A new route to mixed oxo/arylimido complexes of molybdenum(VI) with a tris(pyrazolyl)borate co-ligand: syntheses, spectroscopic properties and ligand-centred redox activity

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Siu-Ming Lee, Ralph Kowallick, Massimo Marcaccio, Jon A. McCleverty and Michael D. Ward


Abstract

Reaction of the oxo-molybdenum(V) precursor [Mo(TpMe,Me)(O)Cl2] [TpMe,Me [double bond, length half m-dash] hydrotris(3,5-dimethylpyrazol-1-yl)borate] with arylamines RNH2, in the presence of Et3N and air, afforded the oxo(imido)molybdenum(VI) complexes [Mo(O)(TpMe,Me)Cl([double bond, length half m-dash]NR)] 1 (R = 4-tolyl), 2 (R = C6H4NMe2-4); this is a new and simple route to these rare compounds. Use of 1,4-diaminobenzene afforded the mononuclear complex 3 (R = C6H4NH2-4) in addition to the dinuclear complex [{Cl(O)(TpMe,Me)Mo}2 (NC6H4N)] 4. Reaction of various aminoferrocene derivatives Fc–X–NH2 with [Mo(TpMe,Me)(O)Cl2] afforded the dinuclear ferrocenyl–molybdenum complexes [Mo(O)(TpMe,Me)Cl([double bond, length half m-dash]NXFc)] 5 (X = nothing), 6 (X = 1,4-C6H4), 7 (X = C6H4CH[double bond, length half m-dash]CHC6H4 with all para substitution) and 8 (X = C6H4N[double bond, length half m-dash]NC6H4 with all para substitution). Reaction of [Mo(TpMe,Me)(O)Cl2] with mixed amine–phenol ligands HO–X–NH2 afforded the mixed-valence complexes [{Cl(O)(TpMe,Me)Mo}2([double bond, length half m-dash]NXO)] 9 (X = 1,4-C6H4) and 10 (X = 1,5-naphthalenediyl), and the mononuclear oxo-Mo(V) complex [Mo(O)(TpMe,Me)Cl(OC6H4NH2)] 9a with an unreacted amino terminus was also isolated. The complexes were characterised by 1H NMR and IR spectroscopy, FAB mass spectrometry and UV/VIS spectroscopy. Whereas the simple oxo-imido-Mo(VI) cores of 1 and 5–10 undergo completely irreversible oxidations, complexes 2 and 3 undergo two reversible ligand-centred oxidations, one of the pendant amino group to give a radical cation, and the second of the imido fragment resulting in a quinonoidal structure {Mo[double bond, length half m-dash]N[double bond, length half m-dash]C6H4[double bond, length half m-dash]NR2}2+ (R = Me, H) for the arylimido ligand. Similarly in complex 4 the bridging fragment Mo[double bond, length half m-dash]NC6H4N[double bond, length half m-dash]Mo undergoes two reversible oxidations to give the quinonoidal dication {Mo[double bond, length half m-dash]N[double bond, length half m-dash]C6H4[double bond, length half m-dash]N[double bond, length half m-dash]Mo}2+via the semiquinone radical intermediate. Spectroelectrochemical studies on 2 and 4 confirmed the nature of these reversible oxidations as ligand centred. Complexes 5 to 8 undergo a reversible oxidation of the ferrocenyl fragment, and complexes 9, 9a and 10 display the reversible Mo(V)/Mo(VI) and Mo(V)/Mo(IV) redox couples expected for their oxo-Mo(V) fragments.


