Björk Jonas, Sánchez-Sánchez Carlos, Chen Qiang, Pignedoli Carlo A, Rosen Johanna, Ruffieux Pascal, Feng Xinliang, Narita Akimitsu, Müllen Klaus, Fasel Roman
Department of Physics, Chemistry and Biology, IFM, Linköping University, 58183, Linköping, Sweden.
nanotech@surfaces Laboratory, Empa, Swiss Federal Laboratories for Materials Science and Technology, Überlandstrasse 129, 8600, Dübendorf, Switzerland.
Angew Chem Int Ed Engl. 2022 Dec 5;61(49):e202212354. doi: 10.1002/anie.202212354. Epub 2022 Nov 8.
Dehydrogenation reactions are key steps in many metal-catalyzed chemical processes and in the on-surface synthesis of atomically precise nanomaterials. The principal role of the metal substrate in these reactions is undisputed, but the role of metal adatoms remains, to a large extent, unanswered, particularly on gold substrates. Here, we discuss their importance by studying the surface-assisted cyclodehydrogenation on Au(111) as an ideal model case. We choose a polymer theoretically predicted to give one of two cyclization products depending on the presence or absence of gold adatoms. Scanning probe microscopy experiments observe only the product associated with adatoms. We challenge the prevalent understanding of surface-assisted cyclodehydrogenation, unveiling the catalytic role of adatoms and their effect on regioselectivity. The study adds new perspectives to the understanding of metal catalysis and the design of on-surface synthesis protocols for novel carbon nanomaterials.
脱氢反应是许多金属催化化学过程以及原子精确纳米材料表面合成中的关键步骤。金属底物在这些反应中的主要作用是无可争议的,但金属吸附原子的作用在很大程度上仍未得到解答,尤其是在金底物上。在这里,我们通过研究在Au(111)上的表面辅助环化脱氢反应作为一个理想的模型案例来讨论它们的重要性。我们选择一种理论上预测根据金吸附原子的存在与否会产生两种环化产物之一的聚合物。扫描探针显微镜实验仅观察到与吸附原子相关的产物。我们挑战了对表面辅助环化脱氢反应的普遍理解,揭示了吸附原子的催化作用及其对区域选择性的影响。该研究为理解金属催化以及新型碳纳米材料的表面合成方案设计增添了新的视角。