Structures of the inclusion compounds formed between the host compound 1, 1-bis(4-hydroxyphenyl)cyclohexane and selected lutidine isomers have been elucidated. The activation energies and kinetics of desolvation for the complexes were determined. Competition experiments were performed to investigate preferential enclathration. Lattice energy calculations explain the results of the competition experiments.
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Caira et al. (1998) studied this question.
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