References

  1. D. E. Wigley, Prog. Inorg. Chem., 1994, 42, 239 CAS; W. A. Nugent and B. L. Haymore, Coord. Chem. Rev., 1980, 31, 123 CrossRef CAS.
  2. C. Y. Chou, J. C. Huffman and E. A. Maatta, J. Chem. Soc., Chem. Commun., 1984, 1184 RSC; B. L. Haymore, E. A. Maatta and R. A. D. Wentworth, J. Am. Chem. Soc., 1979, 101, 2063 CrossRef CAS; V. C. Gibson, E. L. Marshall, C. Redshaw, W. Clegg and M. R. J. Elsegood, J. Chem. Soc., Dalton Trans., 1996, 4197 RSC.
  3. E. W. Harlan and R. H. Holm, J. Am. Chem. Soc., 1990, 112, 186 CrossRef CAS.
  4. R. R. Schrock, Acc. Chem. Res., 1990, 23, 158 CrossRef CAS; R. R. Schrock, Pure Appl. Chem., 1994, 66, 1447 CAS; C. Pariya, K. N. Jayaprakash and A. Sarkar, Coord. Chem. Rev., 1998, 168, 1 CrossRef CAS.
  5. D. D. Devare and E. A. Maatta, Inorg. Chem., 1985, 24, 2846 CrossRef CAS; E. A. Maatta and R. A. D. Wentworth, Inorg. Chem., 1979, 18, 2409 CrossRef CAS.
  6. J. Takacs and R. G. Cavell, Inorg. Chem., 1994, 33, 2635 CrossRef CAS.
  7. G. R. Clark, A. J. Nielson and C. E. F. Rickard, J. Chem. Soc., Dalton Trans., 1996, 4265 RSC.
  8. W. M. Vaughan, K. A. Abboud and J. M. Boncella, J. Organomet. Chem., 1995, 485, 37 CrossRef CAS.
  9. J. Chatt, R. Choukroun, J. R. Dilworth, J. Hyde, P. Vella and J. Zubieta, Transition Met. Chem. (Weinheim, Ger.), 1979, 4, 59 Search PubMed.
  10. M. L. H. Green, G. Hogarth, P. C. Konidaris and P. Mountford, J. Chem. Soc., Dalton Trans., 1990, 3781 RSC.
  11. A. Wlodarczyk, G. A. Doyle, J. P. Maher, J. A. McCleverty and M. D. Ward, Chem. Commun., 1997, 769 RSC; J. Hock, A. M. W. Cargill Thompson, J. A. McCleverty and M. D. Ward, J. Chem. Soc., Dalton Trans., 1996, 4257 RSC; A. M. W. Cargill Thompson, D. Gatteschi, J. A. McCleverty, J. A. Navas Badiola, E. Rentschler and M. D. Ward, Inorg. Chem., 1996, 35, 2701 CrossRef.
  12. V. A. Ung, A. M. W. Cargill Thompson, D. A. Bardwell, D. Gatteschi, J. C. Jeffery, J. A. McCleverty, F. Totti and M. D. Ward, Inorg. Chem., 1997, 36, 3447 CrossRef; V. A. Ung, D. A. Bardwell, J. C. Jeffery, J. P. Maher, J. A. McCleverty, M. D. Ward and A. Williamson, Inorg. Chem., 1996, 35, 5290 CrossRef.
  13. B. J. Coe, T. A. Hamor, C. J. Jones, J. A. McCleverty, D. Bloor, G. Cross and T. L. Axon, J. Chem. Soc., Dalton Trans., 1995, 673 RSC; B. J. Coe, J.-D. Foulon, T. A. Hamor, C. J. Jones, J. A. McCleverty, D. Bloor, G. H. Cross and T. L. Axon, J. Chem. Soc., Dalton Trans., 1994, 3427 RSC.
  14. B. J. Coe, C. J. Jones, J. A. McCleverty, D. Bloor and G. Cross, J. Organomet. Chem., 1994, 464, 225 CrossRef CAS.
  15. S.-M. Lee, M. Marcaccio, J. A. McCleverty and M. D. Ward, Chem. Mater., in the press Search PubMed.
  16. W. E. Cleland, Jr., K. M. Barhhart, K. Yamanouchi, D. Collison, F. E. Mabbs, R. B. Ortega and J. H. Enemark, Inorg. Chem., 1987, 26, 1017 CrossRef.
  17. S. A. MacGregor, E. McInnes, R. J. Sorbie and L. J. Yellowlees, in Molecular Electrochemistry of Inorganic, Bioinorganic and Organometallic Compounds, eds. A. J. L. Pombiero and J. A. McCleverty, NATO ASI Series C, Kluwer Academic Publishers, 1993, vol. 385, pp. 503–517 Search PubMed.
