JOURNAL BROWSE
Search
Advanced SearchSearch Tips
Synthesis and Characterization of Transition Metal Complexes with Benzimidazolyl-2-hydrazones of o-anisaldehyde and Furfural
facebook(new window)  Pirnt(new window) E-mail(new window) Excel Download
 Title & Authors
Synthesis and Characterization of Transition Metal Complexes with Benzimidazolyl-2-hydrazones of o-anisaldehyde and Furfural
Mohapatra, R.K.; Mishra, U.K.; Mishra, S.K.; Mahapatra, A.; Dash, D.C.;
  PDF(new window)
 Abstract
A series of complexes of the type [], where L=2-(o-anisylidene-2'-imino) amino benzimidazole (AIAB) and 2-(furfurylidene imino) amino benzimidazole (FIAB), M=Cu(II), Co(II), Ni(II) and Zn(II), have been synthesized and characterized on the basis of elemental analysis, thermal analysis, molar conductivity, magnetic moment, electronic, infrared, -NMR spectral studies. The results are in consistent with bidentate chelation of ligand with azomethine nitrogen and ring nitrogen donors. All these Schiff bases and their complexes have also been screened for their antibacterial (Bacillus subtilis, Bacillus stearothermophilus, Escherichia coli and Salmonella typhi) and antifungal activities (Aspergillus niger and Aspergillus flavus).
 Keywords
Benzimidazolyl-2-hydrazones;o-anisaldehyde;Furfural and Transition metal complexes;
 Language
English
 Cited by
1.
Synthesis, Characterization, and Photophysical Studies of Some Novel Ruthenium(II) Polypyridine Complexes Derived from Benzothiazolyl hydrazones, International Journal of Inorganic Chemistry, 2013, 2013, 1  crossref(new windwow)
2.
Synthesis, crystal structure and luminescence properties of acenaphthene benzohydrazide based ligand and its zinc(II) complex, Journal of Molecular Structure, 2017, 1128, 195  crossref(new windwow)
3.
Synthesis, Spectroscopic Characterization, and Biological Evaluation Studies of 5-Bromo-3-(((hydroxy-2-methylquinolin-7-yl)methylene)hydrazono)indolin-2-one and Its Metal (II) Complexes, Bioinorganic Chemistry and Applications, 2014, 2014, 1  crossref(new windwow)
 References
1.
Katsuki, T. Coord. Chem. Rev. 1995, 140, 189. crossref(new window)

2.
Di Bella, S. Chem. Soc. Rev. 2001, 30, 355. crossref(new window)

3.
Cogan, D. A.; Liu, G. C.; Kim, K. J.; Backes, B. J.; Ellman, J. A. J. Am. Chem. Soc. 1998, 120, 8011. crossref(new window)

4.
Pandeya, S. N.; Sriram, D.; Nath, G.; De Clercq, E. Eur. J. Pharma. Soc. 1999, 9, 25. crossref(new window)

5.
Raper, E. S. Coord. Chem. Rev. 1996, 153, 199. crossref(new window)

6.
Sridhar, S. K.; Pandeya, S. N.; Stables, J. P.; Ramesh, A. Eur. J. Pharm. Sci. 2002, 16, 129. crossref(new window)

7.
Vicini, P.; Zani, F.; Cozzini, P.; Doytchinova, I. Eur. J. Med. Chem. 2002, 37, 553. crossref(new window)

8.
Kocyigit-Kaymakcioglu, B.; Rollas, S. Farmaco 2002, 57, 595. crossref(new window)

9.
Ragavendran, J. V.; Sriram, D.; Patel, S. K.; Reddy, I. V.; Bharathwajan, N.; Stables, J.; Yogeeswari, P. Eur. J. Med. Chem. 2007, 42, 146. crossref(new window)

