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Kelode, S. R.
- Synthesis, Characterization and Thermal Studies of Co(II), Ni(II), Cu(II) and Zn(II) Metal Complexes derived from Bidentate thiazole Schiff base
Abstract Views :225 |
PDF Views:2
Authors
Affiliations
1 Department of Engg. Chemistry, Jagadambha College of Engineering and Technology, Yavatmal
1 Department of Engg. Chemistry, Jagadambha College of Engineering and Technology, Yavatmal
Source
Asian Journal of Research in Chemistry, Vol 6, No 7 (2013), Pagination: 702-704Abstract
A new series of Schiff base ligand was derived from the condensation of 2-hydroxy-5-chloro-3-nitro acetophenone and thiazole. The Schiff bases behaved as charge bidentade ligand. The ligand was characterized by elemental analysis and spectral methods. The coordinating ability of the ligand is investigated by preparing its metal complexes with Co(II), Ni(II), Cu(II) and Zn(II) have been prepared and characterized by elemental analysis, conductance measurements, molecular weight determinations, spectral and thermal studies. The synthesized products are coloured solids, soluble in DMF, DMSO and THF.Keywords
Schiff Base, Magnetic Susceptibility, Thermal
References
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- Patai S, The chemistry of carbon-Nitrogen double bond (John wiley and sons Ltd, London) 1970.
- Raziya S., Mohan S and Rao S., Indian J. Chem., 46B, 2007, 884.
- Kumar S., Dhar D. and Saxena P., J. Sci.and Indu.Research, 68, 2009, 181.
- Reji T., Devi S, Thomas K., Sreejalekshmi K., Manju S., Francis M.,.Philip S ,
- Bharathan A., and Rajasekharan K., Indian j. Chem., 47B, 2008, 1145.
- Aswar A., Bahad P.,.Pardhi A. and Bhave N., J. Poym. Mater. 5, 232 (1988).
- Pattan S.,.Ali M, Pattan J., Purohit S., Reddy V. and Nataraj B., Indian J. Chem., 45B, 2006, 1929.
- Khrustalev D., Suleimenova A. and Fazylov S., Russian J. App. chem., 81(5), 2008, 900
- Maradiya H., and Patel V., J. Fibers and poly., 3(1), 2002, 43.
- Furniss B., Hannaford A., Smith P. and Tatchell A., Vogel’s practical organic chemistry 5 thEd. (Logman Scientific Technical, John Wiley and Sons), (1989).
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- Pietikainen P. and Haikarainen A. J. Mole. Catalysis., 180, 2002, 59.
- Kidwai M., Poddar P. and Singhal K., Indian J. Chem., 48B, 2009, 59.
- Sonwane S., Srivastava S. and Srivastava S., Indian J. Chem., 47B, 2008 633.
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- Maurya R., Antony D., Gopinathan S., Puranic V., Tavale S.and Gopinathan C., Bull. Chem. Soc. Jpn., 68, 1995, 2847.
- Boghaei D. and Mohebi S. J. Tetrahedron, 58, 2002, 5357.
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- Thermal and Microbial Evolution of Co(II), Ni(II), Cu(II) and Zn(II) Metal Complexes derived from thiazole Schiff base
Abstract Views :335 |
PDF Views:2
in DMF, DMSO and THF.
Authors
Affiliations
1 Department of Engg. Chemistry, Jagadambha College of Engineering and Technology, Yavatmal
1 Department of Engg. Chemistry, Jagadambha College of Engineering and Technology, Yavatmal
Source
Asian Journal of Research in Chemistry, Vol 6, No 8 (2013), Pagination: 713-715Abstract
A new series of Schiff base ligand was derived from the condensation of 2-hydroxy-5-chloro-3-nitro acetophenone and thiazole. The Schiff bases behaved as charge bidentade ligand. The ligand was characterized by elemental analysis and spectral methods. The coordinating ability of the ligand is investigated by preparing its metal complexes with Co(II), Ni(II), Cu(II) and Zn(II) have been prepared and characterized by elemental analysis, conductance measurements, molecular weight determinations, spectral and thermal studies. The Schiff base and their metal complexes have been evaluated for their antibacterial activities The synthesized products are coloured solids, solublein DMF, DMSO and THF.
Keywords
Schiff Base, Magnetic Susceptibility, ThermalReferences
- Aghera V. K. and Parsania P. H., J. Sci. and Ind. Res., 67, 2008, 1083.
- Patai S, The chemistry of carbon-Nitrogen double bond (John wiley and sons Ltd, London) 1970.
- Raziya S., Mohan S and Rao S., Indian J. Chem., 46B, 2007, 884.
- Kumar S., Dhar D. and Saxena P., J. Sci.and Indu.Research, 68, 2009, 181.
- Reji T., Devi S, Thomas K., Sreejalekshmi K., Manju S., Francis M.,.Philip S , Bharathan A., and Rajasekharan K., Indian j. Chem., 47B, 2008, 1145.
- Aswar A., Bahad P.,.Pardhi A. and Bhave N., J. Poym. Mater. 5, 232 (1988).
- Pattan S.,.Ali M, Pattan J., Purohit S., Reddy V. and Nataraj B., Indian J. Chem., 45B, 2006, 1929.
- Khrustalev D., Suleimenova A. and Fazylov S., Russian J. App. chem., 81(5), 2008, 900
- Maradiya H., and Patel V., J. Fibers and poly., 3(1), 2002, 43.
- Furniss B., Hannaford A., Smith P. and Tatchell A., Vogel’s practical organic chemistry 5 thEd. (Logman Scientific Technical, John Wiley and Sons), (1989).
- Sadigova S., Magerramov A. and Allakhverdiev M., Russian J. Org. chem., 81(5), 2008, 900.
- Vogel AI, “A Text book of quantitative inorganic chemistry”3thEd., (ELBS,London,1961).
- Campbell E. and Nguyen S., J. Tetrahedron, 42, 2001, 1221.
- Pietikainen P. and Haikarainen A. J. Mole. Catalysis., 180, 2002, 59.
- Kidwai M., Poddar P. and Singhal K., Indian J. Chem., 48B, 2009, 59.
- Sonwane S., Srivastava S. and Srivastava S., Indian J. Chem., 47B, 2008 633.
- Patel K. and Mehata A., E. J. Chem., 3(13), 2006, 267.
- Maurya R., Antony D., Gopinathan S., Puranic V., Tavale S.and Gopinathan C., Bull. Chem. Soc. Jpn., 68, 1995, 2847.
- Boghaei D. and Mohebi S. J. Tetrahedron, 58, 2002, 5357.
- Mallikarjun K., E. J. Chem., 1(2), 2004, 105.
- Horowitz H. and Metzger G., Anal. Chem., 35, 1963, 1464.
- Broido A., J. Polym. Sci. Part, A2, 1964, 1761.
- Sutariya B., Mohan S., Sambasiva S. and Rao S., Indian j. Chem., 46B, 2007, 884
- Baluja S., Solanki A. and Kachhadia N., J. Iranian Chem. Soc., 3(4), 2006, 312.
- Venkatesh P., Asian J. Pharm. Hea. Sci., 1(1), 2011, 8.