Two-dimensional metal–organic networks (2D MONs)
having
heterogeneous coordination nodes (HCNs) could exhibit excellent performance
in catalysis and optoelectronics because of the unbalanced electron
distribution of the coordinating metals. Therefore, the design and
construction of 2D MONs with HCNs are highly desirable but remain
challenging. Here, we report the construction of 2D organometallic
coordination networks with an organic Kagome lattice and a semiregular
metal lattice on Au(111) via the in situ formation of HCNs. Using
a bifunctional precursor 1,4-dibromo-2,5-diisocyanobenzene, the coordination
of isocyano with Au adatom on a room-temperature Au(111) yielded metal–organic
coordination chains with isocyano-Au-isocyano nodes. In contrast,
on a high-temperature Au(111), a selective debromination/coordination
cascade reaction occurred, affording 2D organometallic coordination
networks with phenyl-Au-isocyano nodes. By combining scanning tunneling
microscopy and density functional theory calculations, we determined
the structures of coordination products and the nature of coordination
nodes, demonstrating a thermodynamically favorable pathway for forming
the phenyl-Au-isocyano nodes.