Structures, redox behavior, antibacterial activity and correlation with electronic structure of the complexes of nickel triad with 3-(2-(alkylthio) phenylazo)-2,4-pentanedione

Inorganica Chimica Acta

Volumn 370, Issue 1, 2011, Pages 175-186

  Paira, Mrinal Kanti ^a   Mondal, Tapan Kumar ^a   Ojha, Durbadal ^a   Slawin, Alexandra M Z ^b   Tiekink, Edward R T ^c   Samanta, Amalesh ^a   Sinha, Chittaranjan ^a  

^a JADAVPUR UNIVERSITY   (India)

^b UNIVERSITY OF ST ANDREWS   (United Kingdom)

^c UNIVERSITY OF MALAYA   (Malaysia)

Author keywords

3 (2 (Alkylthio)phenylazo) 2,4 pentanedione; Antibacterial activity; DFT computation; Group 10 metals; Redox; Structure

Indexed keywords

BACTERIOLOGY; CHELATION; ELECTRON SPIN RESONANCE SPECTROSCOPY; ELECTRONIC STRUCTURE; ESCHERICHIA COLI; NICKEL COMPOUNDS; PALLADIUM COMPOUNDS; SALMONELLA; SINGLE CRYSTALS; STAPHYLOCOCCUS AUREUS; STRUCTURE (COMPOSITION); SYNTHESIS (CHEMICAL);

3-(2-(ALKYLTHIO)PHENYLAZO)-2,4-PENTANEDIONE; ANTI-BACTERIAL ACTIVITY; DFT COMPUTATIONS; ELECTRONIC CONFIGURATION; MINIMUM INHIBITORY CONCENTRATION; PSEUDOMONAS AERUGINOSA; REDOX; SINGLE CRYSTAL X-RAY DIFFRACTION;

PLATINUM COMPOUNDS;

EID: 79954614823     PISSN: 00201693     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ica.2011.01.049     Document Type: Article

References (61)

