Wang Tao, Lawrence James, Sumi Naoya, Robles Roberto, Castro-Esteban Jesus, Rey Dulce, Mohammed Mohammed S G, Berdonces-Layunta Alejandro, Lorente Nicolas, Pérez Dolores, Peña Diego, Corso Martina, de Oteyza Dimas G
Donostia International Physics Center, San Sebastián, 20018, Spain.
Centro de Fisica de Materiales, CSIC-UPV/EHU, San Sebastián, 20018, Spain.
Phys Chem Chem Phys. 2021 May 12;23(18):10845-10851. doi: 10.1039/d1cp01212f.
The on-surface synthesis of non-planar nanographenes is a challenging task. Herein, with the aid of bond-resolving scanning tunneling microscopy (BRSTM) and density functional theory (DFT) calculations, we present a systematic study aiming at the fabrication of corannulene-based nanographenes via intramolecular cyclodehydrogenation on a Au(111) surface. The formation of non-planar targeted products is confirmed to be energetically unfavorable compared to the formation of planar/quasi-planar undesired competing monomer products. In addition, the activation of intermolecular coupling further inhibits the formation of the final targeted product. Although it was not possible to access the corannulene moiety by means of on-surface synthesis, partial cyclodehydrogenation of the molecular precursors was demonstrated.
非平面纳米石墨烯的表面合成是一项具有挑战性的任务。在此,借助键分辨扫描隧道显微镜(BRSTM)和密度泛函理论(DFT)计算,我们开展了一项系统研究,旨在通过在Au(111)表面进行分子内环脱氢反应制备基于碗烯的纳米石墨烯。与平面/准平面不期望的竞争单体产物的形成相比,非平面目标产物的形成在能量上被证实是不利的。此外,分子间偶联的活化进一步抑制了最终目标产物的形成。尽管无法通过表面合成获得碗烯部分,但已证明分子前体发生了部分环脱氢反应。