10.
Rollas, S.; Gulerman, N.; Erdeniz, H. Farmaco 2002, 57, 171. crossref(new window)

11.
Carcelli, M.; Mazza, P.; Pelizi, C.; Zani, F. J. Inorg. Biochem. 1995, 57, 43. crossref(new window)

12.
Johnson, D. K.; Murphy, T. B.; Rose, N. J.; Goodwin, W. H.; Pickart, L. Inorg. Chim. Acta 1982, 67, 159. crossref(new window)

13.
Ranford, J. D.; Vittal, J. J.; Wang, Y. M. Inorg. Chem. 1998, 37, 1226. crossref(new window)

14.
Buss, J. L.; Greene, B. T.; Turner, J.; Torti, F. M.; Torti, S. V. Curr. Top. Med. Chem. 2004, 4, 1623. crossref(new window)

15.
Dash, D. C.; Mahapatra, A.; Pathjoshi, S. B.; Mishra, U. K.; Naik, S. K. J. Indian Chem. Soc. 2006, 83, 782.

16.
Dash, D. C.; Mahapatra, A.; Jena, P.; Naik, S. K.; Mishra, U. K. J. Indian Chem. Soc. 2007, 84, 1092.

17.
Dash, D. C.; Mahapatra, A.; Mohapatra, R. K.; Ghosh, S.; Naik, P. Indian J. Chem. 2008, 47A, 1009.

18.
Dash, D. C.; Mohapatra, R. K.; Ghosh, S.; Naik, P. J. Korean Chem. Soc. 2008, 52(5), 468. crossref(new window)

19.
Dash, D. C.; Mohapatra, R. K.; Ghosh, S.; Naik, P. J. Indian Chem. Soc. 2009, 86, 121.

20.
Mohapatra, R. K. J. Indian Chem. Soc. 2010, 87, 1251.

21.
Mohapatra, R. K.; Dash, D. C. J. Korean Chem. Soc. 2010, 54(4), 395. crossref(new window)

22.
Dash, D. C.; Mahapatra, A.; Naik, P.; Mohapatra, R. K.; Naik, S. K. J. Korean Chem. Soc. 2011, 55(3), 412. crossref(new window)

23.
Katz, L. J. Am. Chem. Soc. 1951, 73, 4007. crossref(new window)

24.
Vogel, A. I. A text book of Quantitative Inorganic Analysis, 3rd ed.; Longman and ELBS: 1969.

25.
Kalsi, P. S. Spectroscopy of Organic Compounds, New Age International limited; New Delhi, 1998; p 77.

26.
Carlin, R. L. Transition Metal Chemistry; Marcel Dekker Inc.: New York, 1965.

27.
Lever, A. B. P. Inorganic Electronic Spectroscopy; Elsevier Publication: New York, 1968.

28.
Ali, M. A.; Livingstone, S. E. Coord. Chem. Rev. 1974, 13, 101. crossref(new window)

29.
Bustoup, O.; Jorgensen, C. K. Acta Chem. Scand. 1957, 11, 1223. crossref(new window)

30.
Sacconi, L. Trans. Metal Chem. 1968, 4, 199.

31.
Ballhausen, C. J.; Liehr, A. D. J. Am. Chem. Soc. 1959, 81, 538. crossref(new window)

32.
Balhausen, C. J. An Introduction to Ligand Field; McGraw Hill: New York, 1962

33.
Chohan, Z. H.; Pervez, H.; Kausar, S.; Supuran, C. T. Synth. React. Inorg. Met.-Org. Chem. 2002, 3, 529.

34.
Chohan, Z. H.; Pervez, H.; Rauf, A.; Supuran, C. T. Metal-Based Drugs 2002, 8, 42.

35.
Chohan, Z. H.; Scozzafava, A.; Supuran, C. T. J. Enzyme Inhib. Med. Chem. 2003, 18, 259. crossref(new window)

36.
Chohan, Z. H.; Hassan, M. U.; Khan, K. M.; Supuran, C. T. J. Enzyme Inhib. Med. Chem. 2005, 20, 181.