Inclusion compounds lattice energies

Soft and topologically adaptable supramolecular modules that allow host lattices to achieve dense packing through low-energy deformations, while retaining their inherent dimensionality and supramolecular connectivity, can facilitate the systematic design of molecular inclusion compounds. This is demonstrated by the ability to predict and maintain architectural control in a series of lamellar host frameworks. 

In most supramolecular structures, the temperature dependence of the characteristic dielectric relaxation time follows the Arrhenius equation, r = Toexp(A dip/ T). where tq is the preexponential factor that is often of the magnitude of the vibrational time scale and A dip is the activation energy of the dipolar process.The dipolar process of the host lattice and the trapped molecules follows this behavior, but A trapped molecules is less than that for the host lattice molecules. In ice ciathrates, the dipolar processes of the water molecules that form the host lattice and the guest molecules inside the cages of this lattice occur at widely different time scales. This allows for a reliable attribution of the dielectric spectra features to water molecules and to the guest molecules. As an example of the magnitude of the dielectric properties of supiainolecular structures, the data on selected ice clathrates and other inclusion compounds are summarized in Tables 1 and 2. 

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