We report a side chain-crowding strategy to direct the self-assembly of hydrogen-bonded semicarbazone macrocycles into porous organic frameworks with tunable curvatures and exceptional acetone uptake and selectivity. Three triangular macrocycles bearing isopropyl, isobutyl, and isopentyl side chains were synthesized and self-assembled through hydrogen-bonding arrays into planar, wrinkled, and square-octagonal wavy sheets, driven by steric congestion. After activation, the distorted frameworks retain permanent porosity and exhibit record-high acetone vapor uptake (up to 617 cm/g STP at 298 K) with high acetone/methanol selectivity (up to 7.
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