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Synthesis and Crystal Structures of Mn(II), Co(II), Ni(II), Cu(II), and Zn(II) Metal Complexes with NNO Functionalized Ligands

  • Jang, Yoon-Jung (Department of Chemistry, Catholic University of Daegu) ;
  • Lee, Uk (Department of Chemistry, Pukyong National University) ;
  • Koo, Bon-Kweon (Department of Chemistry, Catholic University of Daegu)
  • Published : 2005.06.20

Abstract

Some new metal(II) complexes, $M^{II}L_2$ [M = Mn (1), Co (2), Ni (3), Cu (4), and Zn (5)] of 2-acetylpyridine benzoylhydrazone ligand (HL) containing trifunctional NNO-donor system have been synthesized and crystallographically characterized for the complex 1 and 5. The complexes consist of two ligands to give sixcoordinate, which are bonded to the metal atom on a meridional plane through acetylpyridine ring nitrogen, azomethine nitrogen, and benzoyl oxygen atoms, respectively. The coordination geometry for other complexes was identified on the basis of the physicochemical data by elemental analyses, FAB -MS, IR, $^1H$ NMR, and electronic spectral measurements. The resulting data indicated that the complexes are accordance with the above formulation.

Keywords

References

  1. McCleverty, J. A.; Meyer, T. J. Comprehensive Coordination Chemistry II; Molina, H. R.; Mederos, A., Eds.; Elsevier: London, The United Kingdom, 2004; Vol. 31
  2. Stelzig, L.; Kotte, S.; Krebs, B. J. Chem. Soc. Dalton Trans. 1998, 2921
  3. Rana, A.; Dinda, R.; Sengupta, P.; Ghosh, S.; Falvello, L. R. Polyhedron 2002, 21, 1023 https://doi.org/10.1016/S0277-5387(02)00913-0
  4. Bustos, C.; Burckhardt, O.; Schrebler, R.; Carrillo, D.; Arif, A. M.; Cowley, A. H.; Nunn, C. M. Inorg. Chem. 1990, 29, 3996 https://doi.org/10.1021/ic00345a017
  5. Rana, A.; Dinda, R.; Ghosh, S.; Blake, A. Polyhedron 2003, 22, 3075 https://doi.org/10.1016/j.poly.2003.06.001
  6. Costamagna, J.; Vargas, J.; Latorre, R.; Alvarado, A.; Mena, G. Coord. Chem. Rev. 1992, 119, 67 https://doi.org/10.1016/0010-8545(92)80030-U
  7. Tandon, S. S.; Chander, S.; Thompson, L. K. Inorg. Chim. Acta 2000, 300-302, 683 https://doi.org/10.1016/S0020-1693(00)00010-4
  8. Oshio, H.; Toriumi, M. Y.; Takashima, Y. Inorg. Chem. 1991, 30, 4252 https://doi.org/10.1021/ic00022a029
  9. Nazir, H.; Yildiz, M.; Yilmaz, H.; Tahir, M. N.; Ulku, D. J. Mol. Struct. 2000, 524, 241 https://doi.org/10.1016/S0022-2860(00)00393-8
  10. Jeffery, J. C.; Thornton, P.; Ward, M. D. Inorg. Chem. 1994, 33, 3612 https://doi.org/10.1021/ic00094a029
  11. Dutta, S. K.; Tiekink, E. R. T.; Chaudhury, M. Polyhedron 1997, 16, 1863 https://doi.org/10.1016/S0277-5387(96)00491-3
  12. Scovill, J. P. Phosphorus, Sulfur, and Silicon 1991, 60, 15 https://doi.org/10.1080/10426509108233920
  13. Pessoa, J. C.; Tomaz, I.; Henriques, R. T. Inorg. Chim. Acta 2003, 356, 121 https://doi.org/10.1016/S0020-1693(03)00395-5
  14. Ando, R.; Yagyu, T.; Maeda, M. Inorg. Chim. Acta 2004, 357, 2237 https://doi.org/10.1016/j.ica.2003.12.031
  15. Ando, R.; Mori, S.; Hayashi, M.; Yagyu, T.; Maeda, M. Inorg. Chim. Acta 2004, 357, 1177 https://doi.org/10.1016/j.ica.2003.09.033
