Synthesis of a clathrate host for formamides, N-[2-(3,5-dinitrobenzoylamino)-6-methylphenyl]phthalimide, and analysis of the interactions in the host–guest complex

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Keiki Kishikawa, Ryota Takeuchi, Shigeo Kohmoto, Makoto Yamamoto, Kentaro Yamaguchi and Kazutoshi Yamada


Abstract

A clathrate host, N-[2-(3,5-dinitrobenzoylamino)-6-methylphenyl]phthalimide 1 is designed to achieve inclusion of N-substituted formamides. N,N-Dialkylformamides HCONR2 of various sizes 2a–e [2a: R = Me; 2b: R = Et; 2c: R = Pri; 2d: R2 = –(CH2)5–, 2e: R2 = –(CH2)2O(CH2)2–] and dimethyl sulfoxide have been included as the guests in a clathrate host 1, in the ratio 1∶1 in each case. The interaction between the host and guest has been investigated by X-ray analysis of complex 1·2c (1∶1). The phthalimide plane and the N-phenyl group are orthogonal, which makes a suitable space for recognition of the formamides.


References

  1. G. R. Desiraju, Angew. Chem., Int. Ed. Engl., 1995, 34, 2311 CrossRef CAS.
  2. F. Vögtle, Supramolecular Chemistry, Wiley, New York, 1991, ch. 5 pp. 171–193 Search PubMed.
  3. There are over 450 reports for DMF clathrates in the Cambridge Structural Database. The following are examples;; R. Hunter, R. H. Haueisen and A. Irving, Angew. Chem., Int. Ed. Engl., 1994, 33, 566 Search PubMed; D. J. Cram, M. E. Tanner and C. B. Knobler, J. Am. Chem. Soc., 1991, 113, 7717 CrossRef; E. Weber, S. Finge and I. Csoregh, J. Org. Chem., 1991, 56, 7281 CrossRef CAS; F. Toda, Tetrahedron Lett., 1968, 3695 CrossRef CAS.
  4. Kh. T. Sharipov, N. K. Makhmudovas, T. S. Khodashova, N. A. Parpiev and M. A. Porai-Kishits, Koord. Khim., 1982, 8, 117 Search PubMed; Kh. T. Sharipov, N. K. Makhmudovas, T. S. Khodashova and N. A. Parpiev, Zh. Strukt. Khim., 1982, 23, 170 Search PubMed; J. M. Adams, Acta Crystallogr., Sect. B, 1979, 35, 1084 CrossRef.
  5. M. Simard, J. Vaugeois and J. D. Wuest, J. Am. Chem. Soc., 1993, 115, 370 CrossRef CAS.
  6. A. A. Freer, J. H. Gall and D. D. MacNicol, J. Chem. Soc., Chem. Commun., 1982, 674 RSC.
  7. K. Nakamoto, M. Margoshes and R. E. Rundle, J. Am. Chem. Soc., 1955, 77, 6480 CrossRef CAS.
  8. A. Bondi, J. Phys. Chem., 1964, 68, 443.
  9. L. Pauling, The Nature of the Chemical Bond, Cornell University Press, Ithaca, New York, 3rd edn., 1960 Search PubMed.
  10. E. Weber, R. Pollex and M. Czugler, J. Org. Chem., 1992, 57, 4068 CrossRef CAS.
  11. M. E. Tanner, C. B. Knobler and D. J. Cram, J. Am. Chem. Soc., 1990, 112, 1659 CrossRef CAS.
  12. G. M. Sheldrick, Crystallographic Computing 3, ed. G. M. Sheldrick, C. Kruger and R. Goddard, Oxford University Press, Oxford, 1985, pp. 175–189 Search PubMed.
  13. P. T. Beurskens, G. Admiraal, G. Beurskens, W. P. Bosman, R. de Gelder, R. Israel and J. M. M. Smits, the DIRDIF-94 program system, Technical Report of the Crystallography Laboratory, University of Nijmegen, The Netherlands, 1994.
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