ISSN

0974-4150 (Online)
0974-4169 (Print)


Author(s): Udaysinha Patil, Mustapha Mandewale, Bapu Thorat, Aarti Nagarsekar, Ramesh Yamgar

Email(s): iycmustapha@gmail.com

DOI: 10.5958/0974-4150.2016.00064.X   

Address: Udaysinha Patil1, Mustapha Mandewale1*, Bapu Thorat1, Aarti Nagarsekar1, Ramesh Yamgar2
1P.G. and Research Laboratory, Department of Chemistry, Government of Maharashtra, Ismail Yusuf College of Arts, Science and Commerce, Jogeshwari (East) Mumbai-400 060, India.
2Department of Chemistry, Chikitsak Samuha’s Patkar-Varde College of Arts, Science and Commerce, Goregaon (West), Mumbai 400 062, India.
*Corresponding Author

Published In:   Volume - 9,      Issue - 9,     Year - 2016


ABSTRACT:
A series of tetrahydrosalophen Schiff bases have been prepared from the reaction of two equivalents of salicylaldehyde with one equivalent o-phenylenediamine derivatives followed by reduction with NaBH4. The Co (II), Ni (II), Cu (II) and Zn (II) complexes of these ligands have been prepared. All the synthesized ligands and metal complexes were characterized by IR, 1H and 13C-NMR, MS, XRD, TGA, UV-Visible, Fluorescence and elemental analysis. The Preliminary results of antituberculosis study showed that the salophen schiff bases 2a-2b demonstrated very good antituberculosis activity while the tetrahydrosalophen schiff bases 3a-3i showed moderate activity. Among the tested metal complexes 4a was found to be most active with minimum inhibitory concentration (MIC) of 6.25 µg/ml against Mycobacterium tuberculosis (H37 RV strain) ATCC No- 27294.


Cite this article:
Udaysinha Patil, Mustapha Mandewale, Bapu Thorat, Aarti Nagarsekar, Ramesh Yamgar. Transition Metal Tetrahydro-Salophen Type Complexes: Synthesis, Characterization and Antitubercular Studies. Asian J. Research Chem. 2016; 9(9): 425-434. doi: 10.5958/0974-4150.2016.00064.X

Cite(Electronic):
Udaysinha Patil, Mustapha Mandewale, Bapu Thorat, Aarti Nagarsekar, Ramesh Yamgar. Transition Metal Tetrahydro-Salophen Type Complexes: Synthesis, Characterization and Antitubercular Studies. Asian J. Research Chem. 2016; 9(9): 425-434. doi: 10.5958/0974-4150.2016.00064.X   Available on: https://ajrconline.org/AbstractView.aspx?PID=2016-9-9-4


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