Photoinduced HydrogenAtom Transfer Catalysis withRuthenium Polypyridyl Coated-TiO₂ Nanoparticles for SelectiveC–C Bond Cleavage in a Lignin Model Compound

Ruthenium(II) polypyridine complexes have been widely studied for applications in dye-sensitized solar cells and artificial photosynthesis. Here, this work reports studies of intermolecular charge transfer from metal-to-ligand charge transfer (MLCT) excitation of Ru(II)-based chromophores onto TiO₂ nanoparticles to a hydrogen atom transfer (HAT) mediator and photocatalytic activation of HAT for cleavage of the C–C bond in the aryl ether linkages at room temperature. Initial studies demonstrated intermolecular energy/electron transfer among the photoexcited photocatalyst, bis(2,2′-bipyridine)(4,4′-dicarboxy-2,2′-bipyridine)Ru(II) (<b>RuC</b>) coated TiO₂ nanoparticles (RuC/TiO₂ NPs), the <i>N</i>-hydroxy-phthalimide (NHPI) HAT mediator, and the diol substrate 1-(3,4-dimethoxyphenyl)-2-(2-methoxyphenoxy)propane-1,3-diol (<b>LMC-ol</b>). Photophysical studies of RuC/TiO₂ NPs in the presence of NHPI/2,6-lutidine and <b>LMC-ol</b> exhibited a highly effective quenching for photoexcited RuC*/TiO₂ with K_SV = 7.21 × 10³ M^–1 compared to the lower quenching constant (K_SV ∼ 0.11 × 10³ M^–1) observed for RuC*/TiO₂ with only <b>LMC-ol</b> in acetonitrile solution. Under ambient temperature and aerobic conditions, the oxidative cleavage products of 3,4-dimethoxybenzaldehyde and 2-(2-methoxyphenoxy)-acetaldehyde from <b>LMC-ol</b> were obtained with the oxidized ketone product. This result indicates that the solar driven HAT-mediated process allows catalysis of the oxidative cleavage of C–C bonds in the aryl ether linkages via a one-pot cleavage reaction at room temperature. This photocatalytic system presents a possible approach to support lignin depolymerization targeting value-added aromatic chemicals and developing polymer degradation.