Synthesizing Cr-Based Two-Dimensional Conjugated Metal-Organic Framework Through On-Surface Substitution Reaction

A single-layer Cr-3(HITP)(2) (HITP = 2,3,6,7,10,11-hexaiminotriphenylene) conjugated metal-organic framework (c-MOF) is synthesized under ultrahigh vacuum conditions by substituting Cr for Ni in Ni-3(HITP)(2) template. As revealed by low-temperature scanning tunneling microscopy and scanning tunneling spectroscopy, while codeposition of Cr atoms and 2,3,6,7,10,11-hexaaminotriphenylene precursors produces irregular branches, crystalline Cr-3(HITP)(2) frameworks are obtained by depositing Cr atoms to the Ni-3(HITP)(2) templates. The density functional theory calculations reveal that the binding energy between Cr and HITP ligands is much higher than that for Ni, which hampers the growth of crystalline Cr-3(HITP)(2) frameworks through direct coordination assembly but makes the substitution reaction energetically favorable. This work demonstrates a new strategy to prepare high-quality early-transition-metal-based c-MOFs under ultrahigh vacuum conditions.

Automated summary

A single-layer Cr-3(HITP)(2) conjugated metal-organic framework (c-MOF) is synthesized by substituting Cr for Ni in Ni-3(HITP)(2) templates under ultrahigh vacuum conditions. The deposition of Cr atoms onto the Ni-3(HITP)(2) templates leads to the formation of crystalline Cr-3(HITP)(2) frameworks, while codeposition of Cr atoms and 2,3,6,7,10,11-hexaaminotriphenylene precursors results in irregular branches. Density functional theory calculations demonstrate that the binding energy between Cr and HITP ligands is higher than that for Ni.