Key points are not available for this paper at this time.
We study the electrochemical, spectroscopic, and photocatalytic properties of a series of Ru (II) -Re (I) binuclear complexes linked by bridging ligands 1, 3-bis (4'-methyl-2, 2'bipyridinyl-4-yl) propan-2-ol (bpyC3bpy) and 4-methyl-4'-1, 10phenanthroline-5, 6-dimidazol-2-yl) bipyridine (mfibpy) and a tetranuclear complex in which three Re (CO) 3Cl moieties are coordinated to the central Ru using the bpyC3bpy ligands. In the bpyC3bpy binuclear complexes, 4, 4'-dimethyl-2, 2'-bipyridine (dmb) and 4, 4'-bis (trifluoromethyl) -2, 2'-bipyridine (CF32bpy), as well as 2, 2'-bipyridine (bpy), were used as peripheral ligands on the Ru moiety. Greatly improved photocatalytic activities were obtained only in the cases of RubpyC3bpyRe (CO) 3Cl32+ (RuRe3) and the binuclear complex (dmb) 2Ru (bpyC3bpy) Re (CO) 3Cl2+ (d2Ru-Re), while photocatalytic responses were extended further into the visible region. The excited state of ruthenium in all Ru-Re complexes was efficiently quenched by 1-benzyl-1, 4-dihydronicotinamide (BNAH). Following reductive quenching in the case of d2Ru-Re, generation of the one-electron-reduced (OER) species, for which the added electron resides on the Ru-bound bpy end of the bridging ligand bpyC3bpy, was confirmed by transient absorption spectroscopy. The reduced Re moiety was produced via a relatively slow intramolecular electron transfer, from the reduced Ru-bound bpy to the Re site, occurring at an exchange rate (DeltaG approximately 0). Electron transfer need not be rapid, since the rate-determining process is reduction of CO2 with the OER species of the Re site. Comparison of these results with those for other bimetallic systems gives us more general architectural pointers for constructing supramolecular photocatalysts for CO2 reduction.
Gholamkhass et al. (Thu,) studied this question.