Synthesis, spectral characterization, catalytic and antibacterial activity of macrocyclic CuII compounds

Transition Metal Chemistry

Volumn 32, Issue 4, 2007, Pages 507-513

  Reddy, P Muralidhar ^a   Prasad, Adapa V S S ^a   Ravinder, Vadde ^a  

^a KAKATIYA UNIVERSITY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ACRYLICS; BACTERIA; CATALYST ACTIVITY; KETONES; SPECTRUM ANALYSIS; SYNTHESIS (CHEMICAL);

ANTIBACTERIAL ACTIVITY; ASCORBIC ACIDS; OCTAHEDRAL GEOMETRY; SPECTRAL CHARACTERIZATION;

COPPER COMPOUNDS;

EID: 34249047072     PISSN: 03404285     EISSN: None     Source Type: Journal    
DOI: 10.1007/s11243-007-0205-7     Document Type: Article

References (36)

1. G. Hu, Z.D. Zhang, L. Hu and J.M. Song, Transition Met. Chem., 30, 856 (2005).
2. M. Rosignoli, P.V. Bernhardt, G.A. Lawrence and M. Maeder, J. Chem. Soc, Dalton Trans, 323 (1997).
3. M.S. Niasari and A. Amiri, J. Mol. Cat. A, 235, 114 (2005).
4. D.P. Singh, R. Kumar and P. Tyagi, Transition Met. Chem., 31, 970 (2006).
5. M. Shakir, O.S.M. Nasman and S.P. Varkey, Polyhedron, 15, 309 (1996).
6. O.S.M. Nasman, Synth. Read. Inorg. Met. Org. Chem., 31, 1433 (2001).
7. M. Shakir, H. Chishti, Y. Azim and N. Begum, Synth. React. Inorg. Met. Org. Chem., 34, 809 (2004).
8. T.A. Khan, S. Tabassum, Y. Azim and M. Shakir, Synth. React. Inorg. Met. Org. Chem., 34, 1305 (2004).
9. M. Shakir, H.T.N. Chishti and P. Chingsubam, Spectrochim. Acta. A, 64, 512 (2006).
10. M. Shakir, Y. Azim, H.T.N. Chishti and S. Parveen, Spectrochim. Acta (A), 65, 490 (2006).
11. M. Ashok, V. Ravinder and A.V.S.S. Prasad, Transition Met. Chem., 32, 23 (2007).
12. H. Schumann, V. Ravindar, L. Meltser, W. Baidossai, Y. Sasson and J. Slum, J. Mol. Cat. A, 118, 55 (1997).
13. V. Ravindar, H. Hemling, H. Schumann, W. Baidossai and J. Blum, J. Mol. Cat. A, 85, 1603 (1993).
14. V. Ravinder, V. Narasaiah, A.B. Rao and P.M. Reddy, J. Ind. Council. Chem., 24, 1 (2006).
15. MR. Esteban and C.N. Ho, Microchem. J., 56, 122 (1997).
16. Vogel's, Text Book of Quantitative Chemical Analysis, 6th edit., Pearson Edu., India, 2004.
17. H. Okawa, J. Nishio, M. Ohoba, M. Tadokoro, N. Matumast sumoto, M. Koikawa, S. Kaida and D.E. Fenton, Inorg. Chem., 32, 2949 (1993).
18. N. Bharati, S.S. Sharma, F. Naqvi and A. Azam, Bioinorg. Med. Chem., 11, 2923 (2003).
19. C. Hamciuc, E. Hamciuc, M. Bruma, M. Klapper and T. Pakula, Polymer Bull., 47, 1 (2001).
20. L. Mishra and K.K. Upadhyay, Ind. J. Chem., 31, 169 (1992).
21. H. Keypour, S. Salehzadeh, R.G. Pritchard and R.V. Parish, Molecules, 6, 909 (2001).
22. C.M. Mikulski, L. Mattucci, Y. Smith, T.B. Tran and N.M. Karayannis, Inorg. Chim. Acta, 80, 127 (1983).
23. S. Chandra and S. Gupta, J. Ind. Chem. Soc. 1087, (2005).
24. W.J. Geary, Coord. Chem. Rev., 7, 81 (1971).
25. L. Banci, A. Bencini, C. Benelli, D. Gatteschi and C. Zanchini, Struct. Bond., 52, 38 (1982).
26. J.R. Allan and T.M. Veitch, J. Therm. Anal., 27, 3 (1983).
27. A.T. Colak, M. Tumer and S. Serin, Transit. Met. Chem., 25, 200 (2000).
28. S.N. Choi, E.R. Menzil and J.R. Walson, J. Inorg. Nucl. Chem., 39, 417 (1977).
29. T.P.T. Cushine and A.J. Lamb, Inter. J. Antimicrob. Agents, 26, 343 (2005).
30. M. Maluc, J.M. Bastide and A. Biancard, Inter. J. Antimicrob. Agents, 25, 321 (2005).
31. P.E. Strizhak, A.B. Basylchuk, I. Demjanchyk, F. Fecher, F.W. Schneiderb and A.F. Munsterb, Chem. Phys., 2, 4721 (2000).
32. A.M. Lambeir, H.B. Dunford and M.A. Pickard, Euro. J. Biochem., 163, 123 (1987).
33. M. Noroozifar, M.K. Motlagh and A.R. Farahmanda, Acta Chim. Slov., 51, 717 (2004).
34. M. Noroozifar and M.K. Motlagh, Turk. J. Chem., 27, 717 (2003).
35. G.S. Fresenius, J. Anal. Chem., 265, 5 (1947).
36. J.C. Deutsch, Anal. Biochem., 255, 1 (1998).