Urgel José I, Di Giovannantonio Marco, Gandus Guido, Chen Qiang, Liu Xunshan, Hayashi Hironobu, Ruffieux Pascal, Decurtins Silvio, Narita Akimitsu, Passerone Daniele, Yamada Hiroko, Liu Shi-Xia, Müllen Klaus, Pignedoli Carlo A, Fasel Roman
Empa, Swiss Federal Laboratories for Materials Science and Technology nanotech@surfaces Laboratory, 8600, Dübendorf, Switzerland.
Max Planck Institute for Polymer Research, 55128, Mainz, Germany.
Chemphyschem. 2019 Sep 17;20(18):2360-2366. doi: 10.1002/cphc.201900283. Epub 2019 May 14.
On-surface synthesis is a unique tool for growing low-dimensional carbon nanomaterials with precise structural control down to the atomic level. This novel approach relies on carefully designed precursor molecules, which are deposited on suitable substrates and activated to ultimately form the desired nanostructures. One of the most applied reactions to covalently interlink molecular precursors is dehalogenative aryl-aryl coupling. Despite the versatility of this approach, many unsuccessful attempts are also known, most of them associated to the poor capability of the activated precursors to couple to each other. Such failure is often related to the steric hindrance between reactants, which may arise due to their coplanarity upon adsorption on a surface. Here, we propose a copolymerization approach to overcome the limitations that prevent intermolecular homocoupling. We apply the strategy of using suitable linkers as additional reactants to the formation of fully conjugated polycyclic nanowires incorporating non-benzenoid rings.
表面合成是一种独特的工具,用于生长具有精确结构控制直至原子水平的低维碳纳米材料。这种新颖的方法依赖于精心设计的前驱体分子,这些分子沉积在合适的基底上并被激活,最终形成所需的纳米结构。用于共价连接分子前驱体的最常用反应之一是脱卤芳基-芳基偶联。尽管这种方法具有通用性,但也有许多不成功的尝试,其中大多数与活化前驱体彼此偶联的能力差有关。这种失败通常与反应物之间的空间位阻有关,这可能是由于它们吸附在表面时的共面性所致。在这里,我们提出了一种共聚方法来克服阻止分子间均偶联的限制。我们将使用合适的连接体作为额外反应物的策略应用于包含非苯环的完全共轭多环纳米线的形成。