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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