Ultrathin Two‐Dimensional Metal–Organic Framework Nanosheets Based on a Halogen‐Substituted Porphyrin Ligand: Synthesis and Catalytic Application in CO2 Reductive Amination

Abstract

Ultrathin two-dimensional metal-organic framework nanosheets have emerged as a promising kind of heterogeneous catalysts. Herein, we report a series of 2D porphyrinic metal-organic framework nanosheets (X-PMOF, X=F, Cl, Br), which was prepared from the self-assembly of a halogen-based porphyrin ligand X-TCPP (X-TCPP=5-(4-halogenatedphenyl)-10,15,20-tris(4-carboxyphenyl)-porphyrin) and ZrCl4 in the presence of trifluoroacetic acid as the modulating reagent. The framework of X-PMOF possessed the ftw topology as in MOF-525. The lamellar X-PMOF nanosheets with the thickness of down to 4.5 nm were assembled and aggregated into a flower-like morphology. With the introduction of iridium(III) atoms into the porphyrin rings, the resultant X-PMOF(Ir) nanosheets were prepared by a similar method. Catalytic results show that Br-PMOF(Ir) nanosheets were efficient for CO2 reduction and aminolysis, giving rise to formamides in high yields under room temperature and atmospheric pressure, and can be recycled and reused for 3 runs. The total turnover number of Br-PMOF(Ir) after 3 runs was 1644 based on Ir. Mechanistic studies disclose that the high efficiency of Br-PMOF(Ir) nanosheets was ascribed to three factors, including the superior activation capability of iridium(III) porphyrin for Si-H bonds, more active sites on the external surfaces of Br-PMOF(Ir) nanosheets, and the defects caused by unsymmetrical porphyrin ligand that increased the framework's affinity towards CO2 .