Non-stackable molecules assemble into porous crystals displaying concerted cavity-changing motions† † Electronic supplementary information (ESI) available: Experimental procedures and additional data (1H and 13C NMR spectra, FT-IR spectra, HR-MS) of the newly synthesized compounds. CCDC 1980363–1980368, 2048700, and 2048701. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/d1sc01163d
Ontology highlight
ABSTRACT: With small molecules, it is not easy to create large void spaces. Flat aromatics stack tightly, while flexible chains fold to fill the cavities. As an intuitive design to make open channels inside molecularly constructed solids, we employed propeller-shaped bicyclic triazoles to prepare a series of aromatic-rich three-dimensional (3D) building blocks. This modular approach has no previous example, but is readily applicable to build linear, bent, and branched arrays of non-stackable architectural motifs from existing flat aromatics by single-pot reactions. A letter H-shaped molecule thus prepared self-assembles into porous crystals, the highly unusual stepwise gas sorption behaviour of which prompted in-depth studies. A combination of single-crystal and powder X-ray diffraction analysis revealed multiple polymorphs, and sterically allowed pathways for their reversible interconversions that open and close the pores in response to external stimuli. Like non-collapsible open voids within stacks of steel H-beams, a non-covalent assembly of three-dimensional aromatics produces porous crystals. Concerted motions of the molecular H-beams open and close the cavities in response to external stimuli.
SUBMITTER: Kang T
PROVIDER: S-EPMC8115244 | biostudies-literature |
REPOSITORIES: biostudies-literature
ACCESS DATA