The reactions of heterocyclic organotellurium and selenium compounds with triiron dodecacarbonyl

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Zulfiqar Majeed, William R. McWhinnie, Keith Paxton and Thomas A. Hamor


Abstract

The reaction of 2-telluraphthalide, C8H6OTe, with [Fe3(CO)12] gave as the major characterised species compound 1, [[upper bond 1 start]C6H4CH2TeF[upper bond 1 end]e(CO)3]2. An iron atom has inserted into the telluracyclic ring, and it is probable that one co-ordinated CO ligand arises from the initially organic carbonyl group. X-Ray single crystal investigations revealed a dimeric structure containing an Fe2Te2 core. The reaction of 2-telluraphthalic anhydride, C8H4O2Te, with [Fe3(CO)12] gave a known, but unexpected, organic product phthalide, C8H6O2. X-Ray crystallography confirmed its isolation; the main feature of interest is the significant double bond character of C(8)–O(1) at 1.352(4) Å. 2-Selenaphthalic anhydride, C8H4O2Se, gave intractable products on reaction with [Fe3(CO)12], but 2-selenaphthalide, C8H6OSe, on reaction with the carbonyl gave a major product 2, [Fe(CO)3{[upper bond 1 start]C6H4CH2SeF[upper bond 1 end]e(CO)3}] and a minor product 3, [Fe(CO)26-C6H4CH2SeFe2(CO)6}] which is an intermediate in the formation of 2. Compound 2 was shown by X-ray methods to be very similar to 1 except that the 18 electron rule is satisfied by co-ordination of an Fe(CO)3 moiety, rather than by dimerisation. Compound 3, also studied by X-ray crystallography, differs from 2 mainly in the addition of an η6-bonded Fe(CO)2 moiety, but the selenaferrole ring is more distorted. It is proposed that comparative studies of reactions of selenium and tellurium compounds with [Fe3(CO)12] may assist the development of an understanding of the complex reaction pathways.


References

  1. K. Singh, W. R. McWhinnie, H. L. Chen, M. Sun and T. A. Hamor, J. Chem. Soc., Dalton Trans, 1996, 1545 RSC.
  2. K. Badyal, W. R. McWhinnie, H. L. Chen and T. A. Hamor, J. Chem. Soc., Dalton Trans., 1997, 1579 RSC.
  3. K. Badyal, W. R. McWhinnie, T. A. Hamor and H. Chen, Organometallics, 1997, 16, 3194 CrossRef CAS.
  4. T. B. Rauchfuss, Prog. Inorg. Chem., 1991, 39, 259.
  5. R. J. Angelici, Coord. Chem. Rev., 1990, 105, 61 CrossRef CAS.
  6. (a) M. G. Choi and R. J. Angelici, J Am. Chem. Soc., 1991, 113, 5651 CrossRef CAS; (b) C. J. White, T. L. Wang, R. A. Jacobsen and R. J. Angelici, Organometallics, 1994, 13, 4474 CrossRef CAS; (c) C. J. White and R. J. Angelici, Organometallics, 1994, 13, 5132 CrossRef CAS.
  7. K. Badyal, W. R. McWhinnie, J. Homer and M. C. Perry, J. Organomet. Chem., 1998, in the press Search PubMed.
  8. L. Engman and M. P. Cava, J. Org. Chem., 1981, 46, 4194 CrossRef CAS.
  9. (a) J. Bergman and L. Engman, Org. Prep. Proced. Int., 1978, 10, 289 CAS; (b) Z. Majeed, W. R. McWhinnie, K. Paxton and T. A. Hamer, J. Organomet. Chem., in the press Search PubMed.
  10. W. H. H. Gunther, J. Org. Chem., 1967, 32, 3929 CrossRef.
  11. TEXSAN, Single Crystal Structure Analysis Software, version 1.6, Molecular Structure Corporation, Houston, TX, 1993.
  12. G. M. Sheldrick, SHELXL 93, Program for Crystal Structure Refinement, University of Göttingen, 1993.
  13. C. K. Johnson, ORTEP, Report ORNL-5138, Oak Ridge National Laboratory, Oak Ridge, TN, 1976.
  14. A. Klose, E. Solari, C. Floriani, N. Re, A. Chiesivila and C. Rizzoli, Chem. Commun., 1997, 2297 RSC.
  15. P. Mathur, D. Chakrabarty, M. M. Hossain, R. S. Rashid, V. Rugmini and A. L. Rheingold, Inorg. Chem., 1992, 31, 1106 CrossRef CAS; G. Gervasio, J. Organomet. Chem., 1992, 441, 271 CrossRef CAS; L. C. Roof, D. M. Smith, G. W. Drake, W. T. Pennington and J. W. Kolis, Inorg. Chem., 1995, 34, 337 CrossRef CAS; J. R. Eveland and K. H. Whitmire, Angew. Chem., Int. Ed. Engl., 1996, 35, 741 CrossRef CAS.
  16. F. H. Allen, O. Kennard, D. G. Watson, L. Brammer, A. G. Orpen and R. Taylor, J. Chem. Soc., Perkin Trans., 1987, S1 Search PubMed.
  17. K. Y. Abid, N. I. Al-Salim, M. Greaves, W. R. McWhinnie, A. A. West and T. A. Hamor, J. Chem. Soc., Dalton Trans., 1989, 1697 RSC; H. B. Singh, N. Sudha, A. A. West and T. A. Hamor, J. Chem. Soc., Dalton Trans., 1990, 907 RSC.
  18. R. B. Bates and R. S. Cutler, Acta Crystallogr., Sect. B, 1977, 33, 893 CrossRef.
  19. R. C. Petterson, K. H. Pannell and A. J. Mayr, Acta Crystallogr., Sect. B, 1980, 36, 2434 CrossRef.
  20. N. S. Nametkin, V. D. Tyurin, A. I. Nekhaev, Yu. P. Sobolev, M. G. Kondrateva, A. S. Batsanov and Yu. T. Struchkov, J. Organomet. Chem., 1983, 243, 323 CrossRef CAS.
  21. J. Chen, J. Yin, Z. Fan and W. Xu, J. Chem. Soc., Dalton Trans., 1988, 2803 RSC.
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