▎ 摘　　要

Selective control on the topology of low-dimensional covalent organic nanostructures in on-surface synthesis has been challenging. Herein, with combined scanning tunneling microscopy (STM) and X-ray photoelectron spectroscopy (XPS), we report a successful topology-selective coupling reaction on the Cu(111) surface by tuning the thermal annealing procedure. The precursor employed is 1,3,5-tris(2-bromophenyl)benzene (TBPB), for which Ullmann coupling is impeded due to the intermolecular steric hindrance. Instead, its chemisorption on the Cu(111) substrate has triggered the ortho CH bond activation and the following dehydrogenative coupling at room temperature (RT). In the slow annealing experimental procedure, the monomers have been preorganized by their self-assembly at RT, which enhances the formation of dendritic structures upon further annealing. However, the chaotic chirality of dimeric products (obtained at RT) and hindrance from dense molecular island make the fabrication of high-quality porous two-dimensional nanostructures difficult. In sharp contrast, direct deposition of TBPB molecules on a hot surface led to the formation of ordered porous graphene nanoribbons and nanoflakes, which is confirmed to be the energetically favorable reaction pathway through density functional theory-based thermodynamic calculations and control experiments. This work demonstrates that different thermal treatments could have a significant influence on the topology of covalent products in on-surface synthesis and presents an example of the negative effect of molecular self-assembly to the ordered covalent nanostructures.