A new assembly of diiodine molecules at the triphenylphosphine sulfide template[hair space]

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

Massimiliano Arca, Francesco Demartin, Francesco A. Devillanova, Alessandra Garau, Francesco Isaia, Vito Lippolis and Gaetano Verani


Abstract

The new I2 adduct TPPS·3I2 (TPPS = triphenylphosphine sulfide) has been synthesized and characterised by X-ray diffraction on a single crystal. It consists of a TPPS·I2 1∶1 molecular adduct interacting with two further diiodine molecules in a “head to tail” sequence to give an overall TPPS·I2[hair space][hair space]· · ·[hair space][hair space]I2[hair space][hair space]· · ·[hair space][hair space]I2 arrangement in the asymmetric unit. Considering the I[hair space][hair space]· · ·[hair space][hair space]I interactions below 3.6 Å, five of the six iodine atoms of the asymmetric unit are arranged in infinite polycyclic ribbons. The iodine atoms, to which the TPPS molecules are connected, are almost perpendicular appendages on opposite sides of each ribbon. Weaker interactions between the ribbons give rise to unprecedented continuous stepped layers of diiodine molecules anchored to TPPS donor units. The structural features of TPPS·3I2 are discussed in comparison with those of the previously reported 2TPPS·3I2, TPPS·I2, TPPS·IBr and TPPS·ICl, and its FT-Raman spectrum compared with those of 2TPPS·3I2 and TPPS·I2. A re-examination of the equilibrium reaction between TPPS and I2 by 31P NMR confirms the formation of the 1∶1 adduct in CH2Cl2 solution and gives a formation constant value of 137 ± 11 dm3 mol–1.


References

  1. R. A. Zingaro and E. A. Meyers, Inorg. Chem., 1962, 1, 771 CrossRef CAS.
  2. R. A. Zingaro, R. E. McGlothlin and E. A. Meyers, J. Phys. Chem., 1962, 66, 2579 CrossRef.
  3. W. Tefteller, Jr. and R. A. Zingaro, Inorg. Chem., 1966, 5, 2151 CrossRef CAS.
  4. R. A. Zingaro and R. M. Hedges, J. Phys. Chem., 1961, 65, 1132 CrossRef CAS.
  5. R. A. Zingaro, Inorg. Chem., 1963, 2, 192 CrossRef CAS.
  6. W. W. Schweikert and E. A. Meyers, J. Phys. Chem., 1968, 72, 1561 CrossRef CAS; J. W. Bransford and E. A. Meyers, Cryst. Struct. Commun., 1978, 7, 697 Search PubMed.
  7. D. C. Apperley, N. Bricklebank, S. L. Burns and D. E. Hibbs, J. Chem. Soc., Dalton Trans., 1998, 1289 RSC.
  8. The results obtained by Bricklebank and co-workers7 are a clear example of how important the solvent can be in determining the nature of the final products in this type of reaction. Some other examples have been reported by us: F. Demartin, F. A. Devillanova, F. Isaia, V. Lippolis and G. Verani, Inorg. Chim. Acta, 1997, 255, 203 Search PubMed and refs. therein F. Bigoli, P. Deplano, M. L. Mercuri, M. A. Pellinghelli and E. F. Trogu, J. Chem. Res., 1993, (S) 90 CrossRef CAS.
  9. M. Arca, F. A. Devillanova, A. Garau, F. Isaia, V. Lippolis and G. Verani, Z. Anorg. Allg. Chem., 1998, 624, 745 CrossRef CAS.
  10. A. J. Blake, F. A. Devillanova, R. O. Gould, W.-S. Li, V. Lippolis, S. Parsons, C. Radek and M. Schröder, Chem. Soc. Rev., 1998, 27, 195 RSC.
  11. R. Faggiani, R. J. Gillespie, R. Kapoor, C. J. L. Lock and J. E. Vekris, Inorg. Chem., 1988, 27, 4350 CrossRef CAS.
  12. F. van Bolhuis, P. B. Koster and T. Migehelsen, Acta Crystallogr., 1967, 23, 90 CrossRef CAS.
  13. I. L. Karle, J. Chem. Phys., 1955, 23, 1739 CAS.
  14. S. C. Nyburg and C. H. Faerman, Acta Crystallogr., Sect. B, 1985, 41, 274 CrossRef.
  15. F. H. Herbstein and W. Schwotzer, (a)J. Am. Chem. Soc., 1984, 106, 2367; (b)Angew. Chem., Int. Ed. Engl., 1982, 21, 219 Search PubMed.
  16. F. Cristiani, F. A. Devillanova, F. Isaia, V. Lippolis, G. Verani and F. Demartin, Polyhedron, 1995, 14, 2937 CrossRef CAS.
  17. F. Cristiani, F. Demartin, F. A. Devillanova, F. Isaia, V. Lippolis and G. Verani, Inorg. Chem., 1994, 33, 6315 CrossRef CAS.
  18. P. W. Codding and K. A. Kerr, Acta Crystallogr., Sect. B, 1978, 34, 3785 CrossRef.
  19. M. C. Aragoni, M. Arca, F. Demartin, F. A. Devillanova, A. Garau, F. Isaia, V. Lippolis and G. Verani, Research Trends, 1999, in the press and refs. therein Search PubMed.
  20. L. Pauling, The Nature of the Chemical Bond, 3rd edn., Cornell University Press, Ithaca, NY, 1960 Search PubMed.
  21. F. Lux, R. Paetzold, J. Danel and L. Sobczyk, J. Chem. Soc., Faraday Trans. 2, 1975, 1610 RSC.
  22. S. Kaur and T. S. Lobana, J. Indian Chem. Soc., 1983, 60, 126 Search PubMed.
  23. M. Arca, F. Cristiani, F. A. Devillanova, A. Garau, F. Isaia, V. Lippolis, G. Verani and F. Demartin, Polyhedron, 1997, 16, 1983 CrossRef CAS.
  24. G. Carta, G. Crisponi and A. Lai, J. Magn. Reson., 1982, 48, 341 CAS.
  25. A. C. North, D. C. Phillips and F. S. Mathews, Acta Crystallogr., Sect. A, 1968, 24, 351 CrossRef.
  26. P. Main, S. J. Fiske, S. E. Hull, L. Lessinger, G. Germain, J. P. Declercq and M. N. Wolfson, MULTAN 80, Universities of York and Louvain, 1980.
  27. D. T. Cromer and J. T. Waber, International Tables for X-Ray Crystallography, Kynoch Press, Birmingham, 1974, vol. IV, Table 2.2B Search PubMed.
  28. D. T. Cromer, International Tables for X-Ray Crystallography, Kynoch Press, Birmingham, 1974, vol. IV, Table 2.3.1 Search PubMed.
  29. B. Frenz, Comput. Phys., 1988, 2, No. 3 (May/June) 42–8; B. Frenz, Crystallographic Computing 5, Oxford University Press, 1991, ch. 11, pp. 126–135 Search PubMed.
Click here to see how this site uses Cookies. View our privacy policy here.