  {"#name":"keyword"  "$":{"id":"pc_PCvH5rQlFL"}  "$$":[{"#name":"text"  "_":"miligram  Mol  wt  "}  {"#name":"keyword"  "$":{"id":"pc_vVi63BvHZD"}  "$$":[{"#name":"text"  "_":"molecular weight  Mol  cond  "}  {"#name":"keyword"  "$":{"id":"pc_unpEzxu2al"}  "$$":[{"#name":"text"  "_":"molecular conductance  Cal  "}  {"#name":"keyword"  "$":{"id":"pc_TRAY6aHFpa"}  "$$":[{"#name":"text"  "_":"calculated  nm"}  {"#name":"keyword"  "$":{"id":"pc_lerC1Yce22"}  "$$":[{"#name":"text"  "_":"nanometer  DMSO"}  {"#name":"keyword"  "$":{"id":"pc_9k1GObTBVr"}  "$$":[{"#name":"text"  "_":"dimethyl sulfoxide  DMF"}  {"#name":"keyword"  "$":{"id":"pc_9HmZhmymtV"}  "$$":[{"#name":"text"  "_":"dimethylformamide  Ppm"}  {"#name":"keyword"  "$":{"id":"pc_fE46CYrI0D"}  "$$":[{"#name":"text"  "_":"part per million
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