Empa, Swiss Federal Laboratories for Materials Science and Technology, nanotech@surfaces Laboratory, 8600 Dübendorf, Switzerland.
Max Planck Institute for Polymer Research, 55128 Mainz, Germany.
J Am Chem Soc. 2020 Jul 15;142(28):12046-12050. doi: 10.1021/jacs.0c05268. Epub 2020 Jul 2.
Coronoids, polycyclic aromatic hydrocarbons with geometrically defined cavities, are promising model structures of porous graphene. Here, we report the on-surface synthesis of C168 and C140 coronoids, referred to as [6]- and [5]coronoid, respectively, using 5,9-dibromo-14-phenylbenzo[]tetraphene as the precursor. These coronoids entail large cavities (>1 nm) with inner zigzag edges, distinct from their outer armchair edges. While [6]coronoid is planar, [5]coronoid is not. Low-temperature scanning tunneling microscopy/spectroscopy and noncontact atomic force microscopy unveil structural and electronic properties in accordance with those obtained from density functional theory calculations. Detailed analysis of ring current effects identifies the rings with the highest aromaticity of these coronoids, whose pattern matches their Clar structure. The pores of the obtained coronoids offer intriguing possibilities of further functionalization toward advanced host-guest applications.
冠状物是具有几何定义空腔的多环芳烃,是多孔石墨烯的有前途的模型结构。在这里,我们报告了使用 5,9-二溴-14-苯基苯并[]四苯作为前体,在表面上合成 C168 和 C140 冠状物,分别称为[6]-和[5]冠状物。这些冠状物具有较大的空腔(>1nm),具有内部锯齿边缘,与外部扶手椅边缘不同。虽然[6]冠状物是平面的,但[5]冠状物不是。低温扫描隧道显微镜/光谱和非接触原子力显微镜揭示了与密度泛函理论计算所得结果一致的结构和电子性质。对环电流效应的详细分析确定了这些冠状物中具有最高芳香度的环,其模式与它们的 Clar 结构相匹配。所得冠状物的孔为进一步功能化提供了有趣的可能性,以实现先进的主客体应用。