The reaction of iodine with 9-methylacridine: formation of polyiodide salts and a charge-transfer complex

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Elizabeth L. Rimmer, Rosa D. Bailey, William T. Pennington and Timothy W. Hanks


Abstract

The reaction of iodine and 9-methylacridine in methylene chloride results not in the formation of a charge-transfer complex as with acridine, but in the iodine-rich salt [ICH2C13H8N–H]4(I8)(I5)2, 8, where a proton on the methyl group has been replaced by an iodine. In toluene, the reaction produces both a charge-transfer complex ICH2C13H8N–I2, 9, and a salt [CH3–acridine(H)]2(I7)(I5), 10. Polyiodide salt formation can be explained by the availability of a facile reaction pathway from the aryl radical cation which results from initial oxidation by I2.


References

  1. R. S. Mulliken, J. Am. Chem. Soc., 1952, 74, 811 CrossRef CAS.
  2. (a) C. Reid and R. S. Mulliken, J. Am. Chem. Soc., 1954, 76, 3869 CrossRef CAS; (b) P. A. Clark, T. J. Lerner, S. Hayes and S. G. Fischer, J. Phys. Chem., 1976, 16, 1809 CrossRef; (c) B. F. Levine and C. G. Bethea, J. Chem. Phys., 1977, 66, 1070 CrossRef CAS; (d) G. Maes, J. Mol. Struct., 1980, 61, 95 CrossRef CAS; (e) E. Yahagi, S. Matsumura, Y. Imai and K. Aida, Spectrochim. Acta, Part A, 1987, 43, 711 CrossRef; (f) N. S. Rao, G. B. Rao and D. Ziessow, Spectrochim. Acta, Part A, 1990, 46, 1107 CrossRef; (g) A. J. Sonnessa and J. M. Daisey, Spectrochim. Acta, Part A, 1976, 32, 465 CrossRef; (h) I. Uruska and H. Inerowicz, J. Solution Chem., 1980, 9, 97 CAS; (i) O. Hassel and C. Romming, Acta Chem. Scand., 1956, 10, 696 CAS.
  3. (a) S. Aronson, P. Epstein, D. B. Aronson and G. Wieder, J. Phys. Chem., 1982, 86, 1035 CrossRef CAS; (b) S. Aronson, S. B. Wilensky, T.-I. Yeh, D. Degraff and G. M. Weider, Can. J. Chem., 1986, 64, 2060 CAS; (c) Y. Danten, B. Guillot and Y. Guissani, J. Chem. Phys., 1992, 96, 3795 CrossRef CAS.
  4. O. Hassel and H. Hope, Acta Chem. Scand., 1961, 15, 407 CrossRef CAS.
  5. (a) R. D. Bailey and W. T. Pennnington, Acta Crystallogr., Sect. B, 1995, 51, 810 CrossRef; (b) R. D. Bailey, E. L. Rimmer, T. W. Hanks and W. T. Pennington, manuscript in preparation. A series of polyiodide salts of various azines and diazines will be reported Search PubMed.
  6. (a) K.-F. Tebbe and R. Buchem, Angew. Chem., 1997, 36, 1345 CAS; (b) A. L. Blake, F. A. Devillanova, R. O. Gould, W.-S. Li, V. Lippolis, S. Parsons, C. Radek and M. Schroder, Chem. Rev., 1998, 27, 195 CrossRef CAS; (c) for a recent description of the bonding in triodide anions, see G. A. Landrum, N. Goldberg and R. Hoffmann, J. Chem. Soc., Dalton Trans., 1997, 3605 Search PubMed.
  7. R. D. Bailey, M. L. Buchanan and W. T. Pennington, Acta Crystallogr., Sect. C, 1992, 48, 2259 CrossRef.
