Near-infrared light photocatalysis enabled by a ruthenium complex-integrated metal–organic framework via two-photon absorption

Photocatalysis under UV/visible light irradiation has emerged as one of the green methodologies for solar energy utilization and organic synthesis. These photocatalytic processes are typically initiated by one-photon-absorbing metal complexes or organic dyes. Nevertheless, the intrinsic restrictions of UV/visible light irradiation, such as shallow penetration in reaction solutions, competing absorption by substrates, and limited coverage of the solar spectrum, call for the development of innovative photocatalysts functioning under longer wavelength irradiation. Herein, we report a ruthenium complex containing a metal-organic framework, MOF-Ru1, which can drive diverse organic reactions under 740 nm light irradiation following the two-photon absorption (TPA) process. Various organic transformations such as energy transfer, reductive, oxidative, and redox neutral reactions were realized using this heterogeneous hybrid photocatalyst. Overall, MOF-Ru1 represents an intriguing TPA photocatalyst active under near-infrared light irradiation, paving a way for the efficient utilization of low-energy light and convenient photocatalyst recycling because of phase separation. [Display omitted] •Ru complexes with π-conjugation ligands show two-photon absorption of NIR photons•Hybrid MOF-Ru has NIR light-driven photocatalytic performance with recyclability•A variety of organic reactions were photocatalyzed by MOF-Ru under 740 nm irradiation Chemistry; Chemical reaction; Catalysis; Optical Materials