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Synthesis and Characterization of the Mixed-valence $[Fe^{II}Fe^{III}BPLNP(OAc)_2](BPh_4)_2$ Complex As a Model for the Reduced Form of the Purple Acid Phosphatase


Abstract

[Fe II Fe III $BPLNP(OAc)_2](BPh_4)_2$ (1), a new model for the reduced form of the purple acid phosphatases, has been synthesized by using a dinucleating ligand, 2,6-bis[((2-pyridylmethyl)(6-methyl-2-pyridylmethyl)ami-no)methyl]-4-nitrophenol (HBPLNP) . Complex 1 has been studied by electronic spectral, NMR, EPR, SQUID, and electrochemical methods. Complex 1 exhibits two strong bands at 498 nm $(\varepsilon=$ 2.6 ${\times}10^3M-^1cm-^1)$ and 1363 nm $(\varepsilon=$ 5.7 ${\times}10^2M-^1cm-^1)$ in $CH_3CN.$ These are assigned to phenolate-to-FeIII and intervalence charge-transfer transitions, respectively. NMR spectrum of complex 1 exhibits sharp isotropically shifted resonances, which number is half of those expected for a valence-trapped species, indicating that electron transfer between FeⅡ and FeⅢ centers is faster than NMR time scale at room temperature. Complex 1 undergoes quasireversible one-electron redox processes. The $FeIII_2/FeIIFeIII$ and $FeIIFeIII/FeII_2$ redox couples are at 0.807 and 0.167 V ver-sus SCE, respectively. It has Kcomp = 5.9 ${\times}$10 1s(acetato) ligand combination sta-bilizes a mixed-valence FeIIFeIII complex in the air. Interestingly, complex 1 exhibits intense EPR signals at g = 8.56, 5.45, 4.30 corresponding to mononuclear high-spin FeⅢ species, which suggest a very weak magnetic coupling between the iron centers. Magnetic susceptibility study shows that there is a very weak antiferromag-netic coupling (J = $-0.78cm-^1$, H = $-2JS_1${\times}$S_2)$ between FeII and FeIII centers. Thus, we can suggest that complex 1 has a very weak antiferromagnetic coupling between the iron centers due to the electronic effect of the nitro group in the bridging phenolate ligand.