  16. Mo, S. J.; Lim, W. T.; Koo, B. K. Bull. Korean Chem. Soc. 1998, 19, 1175
  17. Mo, S. J.; Koo, B. K. Bull. Korean Chem. Soc. 1999, 20, 1225
  18. Lee, U.; Koo, B. K. Bull. Korean Chem. Soc. 2002, 23, 613 https://doi.org/10.5012/bkcs.2002.23.4.613
  19. Koo, B. K.; Jang, Y. J.; Lee, U. Bull. Korean Chem. Soc. 2003, 24, 1014 https://doi.org/10.5012/bkcs.2003.24.7.1014
  20. Jang, Y. J.; Mo, S. J.; Koo, B. K. Bull. Korean Chem. Soc. 1998, 19, 1124
  21. Mo, S. J.; Koo, B. K. Bull. Korean Chem. Soc. 1999, 20, 1105
  22. Kim, D. W.; Lee, U. Bull. Korean Chem. Soc. 2004, 25, 1071 https://doi.org/10.5012/bkcs.2004.25.7.1071
  23. Pelagatti, P.; Carcelli, M.; Pelizzi, C.; Costa, M. Inorg. Chim. Acta 2003, 342, 323 https://doi.org/10.1016/S0020-1693(02)01161-1
  24. Naskar, S.; Biswas, S.; Mishra, D.; Adhikary, B.; Falvello, L. R.; Soler, T.; Schwalbe, C. H.; Chattopadhyay, S. K. Inorg. Chim. Acta 2004, 357, 4257 https://doi.org/10.1016/j.ica.2004.06.018
  25. Karunakar, G. V. et al. J. Coord. Chem. 2000, 50, 51 https://doi.org/10.1080/00958970008054924
  26. Amstrong, C. M. et al. Eur. J. Inorg. Chem. 2003, 1145
  27. Patole, J.; Sandbhor, U.; Padhye, S.; Deobagkar, D. N.; Anson, C. E.; Powell, A. Bioorg. Med. Chem. Lett. 2003, 13, 51 https://doi.org/10.1016/S0960-894X(02)00855-7
  28. STOE STAD14, X-RED & X-SHAPE, X-ray structure evaluation package; STOE-Cie GMbh: Hilpertstrase 10, D64295, Darmstadt, Germany, 1996
  29. Sheldrick, G. M. Acta Cryst. 1990, A46, 467
  30. Sheldrick, G. M. SHELXS97-2 and SHELXL97-2; University of Gottingen: Gottingen, Germany, 1997
  31. Geary, W. J. Coord. Chem. Rev. 1971, 7, 81 https://doi.org/10.1016/S0010-8545(00)80009-0
  32. Farrugia, L. J. J. Appl. Cryst. 1997, 30, 565
  33. Fegy, K.; Sanz, N.; Luneau, D.; Belorizky, E.; Rey, P. Inorg. Chem. 1998, 37, 4518 https://doi.org/10.1021/ic971618l
  34. Dutta, S.; Basy, P.; Chakravorty, A. Inorg. Chem. 1991, 30, 4031 https://doi.org/10.1021/ic00021a012
  35. Yamami, M.; Tanaka, M.; Sakiyama, H.; Koga, T.; Kobayashi, K.; Miyasaka, H.; Ohba, M.; Okawa, H. J. Chem. Soc. Dalton Trans. 1997, 4595
  36. Patra, A. K.; Mukherjee, R. Inorg. Chem. 1999, 38, 1388 https://doi.org/10.1021/ic980672e
  37. Ray, M. S.; Bhattacharya, R.; Chaudhuri, S.; Righi, L.; Bocelli, G.; Mukhopadhyay, G.; Ghosh, A. Polyhedron 2003, 22, 617 https://doi.org/10.1016/S0277-5387(02)01435-3
  38. Dey, M.; Rao, C. P.; Saarenketo, P. K.; Rissanen, K. Inorg. Chem. Commun. 2002, 5, 924 https://doi.org/10.1016/S1387-7003(02)00602-0
  39. Yang, C. T.; Vittal, J. J. Inorg. Chim. Acta 2003, 344, 65 https://doi.org/10.1016/S0020-1693(02)01269-0
  40. Dung, N. H.; Viossat, B.; Busnot, A.; Gonzalez Perez, J. M.; Gonzalez Garcia, S.; Gutierrez, J. N. Inorg. Chem. 1987, 26, 2365 https://doi.org/10.1021/ic00262a006
  41. Sorrell, T. N.; Allen, W. E.; White, P. S. Inorg. Chem. 1995, 34, 952 https://doi.org/10.1021/ic00108a030
  42. Asada, H.; Hayashi, K.; Negoro, S.; Fujiwara, M.; Matsushita, T. Inorg. Chem. Commun. 2003, 6, 193 https://doi.org/10.1016/S1387-7003(02)00718-9
  43. Saha, N.; Mukherjee, N. Polyhedron 1984, 3, 1135 https://doi.org/10.1016/S0277-5387(00)88070-5

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