FeIIPbII and FeIII complexes of macrocyclic compartmental ligands: different cyclization in stepwise template synthesis using FeII/PbII or FeIII/PbII pairs

(Note: The full text of this document is currently only available in the PDF Version )

Hideki Furutachi, Akiko Ishida, Hitoshi Miyasaka, Nobuo Fukita, Masaaki Ohba, Hisashi Ōkawa and Masayuki Koikawa


Abstract

The reaction of [bis(3-formyl-5-methylsalicylidene)ethylenediaminato]iron(II) with diethylenetriamine (dien) in the presence of PbII followed by the addition of NaNCS formed a FeIIPbII complex, [FePb(L1)(NCS)(dmf)(ClO4)] 1, where (L1)2– is a dinucleating macrocyclic compartmental ligand derived from the [2∶1∶1] condensation of 2,6-diformyl-4-methylphenol, ethylenediamine and dien, having “salen”- and “saldien”-like metal-binding sites sharing the phenolic entities. The Fe resides in the “salen” site and the Pb in the “saldien” site: the Fe[hair space][hair space]· · ·[hair space][hair space]Pb intermetallic separation is 3.438(2) Å. The Fe assumes a square-pyramidal geometry with an isothiocyanate nitrogen at the apex. The Pb has a seven-coordinate geometry with a dmf oxygen and a perchlorate oxygen at the axial sites. Complex 1 reacts with molecular dioxygen to give a µ-oxo complex [{FePb(L1)(NCS)(dmf)(ClO4)}2(O)]. A similar reaction of chloro[bis(3-formyl-5-methylsalicylidene)ethylenediaminato]iron(III) with dien in the presence of PbII formed a mononuclear FeIII complex [Fe(H2L2)(NCS)][ClO4]2·dmf 2, where H2L2 is a macrocycle derived from the [2∶2] condensation of 2,6-diformyl-4-methylphenol and dien. The Fe resides in one “saldien” site and assumes an octahedral geometry with an isothiocyanate nitrogen in one apical position. Another metal-binding site formed with dien shows unusual condensation; one primary amino group of the dien condenses with one formyl group to form an usual C[double bond, length half m-dash]N linkage and the remaining primary and secondary amino groups of the dien condense with another formyl group to form a five-membered imidazoline ring.


