Journal of the American Chemical Society · 2025 · 32 citations · 49 references
Natural SciencesChemistryMaterials ScienceCrystal StructureMaterials ChemistryOrganic ChemistryCrystal ChemistryCrystalline MaterialsCrystallographyStructure DeterminationX-ray CrystallographyX-ray DiffractionCovalent Organic FrameworksCrystal Structure-property RelationshipsInorganic CrystalsMolecular CrystalsOrganic CrystalsPorous CrystalsSingle-crystal DiffractionX-ray Diffraction Analysis
Determining the crystal structures of covalent organic frameworks (COFs) with atomic precision is pivotal for uncovering their properties and optimizing functionalities. However, the synthesis of high-quality single crystals of COFs suitable for X-ray diffraction analysis, especially chiral COFs (CCOFs), remains a formidable challenge. In this work, we report two three-dimensional (3D) CCOFs synthesized via imine condensation of tetrahedral tetraamine and tetraaldehydes derived from optically active 1,1'-biphenol phosphoryl chloride or thiophosphoryl chloride. Single crystals of varying sizes are obtained through either a low-temperature modulation strategy, yielding large crystals up to 100 μm, or a solvothermal method. The large single crystals are structurally characterized by single-crystal X-ray diffraction, achieving a resolution of 0.90 Å. These two CCOFs are isostructural and each features a 4-fold interpenetrated diamondoid open framework with all phosphoric acid groups periodically aligned within tubular helical channels, displaying enhanced Brønsted acidity compared to non-immobilized acids. The frameworks exhibit permanent porosity, chemical resistance in boiling water, 14 M NaOH, and 0.1 M HCl, and thermal stability up to 400 °C. Notably, these CCOFs serve as efficient and recyclable heterogeneous Brønsted acid catalysts in the asymmetric addition to aromatic aldehydes, enantioselective transfer hydrogenation of ketimines, and three-component direct asymmetric Mannich reactions involving aldimines and cyclic ketones, achieving good to high enantioselectivities (up to 99.5% ee) that surpass those obtained in analogous systems with homogeneous catalysts. This work represents the first successful demonstration of single-crystal structures of homochiral COFs, paving the way for in-depth investigations into structure-property relationships in enantioselective processes and facilitating the design of novel functional chiral organic materials.
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Single-crystal x-ray diffraction structures of covalent organic frameworks
Tianqiong Ma, Eugene A. Kapustin, Shawn X. Yin et al. · Science · 2018 · 1.3K citations