The dynamic behavior of supramolecular organic frameworks (SOFs) based on the rigid tetra‐4‐(4‐pyridyl)phenylmethane (TPPM) organic tecton has been elucidated through 3D electron diffraction, X‐ray powder diffraction and differential scanning calorimetry (DSC) analysis. The SOF undergoes a reversible single‐crystal‐to‐single‐crystal transformation when exposed to vapours of selected organic solvents, moving from a closed structure with isolated small voids to an expanded structure with solvated channels along the b axis. The observed selectivity is dictated by the fitting of the guest in the expanded SOF, following the degree of packing coefficient. The effect of solvent uptake on TPPM solid‐state fluorescence was investigated, evidencing a significant variation in the emission profile only in the presence of chloroform.

No abstract

Auxetics are materials characterized by a negative Poisson’s ratio (NPR), an uncommon mechanical behavior corresponding to a transversal deformation tendency opposite to the traditional materials. Here we present the first example of a 3D synthetic molecular auxetic polymer, obtained by embedding a conformationally expandable cavitand as crosslinker into a rigid polymer of intrinsic microporosity (PIM). The rigidity and microporosity of the polymeric matrix are pivotal to maximize the expansion effect of the cavitand that, under mechanical stress, can assume two different conformations: a compact vase one and an extended kite form. The auxetic behavior and the corresponding NPR of the proposed material is predicted by a specific micromechanical model that considers the cavitand volume expansion ratio, the fraction of the cavitand crosslinker in the polymer, and the mechanical characteristics of the polymer backbone. The reversible auxetic behavior of the material is experimentally verified via Digital Image Correlation technique (DIC) performed during the mechanical tests on films obtained by blending the auxetic crosslinked polymer with pristine PIM. Two specific control experiments prove that the mechanically driven conformational expansion of the cavitand crosslinker is the sole responsible of the observed NPR of the polymer.