  18. S. M. Charsley, C. J. Jones, J. A. McCleverty, B. D. Neaves, S. J. Reynolds and G. Denti, J. Chem. Soc., Dalton Trans., 1988, 293 RSC; S. M. Charsley, C. J. Jones and J. A. McCleverty, Transition Met. Chem., 1986, 11, 329 CrossRef CAS; N. J. Al-Obaidi, S. L. W. McWhinnie, T. A. Hamor, C. J. Jones and J. A. McCleverty, J. Chem. Soc., Dalton Trans., 1992, 3299 RSC.
  19. B. L. Westcott and J. H. Enemark, Inorg. Chem., 1997, 36, 5404 CrossRef CAS.
  20. K. Dehnicke and J. Strähle, Angew. Chem., Int. Ed. Engl., 1981, 20, 413 CrossRef.
  21. M. Minelli, M. R. Carson, D. W. Whisenhunt, Jr., W. Imhof and G. Huttner, Inorg. Chem., 1990, 29, 4801 CrossRef CAS.
  22. S. Granick and L. Michaelis, J. Am. Chem. Soc., 1940, 62, 2241 CrossRef CAS; G. Cauquis and D. Serve, Anal. Chem., 1972, 44, 2222 CrossRef CAS.
  23. M. D. Ward, Chem. Soc. Rev., 1995, 24, 121 RSC.
  24. W. Levason, R. Narayanaswamy, J. S. Ogden, A. J. Rest and J. W. Turff, J. Chem. Soc., Dalton Trans., 1982, 2009 RSC.
  25. M. M. Bhadbhade, A. Das, J. C. Jeffery, J. A. McCleverty, J. A. Navas Badiola and M. D. Ward, J. Chem. Soc., Dalton Trans., 1995, 2769 RSC; S. Toma, A. Gáplovský and I. Pavlík, Monatsh. Chem., 1985, 116, 479 CAS; S. Toma, A. Gáplovský, M. Hudecek and Z. Langfelderová, Monatsh. Chem., 1985, 116, 357 CAS.
  26. Y. S. Sohn, D. N. Hendrickson and H. B. Gray, J. Am. Chem. Soc., 1970, 92, 3233 CrossRef CAS; M. D. Rowe and A. J. McCaffery, J. Chem. Phys., 1973, 59, 3768; M. J. Carney, J. S. Lesniak, M. D. Likar and J. R. Pladziewicz, J. Am. Chem. Soc., 1984, 106, 2565 CrossRef CAS.
  27. A. Tsuchida, W. Sakai, M. Nakano and M. Yamamoto, J. Phys. Chem., 1992, 96, 8855 CrossRef CAS; H. D. Burrows, D. Greatrex and T. J. Kemp, J. Phys. Chem., 1972, 76, 20 CrossRef CAS.
  28. U. Nickel, E. Haase and W. Jaenicke, Ber. Bunsen-Ges. Phys. Chem., 1977, 81, 849 Search PubMed.
  29. T. Uémura and M. Abé, Bull. Chem. Soc. Jpn., 1937, 12, 59 CAS; J. F. Corbett, J. Chem. Soc. B, 1970, 1418 RSC; H. Shizuka, Y. Sawaguri and T. Morita, Bull. Chem. Soc. Jpn., 1972, 45, 24 CAS; H. Linschitz, M. Ottolenghi and R. Bensasson, J. Am. Chem. Soc., 1967, 89, 4592 CrossRef CAS.
  30. T. Sakata, M. Hiromoto, T. Yamagoshi and H. Tsubomura, Bull. Chem. Soc. Jpn., 1997, 50, 43.
  31. C. G. Pierpont and C. W. Lange, Prog. Inorg. Chem., 1993, 41, 381.
  32. L. F. Joulié, E. Schatz, M. D. Ward, F. Wever and L. J. Yellowlees, J. Chem. Soc., Dalton Trans., 1994, 799 RSC; A. M. Barthram, R. L. Cleary, J. C. Jeffery, S. M. Couchman and M. D. Ward, Inorg. Chim. Acta, 1998, 267, 1 CrossRef CAS; F. Hartl, T. J. Snoeck, D. J. Stufkens and A. B. P. Lever, Inorg. Chem., 1995, 34, 3887 CrossRef CAS.
  33. M. Emmelius, G. Pawlowski and H. W. Vollmann, Angew. Chem., Int. Ed. Engl., 1989, 28, 1445 CrossRef.
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