1. W.Y. Wong, S.H. Cheung, S.M. Lee, and S.Y. Leung J. Organomet. Chem. 596 2000 36
2. L. Carlucci, G. Ciani, D.M. Proserpio, and S. Rizzato New. J. Chem. 27 2003 483
3. T. Akasaka, T. Mutai, J. Otsuki, and K. Araki J. Chem. Soc., Dalton Trans. 2003 1537
4. F. Casalbani, Q.G. Mulazzani, C.D. Clark, M.Z. Hoffman, P.L. Orizondo, M.W. Perkovic, and D.P. Rillema Inorg. Chem. 93 1998 205
5. V.W.-W. Yan, V.C.-Y. Lau, K.-K. Cheung, J. Chem. Soc., Chem. Commun. (1995) 259.
6. S. Frantz, J. Fiedler, I. Hartenbach, T. Schleid, and W. Kaim J. Organomet. Chem. 689 2004 3031
7. B.K. Ghosh, and A. Chakravorty Coord. Chem. Rev. 95 1989 239
8. B.K. Santra, G.A. Thakur, P. Ghosh, A. Pramanik, and G.K. Lahiri Inorg. Chem. 35 1996 3050
9. A.C. Cope, and R.W. Siekman J. Am. Chem. Soc. 87 1965 3272
10. S. Ganguly, S. Chattopadhyay, C. Sinha, A. Chakravorty, Inorg. Chem. 39 (2000) 2954 (and references therein).
11. R. Aharyya, F. Basuli, R.Z. Wang, T.C. Mak, S. Bhattacharya, Inorg. Chem. 43 (2004) 704 (and references therein).
12. A.H. Velders, K. van der Schilden, A.C.G. Hotze, J. Reedijk, H. Kooijman, A.L. Spek, J. Chem. Soc., Dalton Trans. (2004) 448.
13. T.K. Misra, T.K. Das, C. Sinha, P. Ghosh, and C.K. Pal Inorg. Chem. 37 1998 167
14. S. Senapati, U.S. Ray, P.K. Santra, C. Sinha, J.D. Woolins, and A.M.Z. Slawin Polyhedron 21 2002 753
15. D. Patra, J.L. Pratihar, B. Shee, P. Pattanayak, and S. Chattopadhyay Polyhedron 25 2006 2637
16. B. Adhikary, S. Liu, and C.R. Lucas Inorg. Chem. 32 1993 5957
17. K. Pramanik, S. Karmakar, S.B. Choudhury, and A. Chakravorty Inorg. Chem. 36 1997 3562
18. E.I. Solomon, R.K. Szilagyi, S.D. George, and L. Basumallick Chem. Rev. 104 2004 419
19. Y.F. Yuan, J.T. Wang, M.C. Gimeno, A. Laguna, and P.G. Jones Inorg. Chim. Acta 324 2001 309
20. R. Balamurigan, M. Palaniandavar, R.S. Gopalan, and G.U. Kulkarni Inorg. Chim. Acta 357 2004 919
21. H.V. Patel, and P.S. Fernandes Indian J. Chem., Sect. B 28 2 1989 167
22. L. Mishra, A.K. Yadaw, S. Srivastava, and P.A. Bahadur New J. Chem. 24 2000 505
23. L. Mishra, A.K. Yadaw, R.S. Phadke, C.S. Choi, and K. Araki Met.-Based Drugs 8 2001 65
24. P. Sharma, A. Kumar, P. Pandey, and N. Rane Indian J. Chem., Sect. B 43 2004 1320
25. S.R. Gadzhieva, T.M. Mursalov, K.T. Makhmudov, and F.M. Chyragov Russ. J. Coord. Chem. 32 2006 304
26. J. Marten, W. Seichter, E. Weber, and U. Boehme J. Phys. Org. Chem. 20 2007 716
27. K. Krishnankutty, P. Sayudevi, and M.B. Ummathur J. Indian Chem. Soc. 85 2008 48
28. S.F. Tayyari, R.E. Sammelson, F.R. Tayyari, H. Rahemi, and M. Ebrahimi J. Mol. Struct. 920 2009 301
29. S. Metz, C. Burschka, and K. Taume Organomet 28 2009 2311
30. N.M. West, P.S. White, J.L. Templeton, and J.F. Nixon Organomet 28 2009 1425
31. F. Basuli, P. Chattopadhyay, and C. Sinha Polyhedron 15 1996 2439
32. D. Banerjee, U.S. Ray, J.-C. Liou, C.-N. Lin, T.-H. Lu, and C. Sinha Inorg. Chim. Acta 358 2005 1019
33. J. Otsuki, K. Suwa, K. Narutaki, C. Sinha, I. Yoshikawa, and K. Araki J. Phys. Chem. A 109 2005 8064
34. J.C. Vincent, and H.W. Vincent Pros. Soc. Exp. Biol. Med. 55 1944 162
35. J.B. Ellen, M.F. Sydney, Baily and Scott's Diagnostic Microbiology, eighth ed., USA, Missouri, 1990, p. 453.
36. L. Mishra, and V.K. Singh Inidian J. Chem. Sect. A 32A 1997 446
37. W. Levinson, E. Jawetz, Med. Microbiol. Immunol., fourth ed., Stamford, 1996.
38. F.A. Cotton, and G. Wilkinson Advanced Inorganic Chemistry fifth ed. 1988 John Wiley New York
39. F. Basolo, R.G. Pearson, Mechanisms of Inorganic Reactions, John Wiley and Son, New York, 1967, ISBN: 047105545X.
40. A.I. Vogel, A Text Book of Practical Organic Chemistry, second ed., Longman, London, 1959.
41. P. Chattopadhyay, and C. Sinha Polyhedron 13 1994 2689
42. G.M. Sheldrick shelxs 97, Program for the Solution of Crystal Structure 1997 University of Gottingen Germany
43. C.K. Johnson, ortep, Report ORNL-5138, Oak Ridge National Laboratory, TN, 1976.
44. diamond, Visual Crystal Structure Information System, Version 2.1e, CRYSTAL IMPACT, Postfach 1251, D-53002 Bonn, Germany, 2002.
45. Texsan, Structure Analysis Software, Molecular Structure Corp., The Woodlands, TX, 1997.
46. L.J. Farrugia J. Appl. Crystallogr. 30 1997 565
47. A.L. Spek platon, Molecular Geometry Program 1999 University of Utrecht The Netherlands
48. C. Lee, W. Yang, and R.G. Parr Phys. Rev. B 37 1988 785
49. D. Andrae, U. Haeussermann, M. Dolg, H. Stoll, and H. Preuss Theor. Chim. Acta 77 1990 123
50. M.J. Frisch, G.M. Trucks, H.B. Schlegel, G.E. Scuseria, M.A. Robb, J.R. Cheeseman, J.A. Montgomery, T. Vreven Jr., K.N. Kudin, J.C. Burant, J.M. Millam, S.S. Iyengar, J. Tomasi, V. Barone, B. Mennucci, M. Cossi, G. Scalmani, N. Rega, G.A. Petersson, H. Nakatsuji, M. Hada, M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, Y. Honda, O. Kitao, H. Nakai, M. Klene, X. Li, J.E. Knox, H.P. Hratchian, J.B. Cross, V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R.E. Stratmann, O. Yazyev, A.J. Austin, R. Cammi, Pomelli, J.W. Ochterski, P.Y. Ayala, K. Morokuma, G.A. Voth, P. Salvador, J.J. Dannenberg, V.G. Zakrzewski, S. Dapprich, A.D. Daniels, M.C. Strain, O. Farkas, D.K. Malick, A.D. Rabuck, K. Raghavachari, J.B. Foresman, J.V. Ortiz, Q. Cui, A.G. Baboul, S. Clifford, J. Cioslowski, B.B. Stefanov, G. Liu, A. Liashenko, P. Piskorz, I. Komaromi, R.L. Martin, D.J. Fox, T. Keith, M.A. Al-Laham, C.Y. Peng, A. Nanayakkara, M.Challacombe, P.M.W. Gill, B. Johnson, W. Chen, M.W. Wong, C. Gonzalez, J.A. Pople, Gaussian, Inc., Wallingford CT, 2004.
51. gaussview3.0, Gaussian, Pittsburgh, PA.
52. R. Bauernschmitt, and R. Ahlrichs Chem. Phys. Lett. 256 1996 454
53. M. Cossi, N. Rega, G. Scalmani, and V. Barone Comput. Chem. 24 2003 669
54. N.M. O'Boyle, A.L. Tenderholt, and K.M. Langner J. Comp. Chem. 29 2008 839
55. National Committee for Clinical Laboratory Standards (NCCLS), thirdrd ed., Approved Standard M7-A3, NCCLS, Villanova, PA, 1993.
56. D. Chattopadhyay, S.G. Dastidar, and A.N. Chakrabarty Arzneim Forsch (II) 38 1988 869
57. D. Chattopadhyay, T. Mukherjee, P. Pal, B. Saha, and R. Bhadra J. Antimicrob. Chemother. 42 1998 83
58. P. Chattopadhyay, B. Sinha, and L.K. Vaid Fitoterapia 69 1998 365
59. D. Chattopadhyaya, and A.K. Maiti J. Ethnopharmacol. 77 2001 49
60. .
61. T.S. Roopashree, R. Dang, R.H. Shobha Rani, C. Narendra, Int. J. Appl. Res. Nat. Prod. 1 (2008) 20.