DOI QR코드

DOI QR Code

Synthesis and Characterization of New Group 13 Complexes of 2-Acetylpyridine-S-methyldithiocarbazate. Single-Crystal Structure of Me₂Ga[$NC_5H_4C$(CH₃)NNC(S)SMe] and Me₂In[$NC_5H_5C$(CH₃)NNC(S)SMe]

  • Published : 1997.03.20

Abstract

The synthesis and characterization of the mononuclear group 13 heterocyclic carboxaldehyde methyldithiocarbazate complexes Me2M[NC5H4CRNNC(S)SCH3] (M=Al, R=H(1); M=Ga, R=H(2); M=Al, R=CH3(3); M-Ga, R=CH3(4); M=In, R=CH3(5)) are described. Compounds 1-5 were prepared by the reaction of MMe3 (M=Al, Ga, In) with 2-formy or 2-acetylpyridine-S-methyldithiocarbazate in toluene. These compounds 1-5 have been characterized by microanalysis, NMR (1H, 13C) spectroscopy, mass spectra, and single-crystal X-ray diffraction. X-ray single-crystal diffraction analyses reveal that 4-5 are mononuclear metal compounds with coordination number of 5 and N,N,S coordination mode.

Keywords

References

  1. Bioinorg. Chem. v.3 Winkelmann, D. A.;Bermke, Y.;Petering, D. H.
  2. Mol. Pharmacol v.13 Antholine, W. E.;Knight, J. M.;Whelan, H.;Petering, D. H.
  3. Inorg. Chem. v.16 Antholine, W. E.;Knight, J. M.;Petering, D. H.
  4. Proc. Roy. Irish. Acad v.65B Barry, V. C.;Conalty, M. L.;O'Callaghan, C. N.;Towmey, D.
  5. J. Chem. Soc., Dalton Trons. Binfham, A. G.;Bogge, H.;Muller, A.;Ainscough, E. W.;Brodie, A. M.
  6. J. Chem. Soc., Dalton Trons. Ainscough, E. W.;Brodie, A. M.;Ranford, J. D.;Waters, J. M.
  7. J. Chem. Soc., Dalton Trons. Ainscough, E. W.;Brodie, A. M.;Ranford, J. D.;Wasters, J. M.
  8. Transition Met. Chem. v.15 West, E. X.;Carlson, C. S.;Galloway, C. P.;Liberta, A. E.;Daniel, C. R.
  9. Anti-Cancer Drugs v.4 West,. D. X.;Liberta, A. E.;Rajendran, K.;Hall, I. H.
  10. Inorg. Chim. Acta. v.172 Ainscough, E. W.;Baker, E. N.;Brodie, A. M.;Cresswell, R. J.;Ranford, J. D.
  11. Transition Met. Chem. v.15 West, D. X.;Carlson, C. S.;Liberta, A. E.;Scovill, J. P.
  12. Transition Met. Chem. v.15 West, D. X.;Carlson, C. S.;Liberta, A. E.;Albert, J. N.;Daniel, C. R.
  13. J. Am. Chem. Soc. v.91 Mathew, M.;Palenik, G. J.
  14. Transition Met. Chem. v.15 West, D. X.;Carlson, C. S.;Whyte, A. C.;Liberta, A. E.
  15. Synth. React. Inorg. Met-org. Chem. v.18 Grag, A.;Tandon, J. P.
  16. Inorg. Chim. Acta. v.67 Raina, R.;Srivastava, T. S.
  17. Inorg. Chim. Acta. v.75 Beraldo, H.;Tosi, L.
  18. J. Chem. Soc., Dalton Trons. Casas, . C.;Castano, M. V.;Rodriguez-Arguelles, M. C.;Sanchez, A.;Sordo, J.
  19. Int. J. Nucl. med. Biol. v.8 Moerlein, S. M.;Welch, M. J.
  20. J. Nucl. Med. v.10 Edwards, G. L.;Hayes, R. L.
  21. Inorg. Met.-Org. Chem. v.21 Kratz, F.;Nuber, B.;Weiβ, J.;Keppler, B. K.
  22. Accepted for publication to Organometallics Paek, C.;Kang, S. O.;Ko, J.;Barkely, J. V.
  23. Accepted for publication to Organometallics Paek, C.;Kang, S. O.;Ko, J.
  24. J. Med. Chem. v.25 Scovill, J. P.;Klayman, D. L.;Franchino, C. F.
  25. Organometallics v.14 Atwood, D. A.;Rutherford, D.
  26. Inorg. Chem. v.34 Rose, D. J.;Chang, Y. D.;Chen, Q.;Kettler, P. B.;Zubieta, J.
  27. Organometallics v.15 Trepanier, S.;Wang, S.
  28. Can. J. Chem. v.54 Rettig, s. T.;Storr, A.;Trotter, J.
  29. Can. J. Chem. v.53 Rettig, S. T.;Storr, A.;Trotter, J.
  30. Can. J. Chem. v.53 Rettig, S. T.;Storr, A.;Trotter, J.
  31. Organometallics v.9 Lee, B.;Pennington, W. T.;Robinsonm, G. H.
  32. Inorg. Chem. v.35 Zhou, Y.;Richeson, D. S.
  33. Organometallics v.9 Reger, D. L.;Knox, S. J.
  34. Inorg. Chem. v.19 Khan, M.;Steevensz, R. C.;Tuck, D. G.;Noltes, J. G.;Corfield, P. W. R.
  35. Organometallics v.9 Refer, D. L.;Knox, S. J.
  36. Organometallics v.12 Leman, J. T.;Roman, H. A.;Barron, A. R.
  37. J. Organomet. Chem. v.479 Schumann, H.;Seuβ, T. D.;Weimann, R.;Hemling, H.;Grorlitz, F. H.
  38. Organometallics v.14 Zhou, Y.;Richeson, D. S.