Theoretical Study of O–O Single Bond Formation in the Oxidation of Water by the Ruthenium Blue Dimer

• Published in: The journal of physical chemistry. A, Molecules, spectroscopy, kinetics, environment, & general theory Vol. 115; no. 27; pp. 8003 - 8016
• Main Authors: Bianco, Roberto, Hay, P. Jeffrey, Hynes, James T
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 14.07.2011
• Subjects: A: Molecular Structure, Quantum Chemistry, General Theory; Barriers; Bonding; Catalysis; Charge; Dimers; Free energy; Mathematical models; Models, Theoretical; Organometallic Compounds - chemistry; Oxidation; Oxidation-Reduction; Ruthenium - chemistry; Solvents; Thermodynamics; Water - chemistry
• ISSN: 1089-5639; 1520-5215
• DOI: 10.1021/jp200309d

The first key step in the oxidation of water to O2 by the oxidized species [(bpy)2(O)RuVORuV(O)(bpy)2]4+ of the Ru blue dimer is studied using density functional theory (DFT) and an explicit solvent treatment. In the model reaction system [L2(O)RuVORuV(O)L2]4+·(H2O)4·W76, the surrounding water solvent molecules W are described classically while the inner core reaction system is described quantum mechanically using smaller model ligands (L). The reaction path found for the O–O single bond formation involves a proton relay chain: direct participation of two water molecules in two proton transfers to yield the product [L2(HOO)RuIVORuIV(OH)L2]4+·(H2O)3·W76. The calculated ∼3 kcal/mol reaction free energy and ∼15 kcal/mol activation free energy barrier at 298 K are consistent with experiment. Structural changes and charge flow along the intrinsic reaction coordinate, the solvent’s role in the reaction barrier, and their significance for water oxidation catalysis are examined in detail.