Conformational and Enantiomeric Discrimination in Cyclodextrin Inclusion Compounds
Conference paper
Abstract
Cylodextrins open great possibi1ities for studying both the crysta1 structure and the spectroscopic properties in solution of the same compound. In the present paper new inc1usion compounds are studied. Two conformationaly labile molecu1es (cyclopentanone, bilirubin), the pheromone of the olive fly with chiral stab1e conformation and p- nitroani1ine with non linear optic properties are investigated.
Keywords
Circular Dichroism Inclusion Compound Fold Axis Linear Optic Property Chiroptical Property
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References
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© D. Reidel Publishing Company 1987