Keywords

References

  1. Iron Carriers and Iron Proteins v.5 For recent reviews of these enzymes Sanders-Loehr, J.;Loehr, T. M.(ed.)
  2. Prog. Inorg. Chem. v.38 For recent reviews of these enzymes Que, L., Jr.;True, A. E.
  3. Chem. Rev. v.90 Vincent, J. B.;Oliver-Lilley, G. L.;Averill, B. A.
  4. Advances in Inorganic Chemistry v.43 Anderson, K. K.;Gruslund, A.
  5. Chem. Rev. v.96 Wilcox, D. E.
  6. Angew. Chem. Int. Ed. Engl. v.35 Strater, N.;Lipscomb, W. N.;Klabunde, T.;Krebs, B.
  7. Structure and Bonding v.89 Klabunde, T.;Krebs, B.
  8. Biochemistry v.20 Davis, J. C.;Lin, S. S.;Averill, B. A.
  9. J. Biol. Chem. v.257 Antanaitis, B. C.;Aisen, P.
  10. Adv. Inorg. Biochem. v.5 Antanaitis, B. C.;Aisen, P.
  11. J. Biol. Chem. v.257 Antanaitis, B. C.;Strekas, T.;Aisen, P.
  12. J. Am. Chem. Soc. v.109 Averill, B. A.;Davis, J. C.;Burman, S.;Zirino, T.;Sanders-Loehr, J.;Loehr, T. M.;Sage, J. T.;Debrunner, P. G.
  13. Eur. J. Biochem. v.199 Dietrich, M.;Munsternmann, D.;Suerbaum, H.;Witzel, H.
  14. Inorg. Chem. v.25 Kauzlarich, S. M.;Teo, B. K.;Zirino, T.;Burman, S.;Davis, J. C.;Averill, B. A.
  15. Biochemistry v.31 Crowder, M. W.;Vincent, J. B.;Averill, B. A.
  16. J. Biol. Chem. v.259 Antanaitis, B. C.;Aisen, P.
  17. Inorg. Chem. v.35 Lim, J. S.;Manuel, A. S.;Sykes, A. G.
  18. J. Biol. Chem. v.258 Antanaitis, B. C.;Aisen, P.;Lilienthal, H. R.
  19. J. Am. Chem. Soc. v.112 Davis, S. S.;Que, L., Jr.
  20. J. Biol. Chem. v.261 Pyrz, J. W.;Sage, J. T.;Debrunner, P. G.;Que, L., Jr.
  21. J. Biol. Chem. v.263 Day, E. P.;David, S. S.;Peterson, J.;Dunham, W. R.;Bonvoison, J. J.;Sands, R. H.;Que, L., Jr.
  22. J. Am. Chem. Soc. v.115 True, A. E.;Scarrow, R. C.;Randall, C. R.;Holz, R. C.;Que, L., Jr.
  23. J. Biol. Chem. v.258 Lauffer, R. B.;Antanaitis, B. C.;Aisen, P.;Que, L., Jr.
  24. J. Am. Chem. Soc. v.112 Scarrow, R. C.;Pyrz, J. W.;Que, L., Jr.
  25. Biochemistry v.31 Wang, Z.;Ming, L. J.;Que, L., Jr.
  26. Biochemistry v.31 Crans, D. C.;Simone, C. M.;Holz, R. C.;Que, L., Jr.
  27. Science v.268 Strater, N.;Klabunde, T.;Tucker, P.;Witzel, H.;Krebs, B.
  28. J. Mol. Biol. v.259 Klabunde, T.;Strater, N.;Frohlich, R.;Witzel, H.;Krebs, B.
  29. Nature v.345 Nordlund, P.;Sjoberg, B. M.;Eklund, H.
  30. Chem. Rev. v.96 Wallar, B. J.;Lipscomb, J. D.
  31. Bull. Chem. Soc. Jpn. v.60 Suzuki, M.;Uehara, A.;Oshio, H.;Endo, K.;Yanaga, M.;Kida, S.;Saito, K.
  32. J. Am. Chem. Soc. v.110 Borovik, A. S.;Que, L., Jr.
  33. J. Am. Chem. Soc. v.111 Borovik, S.;Papaefthymiou, V.;Taylor, L. F.;Anderson, O. P.;Que, L., Jr.
  34. Bull. Korean Chem. Soc. v.19 Yim, S. H.;Lee, H. J.;Lee, K.;Kang, S. J.;Hur, N. H.;Jang, H. G.
  35. J. Am. Chem. Soc. v.114 Mashuta, M. S.;Webb, R. J.;McCusker, J. K.;Schmitt, E. A.;Oberhausen, K. J.;Richardson, J. F.;Buchanan, R. M.;Hendrickson, D. N.
  36. J. Am. Chem. Soc. v.111 Mashuta, M. S.;Webb, R. J.;Oberhausen, K. J.;Richardson, J. F.;Buchanan, R. M.;Hendrickson, D. N.
  37. Bull. Chem. Soc. Jpn. v.61 Suzuki, M.;Oshio, H.;Uehara, A.;Endo, K.;Yanaga, M.;Kida, S.;Saito, K.
  38. J. Am. Chem. Soc. v.109 Borovik, A. S.;Murch, B. P.;Que, L., Jr.;Papaefthymiou, V.;Munck, E.
  39. Inorg. Chim. Acta. v.197 Neves, A.;Erthal, S. M. D.;Drago, V.;Griesar, K.;Haase, W.
  40. Inorg. Chem. v.35 Neves, A.;de Brito, M. A.;Vencato, I.;Drago, V.;Griesar, K.;Haase, W.;Mascarenhas, Y. P.
  41. Inorg. Chim. Acta v.214 Neves, A.;de Brito, M. A.;Vencato, I.;Drago, V.;Griesar, K.;Hasse, W.
  42. Inorg. Chim. Acta v.237 Neves, A.;de Brito, M. A.;Drago, V.;Griesar, K.;Haase, W.
  43. Inorg. Chem. v.33 Krebs, B.;Schepers, K.;Bremer, B.;Henkel, G.;Althaus, E.;Muller-Warmuth, W.;Griesar, K.;Haase, W.
  44. Inorg. Chem. v.34 Nie, H.;Aubin, S. M. J.;Mashuta, M. S.;Wu, C. C.;Richardson, J. F.;Hendrickson, D. N.;Buchanan, R. M.
  45. Inorg. Chem. v.31 Ming, L. J.;Jang, H. G.;Que, L., Jr.
  46. NMR of Paramagnetic Molecules in Biological Systems Bertini, I.;Luchinat, C.
  47. Adv. Inorg. Chem. and Radiochem. v.10 Robin, M. B.;Day, P.
  48. Prog. Inorg. Chem. v.30 Creutz, C.
  49. J. Am. Chem. Soc. v.103 Gagne, R. R.;Spiro, C. L.;Smith, T. J.;Hamann, C. A.;Thies, W. R.;Shuemke, A. K.
  50. Electron Spin Resonance: Elementary Theory and Practical Applications Wertz, J. E.;Bolton, J. R.
  51. Biochemistry v.11 Munck, E.;Debrunner, P. G.;Tsibris, J. C. M.;Gunsalus, I. C.
  52. Biophys. J. v.52 Day, E. P.;Kent, T. A.;Lindahl, P. A.;$M\"{u}nck$, E.;Orme-Johnson, W. H.;Roder, H.;Roy, A.

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