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Updated: Jun 4, 2025
Ultrahigh Density Array of Vertically Aligned Small-molecular Organic Nanowires on Arbitrary Substrates
Published on: June 18, 2013
Spatially Confined Construction of Ultrasmall Pd Clusters Within Nitro-Bonded Covalent Organic Frameworks for
Xujiao Ma1, Zhong Zhang1, Die Zhao2
1School of Chemistry, Dalian University of Technology, Dalian, 116024, China.
Abstract:
Confinement of metal species in porous supports is an effective strategy to optimize hydrogenation performance ascribing to tunable nanopore environments. However, only focusing on the electronic structure modulation for metal species has limited the design of improved catalysts. Herein, spatial confinement strategy is reported for constructing ultrasmall metal clusters in nitro-bonded COF (M@TpPa-NO2, M = Pd, Pt, Ru, Rh, Ir). Thereinto, Pd@TpPa-NO2 can achieve efficient co-catalytic alkyne semi-hydrogenation by the organic nitro units and the Pd clusters, with an outstanding phenylacetylene hydrogenation activity of TOF = 13756 h-1 and a high 94% styrene selectivity under 25 °C and 1 bar H2. In situ diffuse reflectance infrared Fourier transform spectroscopy and density functional theory calculations confirm that the H2 dissociation occurs at Pd clusters and the nitro groups accept spilled H atoms for subsequent semi-hydrogenation. The facile styrene desorption from TpPa-NO2 support contributes to a high semi-hydrogenation selectivity. This work provides new perspectives for designing efficient catalysts with overcoming the activity-selectivity trade-off in selective hydrogenation reactions.
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