Supramolecular Cages Based on a Silver Complex as Adaptable Hosts for Poly-Aromatic Hydrocarbons.

Abstract

In this work, an L-shaped silver complex, AgLClO4 (L = 2,3-bis[3-(pyridin-2-yl)-1H-pyrazol-1-yl·methyl]quinoxaline), M, is found to be adaptable enough to host a range of medium and large aromatic hydrocarbons including several polycyclic aromatic hydrocarbons (PAHs). The transformation of M from as-synthesized closed (nonporous) crystalline to at least three types of open phase structures in the presence of different aromatic hydrocarbons enables the adaptable binding of M to these aromatics. In essence, M can rearrange its cavities to fit the different sizes and shapes of the guest molecules in the manner that is infeasible with cage compounds or coordination networks. Single-crystal and powder X-ray diffraction confirm the adaptable structures of the resulting host-guest complexes, M·nG (G= guest, n= 0.5 or 0.75). Detailed 1D and 2D nuclear magnetic resonance spectra, along with the fluorescence spectroscopy, reveal that the host-guest complexes feature similar chemical compositions in the solution, but are in the states of rapid exchange in and outside the cages. Such an adaptability of M provides insights into the strength of host-guest interactions and enables a new class of adsorptive molecular materials that can bind a large number of aromatics, specifically PAHs.