Di(μ-oxo) Binuclear Manganese(III,IV) Poly(bipyridyl) Complexes Bearing Four Ruthenium(II) Photoactive Units: Synthesis, Characterization, and Photoinduced Electron-Transfer Properties

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Abstract
In order to model the photoinduced electron-transfer reactions from the manganese cluster to the photoactive P680 chlorophylls in photosystem II, three heterohexanuclear complexes, [Mn2III,IVO2{RuII(bpy)2(Ln)}4]11+ [bpy = 2,2‘-bipyridine, n = 2 (1a), 4 (1b), 6 (1c)], in which one MnIII,IV(μ-O)2 center is covalently linked to four RuII(bpy)3-like moieties by bridged bis(bipyridine) Ln ligands, have been synthesized and characterized. The electrochemical, photophysical, and photochemical properties of these complexes have been investigated in CH3CN. The cyclic voltammograms and rotating-disk electrode curves of the three complexes show the presence of two very close successive reversible oxidation processes corresponding to the Mn2III,IV/Mn2IV,IV and RuII/RuIII redox couples (estimated E1/2 ≈ 0.82 and 0.90 V, respectively). The lower potential of the Mn2III,IV subunit compared to those of the RuII moieties indicates that the RuIII species can act as an efficient oxidant toward the Mn2III,IV core. The two oxidized forms of the complexes [Mn2IV,IVO2{RuII(bpy)2(Ln)}4]12+ (2a−c) and [Mn2IV,IVO2{RuIII(bpy)2(Ln)}4]16+ (3a−c) obtained in good yields (>90% for 2a−c and >85% for 3a−c) by sequential electrolyses are very stable. Photophysical studies show that the 3MLCT excited state of the Ru(bpy)3 centers is moderately quenched by the Mn2III,IV(μ-O)2 core (15−25% depending on the length of the bridging alkyl chain). Nevertheless, this energy transfer can be easily short-circuited in the presence of an external irreversible electron acceptor like the (4-bromophenyl)diazonium cation, by an electron transfer leading, in a stepwise fashion, to the stable one- and five-electron-oxidized species 2a−c and 3a−c, respectively, also in good yields, under continuous irradiation of the solutions. Electro- and photoinduced oxidation experiments have been followed by UV−visible and electron paramagnetic resonance spectroscopy.

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