Abstract
The inclusion compounds of binaphthol with three isomers of xylidine have been studied in terms of their structures and infra-red spectra. Competition experiments show that the selectivity of enclathration follows the trend: 2,6-xylidine > 2,3-xylidine ≈ 3,5-xylidine. The kinetics of desolvation have been analysed and the activation energies established.

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