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Conformational and enantiomeric discrimination in cyclodextrin inclusion compounds

  • Cyclodextrins
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Abstract

Cyclodextrins open great possibilities for studying both the crystal structure and the spectroscopic properties in solution of the same compound. In the present paper new inclusion compounds are studied. Two conformatonaly labile molecules (cyclopentanone, bilirubin), the pheromone of the olive fly with chiral stable conformation and p-nitroaniline with non linear optic properties are investigated.

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Authors and Affiliations

  1. Laboratoire de Physique centre Pharmaceutique, Universite Paris-Sud, 92290, Chatenay-Malabry

    G. Tsoucaris, G. Le Bas, N. Rysanek & F. Villain

Authors
  1. G. Tsoucaris
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  2. G. Le Bas
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  3. N. Rysanek
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  4. F. Villain
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Tsoucaris, G., Le Bas, G., Rysanek, N. et al. Conformational and enantiomeric discrimination in cyclodextrin inclusion compounds. Journal of Inclusion Phenomena 5, 77–84 (1987). https://doi.org/10.1007/BF00656407

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  • DOI: https://doi.org/10.1007/BF00656407

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