DOI QR코드

DOI QR Code

Synthesis and Crystal Structure of Manganese(II) Complexes with 2-Acetylpyridine Methyldithiocarbazate

  • Published : 1998.11.20

Abstract

The aerobic reaction of 2-(acetylpyridine)-S-methyldithiocarbazate (acpy-mdtcH) and 2-(acetylpyridine)-N-phenylthiosemicarbazate(acpy-phTscH) with manganese(Ⅱ) acetate affords Mn(acpy-mdtc)2 and Mn(acpyphTsc)2, respectively. The spectroscopic data and X-ray structure of Mn(acpy-mdtc)2 are reported. Crystal data for Mn(acpy-mdtc)2; C18H20N6S4Mn, mol wt 503.58, monoclinic crystal system(P21/c) a=12.240(5) Å, b= 10.918(l) Å, c=17.651(3) Å, β=105.93(2), and V=2268(l) Å3, Z=4, 5071 data collected with 0°< 2θ < 52.64°, 2995 data with I > 3σ(I), R= 0.046, Rw= 0.065. The ligands act as tridentate NNS donors. The two Mn-S distances are not equal, and respectively 2.512(2) Å and 2.541(2) Å. The average Mn-N (azomethine) length, 2.242(5) Å, is slightly shorter than the average Mn-N (pyridyl) length, 2.262(5) Å. The coordination environment about MN(Ⅱ) center deviates considerably from octahedral geometry. The manganese(Ⅱ)-manganese(Ⅰ) and manganese(Ⅰ)-manganese(0) reduction potentials of Mn(acpy-mdtc)2 are ∼-l.71 and ∼-l.98 V while those of Mn(acpy-phTsc)2 are ∼-l.87 and ∼-2.11 V vs. Ag/Ag+ in dimethyl sulfoxide, respectively.

Keywords

References

  1. Mangaese in Metabolism and Enzyme Function Beyer, W. F. Jr;Fridovich, I.
  2. Phtotochem. Photobiol. v.48 Pecoraro, V. L.
  3. Acc. Chem. Res. v.22 Christou, G.
  4. Prog. Inorg. Chem. v.37 Brudvig, G. W.;Crabtree, R. H.
  5. Adv. Inorg. Chem. v.33 Vincent, J. B.;Christou, G.
  6. Angew. Chem., Int. Ed. Engl. v.28 Wieghardt, K.
  7. Prog. Inorg. Chem. v.38 Que, L. Jr;True, A. E.
  8. J. Med. Chem. v.22 Klayman, D. L.;Bartosevich, J. F.;Griffin, T. S.;Mason, C. J.;Scovill, J. P.
  9. J. Med. Chem. v.22 Klayman, D. L.;Scovill, J. P.;Bartosevich, J. F.;Mason, C. J.
  10. J. Med. Chem. v.25 Scovill, J. P.;Klayman, D. L.;Franchino, C. F.
  11. J. Am. Chem. Soc. v.91 Mathew, M.;Palenik, G. J.
  12. J. Med. Chem. v.22 Saryan, L. A.;Ankel, E.;Krishnamurti, C.;Petering, D. H.;Elford, H.
  13. Inorg. Chim. Acta v.19 Das, M.;Livingstone, S. E.
  14. MULTAN 80 Main, P.;Fiske, S. J.;Hull, S. E.;Lessinger, L.;Germain, G.;Declerg, J. P.;Woolfson, M. M.
  15. Interactive Structure Solution Procedure MolEN
  16. Coord. Chem. Rev. v.7 Geary, W. J.
  17. Inorg. Chem. v.33 Jeffery, J. C.;Thornton, P.;Ward, M. D.
  18. Inorg. Chem. v.28 Bonadies, J. A.;Kirk, M. L.;Lah, M. S.;Kessissoglou, D. P.;Hatfield, W. E.;Pecoraro, V. L.
  19. Inorg. Chem. v.30 Dutta, S.;Basu, P.;Chakravorty, A.