Selenium and tellurium derivatives of a monocarbon platinacarbaborane complex[hair space]

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

Stewart A. Batten, John C. Jeffery, Leigh H. Rees, Martin D. Rudd and F. Gordon A. Stone


Abstract

The reaction between Na[Pt(PEt3)25-7-CB10H11)] 1 and PhSeCl in thf (tetrahydrofuran) afforded a mixture containing the isomeric species [Pt(SePh)(PEt3)(η5-n-SePh-7-CB10H10)] (n = 8 2a or 9 2b) and the compound [Pt(SePh)(PEt3){η5-8-O(CH2)4Cl-7-CB10H10}] 3. The molecular structures of complexes 2a and 3 were established by X-ray crystallography. Both molecules have Pt(SePh)(PEt3) groups with the platinum atoms pentahapto co-ordinated by nido-7-CB10 cage frameworks. In 2a the cage substituted SePh group is attached to the boron atom in the α site with respect to the carbon in the [upper bond 1 start]CB[hair space]BBB[upper bond 1 end] ring ligating the platinum and this is true also of the O(CH2)4Cl substituent in 3. The isomers 2 are also formed when PhSeSePh is used instead of PhSeCl. Treatment of the salt 1 with PhTeI in thf yielded a mixture of [Pt(PEt3)25-9-Te(Ph)CH2Cl-7-CB10H10}] 4 and [Pt2(TePh)(µ-TePh)2(PEt3)25-2-CB10H11)] 5. Single-crystal X-ray diffraction studies were employed to establish the formulations and molecular structures of both molecules. Compound 4 is a charge-compensated platinacarbaborane with a Pt(PEt3)2 group and with the nido-7-CB10 framework carrying a Te(Ph)CH2Cl moiety at the boron vertex situated in the β site with respect to the carbon in the [upper bond 1 start]CBB[hair space]BB[upper bond 1 end] ring ligating the platinum. Complex 5 is a diplatinum species in which Pt(TePh)(PEt3) and Pt(PEt3)(η5-2-CB10H11) units are bridged by two TePh groups. The X-ray study revealed that in forming compound 5 from the reagent 1 the nido-7-CB10H11 cage system has undergone an unusual polytopal rearrangement to a nido-2-CB10H11 framework.


References

  1. (a) S. A. Batten, J. C. Jeffery, P. L. Jones, D. F. Mullica, M. D. Rudd, E. L. Sappenfield, F. G. A. Stone and A. Wolf, Inorg. Chem., 1997, 36, 2570 CrossRef CAS; (b) J. C. Jeffery, P. A. Jelliss and F. G. A. Stone, Organometallics, 1998, 17, 1402 CrossRef CAS; (c) I. Blandford, J. C. Jeffery, H. Redfearn, L. H. Rees, M. D. Rudd and F. G. A. Stone, J. Chem. Soc., Dalton Trans., 1998, 1669 RSC.
  2. G. D. Freiser, J. L. Little, J. C. Huffmann and L. J. Todd, Inorg. Chem., 1979, 18, 755 CrossRef.
  3. W. B. Hewer, A. E. True, P. N. Swepson and B. M. Hoffmann, Inorg. Chem., 1988, 27, 1474 CrossRef CAS and refs. therein.
  4. G. Ferguson, M. Parvez, J. A. McCurtian, O. N. Dhubhghaill, T. R. Spalding and D. Reed, J. Chem. Soc., Dalton Trans., 1987, 699 RSC; Faradoon, O. N. Dhubhghaill, T. R. Spalding, G. Ferguson, B. Kaitner, X. L. R. Fontaine and J. D. Kennedy, J. Chem. Soc., Dalton Trans., 1989, 1657 RSC.
  5. A. G. Orpen, L. Brammer, F. H. Allen, O. Kennard, D. Watson and R. Taylor, J. Chem. Soc., Dalton Trans., 1989, S1 RSC.
  6. CAChe Scientific, The Oxford Molecular Group, Oxford, 1994.
  7. C. A. Tolman, Chem. Rev., 1977, 77, 313 CrossRef CAS.
  8. S. A. Brew and F. G. A. Stone, Adv. Organomet. Chem., 1993, 35, 135 CAS.
  9. (a) D. F. Mullica, E. L. Sappenfield, F. G. A. Stone and S. F. Woollam, Organometallics, 1994, 13, 157 CrossRef CAS; (b) M. Gómez-Saso, D. F. Mullica, E. L. Sappenfield and F. G. A. Stone, Polyhedron, 1996, 15, 793 CrossRef CAS.
  10. T. Peymann, K. Kück and D. Gabel, Inorg. Chem., 1997, 36, 5138 CrossRef CAS.
  11. N. Petragnani, L. Torres and K. J. Wynne, J. Organomet. Chem., 1975, 92, 185 CrossRef CAS.
  12. E. H. S. Wong and M. F. Hawthorne, Inorg. Chem., 1978, 17, 2863 CrossRef CAS; R. E. King, S. B. Miller, C. B. Knobler and M. F. Hawthorne, Inorg. Chem., 1983, 22, 3548 CrossRef; H. C. Kang, S. S. Lee, C. B. Knobler and M. F. Hawthorne, Inorg. Chem., 1991, 30, 2024 CrossRef CAS; I. T. Chizhevsky, I. V. Pisareva, P. V. Petrovskii, V. I. Bregadze, A. I. Yanovsky, Yu. T. Struchkov, C. B. Knobler and M. F. Hawthorne, Inorg. Chem., 1993, 22, 3393 CrossRef.
  13. V. K. Jain, S. Kannan and R. Bohra, Polyhedron, 1992, 11, 1551 CrossRef CAS.
  14. D. M. Giolando, T. B. Rauchfuss and A. L. Rheingold, Inorg. Chem., 1987, 26, 1636 CrossRef CAS.
  15. M. F. Hawthorne, K. P. Callahan and R. J. Wiersema, Tetrahedron, 1974, 30, 1795 CrossRef CAS; C. B. Knobler, T. B. Marder, E. A. Mizusawa, R. G. Teller, J. A. Long, P. E. Behnken and M. F. Hawthorne, J. Am. Chem. Soc., 1984, 106, 2990 CrossRef CAS.
  16. S. A. Brew, N. Carr, J. C. Jeffery, M. U. Pilotti and F. G. A. Stone, J. Am. Chem. Soc., 1992, 114, 2203 CrossRef CAS; S. Li and F. G. A. Stone, Polyhedron, 1993, 12, 1689 CrossRef CAS.
  17. T. P. Hanusa, Polyhedron, 1982, 1, 663 CrossRef CAS.
  18. J. Plešek, T. Jelínek, E. Drdakova, S. Heřmánek and B. Stíbr, Collect. Czech. Commun., 1984, 49, 1559 Search PubMed.
  19. G. W. Parshall, Inorg. Synth., 1970, 12, 26 CAS.
  20. W. H. Knoth, J. L. Little, J. R. Lawrence, F. R. Scholer and L. J. Todd, Inorg. Synth., 1968, 11, 33 CAS.
  21. Bruker X-ray Instruments, Madison, WI, 1995.
Click here to see how this site uses Cookies. View our privacy policy here.