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Quantum Tunneling Mediated Interfacial Synthesis of a Benzofuran Derivative
Authors:Tobias Paintner  Jonas Bjrk  Ping Du  Svetlana Klyatskaya  Mateusz Paszkiewicz  Raphael Hellwig  Martin Uphoff  Murat A ner  Edoardo Cuniberto  Peter S Deimel  Yi‐Qi Zhang  Carlos‐Andres Palma  Francesco Allegretti  Mario Ruben  Johannes V Barth  Florian Klappenberger
Institution:Tobias Paintner,Jonas Björk,Ping Du,Svetlana Klyatskaya,Mateusz Paszkiewicz,Raphael Hellwig,Martin Uphoff,Murat A. Öner,Edoardo Cuniberto,Peter S. Deimel,Yi‐Qi Zhang,Carlos‐Andres Palma,Francesco Allegretti,Mario Ruben,Johannes V. Barth,Florian Klappenberger
Abstract:Reaction pathways involving quantum tunneling of protons are fundamental to chemistry and biology. They are responsible for essential aspects of interstellar synthesis, the degradation and isomerization of compounds, enzymatic activity, and protein dynamics. On‐surface conditions have been demonstrated to open alternative routes for organic synthesis, often with intricate transformations not accessible in solution. Here, we investigate a hydroalkoxylation reaction of a molecular species adsorbed on a Ag(111) surface by scanning tunneling microscopy complemented by X‐ray electron spectroscopy and density functional theory. The closure of the furan ring proceeds at low temperature (down to 150 K) and without detectable side reactions. We unravel a proton‐tunneling‐mediated pathway theoretically and confirm experimentally its dominant contribution through the kinetic isotope effect with the deuterated derivative.
Keywords:Hydroalkoxylierungen  Oberflä  chensynthese  Quantentunneln  Rastertunnelmikroskopie    ntgenspektroskopie
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