References

  1. D. E. Fenton and H. Ōkawa, Perspectives on Bioinorganic Chemistry, JAI Press, London, 1993, vol. 2, p. 81 Search PubMed; K. D. Karlin, Science, 1993, 261, 701 Search PubMed; Special thematic issue on “Metal-Dioxygen Complexes”, Chem. Rev., 1994, 94, 567–856 CAS; Special thematic issue on “Bioiorganic Enzymology”, Chem. Rev., 1996, 96, 2237–3042 CAS.
  2. N. Strater, T. Klabunde, P. Tucker, H. Witzel and B. Krebs, Science, 1995, 268, 1489 CAS.
  3. C. R. Kissinger, H. E. Parge, D. R. Knighton, C. T. Lewis, L. A. Pelletier, A. Tempczyk, V. J. Kalish, K. D. Tucker, R. E. Showalter, E. W. Moomaw, L. N. Gastinel, N. Habuka, X. Chen, F. Maldonado, J. E. Barker, R. Bacquet and J. E. Villafranca, Nature (London), 1995, 378, 641 CrossRef CAS.
  4. M.-P. Egloff, P. T. W. Cohen, P. Reinemer and D. Barford, J. Mol. Biol., 1995, 254, 942 CrossRef CAS.
  5. T. Tsukihara, H. Aoyama, E. Yamashita, T. Tomizaki, H. Yamaguchi, K. Shinzawa-Itoh, R. Nakashima, R. Yaono and S. Yoshikawa, Science, 1995, 269, 1069; 1996, 272, 1136 Search PubMed; S. Iwata, C. Ostermeier, B. Ludwig and H. Michel, Nature (London), 1995, 376, 660 Search PubMed.
  6. H. Ōkawa, H. Furutachi and D. E. Fenton, Coord. Chem. Rev., 1998, 174, 51 CrossRef CAS and refs. therein.
  7. H. Ōkawa, J. Nishio, M. Ohba, M. Tadokoro, N. Matsumoto, M. Koikawa, S. Kida and D. E. Fenton, Inorg. Chem., 1993, 32, 2949 CrossRef CAS.
  8. J. Nishio, H. Ōkawa, S. Ohtsuka and M. Tomono, Inorg. Chim. Acta, 1994, 218, 27 CrossRef CAS.
  9. J. Shimoda, H. Furutachi, M. Yonemura, M. Ohba, N. Matsumoto and H. Ōkawa, Chem. Lett., 1996, 979 CAS.
  10. H. Furutachi and H. Ōkawa, Inorg. Chem., 1997, 36, 3911 CrossRef CAS.
  11. H. Furutachi and H. Ōkawa, Bull. Chem. Soc. Jpn., 1998, 71, 671 CAS.
  12. M. Yamami, H. Furutachi, T. Yokoyama and H. Ōkawa, Chem. Lett., 1998, 211 CrossRef CAS.
  13. H. Furutachi, S. Fujinami, M. Suzuki and H. Ōkawa, Chem. Lett., 1998, 779 CrossRef CAS.
  14. N. F. Curtis, J. Chem. Soc., 1961, 3147 Search PubMed.
  15. E. A. Boudreaux and L. N. Mulay, Theory and Applications of Molecular Paramagnetism, Wiley, New York, 1976, pp. 491–494 Search PubMed.
  16. D. A. Denton and H. Suschitzky, J. Chem. Soc., 1963, 4741 RSC.
  17. H. Ōkawa and S. Kida, Inorg. Nucl. Chem. Lett., 1971, 7, 751 Search PubMed; H. Ōkawa and S. Kida, Bull. Chem. Soc. Jpn., 1972, 45, 1759 CAS; Y. Nishida, S. Oshio and S. Kida, Bull. Chem. Soc. Jpn., 1977, 50, 119 CAS.
  18. D. T. Cromer and J. T. Waber, International Tables for X-Ray Crystallography, Kynoch Press, Birmingham, vol. TV, 1974 Search PubMed.
  19. J. A. Ibers and W. C. Hamilton, Acta Crystallogr., 1964, 17, 781 CrossRef.
  20. D. C. Creagh and W. J. McAuley, International Tables for X-Ray Crystallography, ed. A. J. C. Wilson, Kluwer Academic Publishers, Boston, 1992, pp. 219–222 Search PubMed.
  21. D. C. Creagh and J. H. Hubbell, International Tables for X-Ray Crystallography, ed. A. J. C. Wilson, Kluwer Academic Publishers, Boston, 1992, pp. 200–206 Search PubMed.
  22. TEXSAN, Molecular Structure Corporation, Houston, TX, 1985.
  23. C. L. Spiro, S. L. Lambert, T. J. Smith, E. N. Duesler, R. R. Gagne and D. N. Hendrickson, Inorg. Chem., 1981, 20, 1229 CrossRef CAS.
  24. H. Furutachi and H. Ōkawa, unpublished work..
  25. M. Yamami, H. Furutachi, T. Yokoyama and H. Ōkawa, Inorg. Chem., in the press Search PubMed.
  26. K. Nakamoto, Infrared and Raman Spectra of Inorganic and Coordination Compounds, John Wiley & Sons, New York, 3rd edn., 1978, p. 270 Search PubMed.
  27. (a) A. Earnshaw, E. A. King and L. F. Larkworthy, J. Chem. Soc. A, 1968, 1048 RSC; (b) F. Calderazzo, C. Floriani, R. Henzi and F. L'Eplattenier, J. Chem. Soc. A, 1969, 1378 RSC.
  28. W. J. Geary, Coord. Chem. Rev., 1971, 7, 81 CrossRef CAS.
  29. B. Bosnich, J. Am. Chem. Soc., 1968, 90, 627 CrossRef CAS.
  30. J. Sanders, W. D. Wheeler, A. K. Shiemke, B. A. Averill and T. M. Loehr, J. Am. Chem. Soc., 1989, 111, 8084 CrossRef CAS.
  31. D. M. Kurtz, jun., Chem. Rev., 1990, 90, 585 CrossRef CAS; L. Que, jun. and A. E. True, Prog. Inorg. Chem., 1990, 38, 97; R. C. Reem, J. M. McCormick, D. E. Richardson, F. J. Devlin, P. J. Stephens, R. L. Musselman and E. I. Solomon, J. Am. Chem. Soc., 1989, 111, 4688 CrossRef CAS.
  32. C. K. Johnson, ORTEP, Report 3794, Oak Ridge National Laboratory, Oak Ridge, TN, 1965.
  33. S. Tamburini, P. A. Vigato, D. Chiarello and P. Traldi, Inorg. Chim. Acta, 1989, 156, 271 CrossRef CAS; M. G. B. Drew, J. Nelson and S. Nelson, J. Chem. Soc., Dalton Trans., 1981, 1678 RSC; R. Menif and A. E. Martell, J. Chem. Soc., Chem. Commun., 1989, 1521 RSC; R. Menif, A. E. Martell, P. J. Squattrito and A. Clearfield, Inorg. Chem., 1990, 29, 4723 CrossRef CAS; M. P. Ngwenya, D. Chen, A. E. Martell and J. Reibenspies, Inorg. Chem., 1991, 30, 2732 CrossRef CAS; K. Motoda, H. Sakiyama, N. Matsumoto, H. Ōkawa and S. Kida, Bull. Chem. Soc. Jpn., 1992, 65, 1176 CAS.
  34. H. Adams, N. A. Bailey, D. E. Fenton, R. J. Good, R. Moody and C. O. R. de Barbarin, J. Chem. Soc., Dalton Trans., 1987, 207 RSC; D. E. Fenton, S. J. Kitchen, C. M. Spencer, S. Tamburini and Vigato, J. Chem. Soc., Dalton Trans., 1988, 685 RSC.
  35. K. K. Nanda, S. K. Dutta, S. Baitalik, K. Venkatsubramanian and K. Nag, J. Chem. Soc., Dalton Trans., 1995, 1239 RSC; S. K. Dutta, R. Werner, U. Florke, S. Mohanta, K. K. Nanda, W. Haase and K. Nag, Inorg. Chem., 1996, 35, 2292 CrossRef CAS.