Hauptseite > Online First > Highly Structure‐Selective On‐Surface Synthesis of Isokekulene Versus Kekulene |
Journal Article | FZJ-2025-03408 |
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2025
Wiley-VCH
Weinheim
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Please use a persistent id in citations: doi:10.1002/anie.202509932
Abstract: The role of different facets of metal nanoparticles in steering reaction pathways is crucial for the design ofheterogeneous catalysts with superior selectivity. As a prominent class of reactions, transition-metal-catalyzed carbon-hydrogen (C─H) bond activation is widely used for the synthesis of base chemicals, modern organic materials, andpharmaceuticals. Here, we report orthogonal selectivity in intramolecular cyclodehydrogenation of a nonplanar cyclicprecursor steered by different facets of a copper single crystal. On the Cu(110) surface, the previously unknown cycloareneisokekulene forms with a high selectivity of 92%, whereas reaction on the Cu(111) surface exclusively yields kekulene(>99%). Combining scanning tunneling microscopy with CO-functionalized tips and density functional theory, we identifytwo adsorption geometries of the precursor, which react to the respective products. Isokekulene adopts two nonplanaradsorption configurations and exhibits strong molecule-substrate interactions, explaining its preferential formation onCu(110). This combined in-solution and on-surface synthesis approach represents an alternative route for the highlyselective synthesis of molecules that are challenging to synthesize and process via conventional methods.
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