  8. E. L. Rimmer, R. D. Bailey, W. T. Pennington and T. W. Hanks, manuscript in preparation. The synthesis, structure and thermal properties of [acridine]2I6 and [chloroacridine]2I6 Search PubMed.
  9. S. Poul, Z. Naturforsch., Teil B, 1983, 38, 1535 Search PubMed.
  10. (a) R. D. Bailey, M. Grabarczyk, T. W. Hanks, E. M. Newton and W. T. Pennington, Electronic Conference on Trends in Organic Chemistry (ECTOC-1), eds. H. S. Rzepa and J. M. Goodman(CD-ROM), 1995, The Royal Society of Chemistry, see also http://www.ch.ic.ac.uk/ectoc/papers Search PubMed; (b) R. D. Bailey, G. W. Drake, M. Grabarczyk, T. W. Hanks, L. L. Hook and W. T. Pennington, J. Chem. Soc., Perkin Trans. 2, 1997, 2773 RSC; (c) R. D. Bailey, M. Grabarczyk, T. W. Hanks and W. T. Pennington, J. Chem. Soc., Perkin Trans. 2, 1997, 2781 RSC.
  11. (a) V. Ramamurth and K. Venkatesan, Chem. Rev., 1987, 87, 433 CrossRef CAS; (b) W. Jones, S. Ramdas, C. R. Theocharis, J. M. Thomas and N. W. Thomas, J. Phys. Chem., 1981, 85, 2594 CrossRef CAS.
  12. G. M. Sheldrick, SHELXTL-Plus, Version 4.2.1, Crystallographic Computing System, Siemens Analytical X-ray Instruments, Inc, Madison, WI, 1990.
  13. International Tables for X-ray Crystallography, vol. IV, The Kynoch Press, Birmingham, UK, 1974 Search PubMed.
  14. D. L. Glusker and A. Miller, J. Chem. Phys., 1957, 26, 331 CAS.
  15. O. Hassel, C. Romming and T. Tufte, Acta Chem. Scand., 1961, 15, 967 CAS.
  16. (a) S. S. Barton and R. H. Pottier, J. Chem. Soc., Perkin Trans. 2, 1984, 731 RSC; (b) J. N. Chaudhuri and S. Basu, Trans. Faraday Soc., 1959, 53, 898 RSC ; also see ref. 2d.
  17. (a) L. M. Tolbert, R. K. Khanna, A. E. Popp, L. Gelbaum and L. A. Bottomley, J. Am. Chem. Soc., 1990, 112, 2373 CrossRef CAS; (b) S. R. Sirimanne, Z. Li, D. R. VanDerveer and L. M. Tolbert, J. Am. Chem. Soc., 1991, 113, 1766 CrossRef CAS; (c) L. M. Tolbert, Z. Li, S. R. Sirimanne and D. G. VanDerveer, J. Org. Chem., 1997, 62, 3927 CrossRef CAS.
  18. L. Pauling, The Nature of the Chemical Bond, 3rd edn., Cornell University Press, New York, 1960, p. 260 Search PubMed.
  19. A. I. Vogel, Textbook of Practical Organic Chemistry, 5th edn., eds. B. S. Furniss, A. J. Hannaford, P. W. G. Smith and A. R. Tatchell, Longman Scientific and Technical, Essex, 1989 Search PubMed.
  20. A. Markovac, C. L. Stevens, A. B. Ash and B. E. Hackley, Jr., J. Org. Chem., 1970, 35, 841 CrossRef CAS.
  21. For example, see: (a) D. Rehm and A. Weller, Israel J. Chem., 1970, 8, 259 Search PubMed; (b) A. M. de. P. Nicholas and D. R. Arnold, Can. J. Chem., 1982, 60, 2165 CAS; (c) F. G. Bordwell, J.-P. Chen and M. J. Bausch, J. Am. Chem. Soc., 1988, 110, 2867 CrossRef CAS.
  22. D. B. Morse, T. B. Rauchfuss and S. R. Wilson, J. Am. Chem. Soc., 1990, 112, 1860 CrossRef CAS.
  23. P. C. Junk, L. R. MacGillivray, M. T. May, K. D. Robinson and J. L. Atwood, Inorg. Chem., 1995, 34, 5395 CrossRef CAS.
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