The design of unsaturated nonprecious metal complexes with high catalytic performance for photochemical CO reduction is still an important challenge. In this paper, four coordinatively unsaturated Co-salen complexes - were explored in situ using -phenylenediamine derivatives and 5-methylsalicylaldehyde as precursors of the ligands in -. It was found that complex , bearing a nitro substituent (-NO) on the aromatic ring of the salen ligand, exhibits the highest photochemical performance for visible-light-driven CO-to-CO conversion in a water-containing system, with TON and CO selectivity values of 5300 and 96%, respectively.
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