Synthesis, Protonation, and Reduction of Ruthenium–Peroxo Complexes with Pendent Nitrogen Bases

Journal Article · Mon Oct 15 04:00:00 EDT 2012 · Inorganic Chemistry

DOI:https://doi.org/10.1021/ic3013987· OSTI ID:1054467

Tronic, Tristan A.; Kaminsky, Werner; Coggins, Michael K.; Mayer, James M.

Cyclopentadienyl and pentamethylcyclopentadienyl ruthenium(II) complexes have been synthesized with cyclic (RPCH₂NR'CH₂)₂ ligands, with the goal of using these [Cp^R"Ru(P^R₂N^R'₂)]⁺ complexes for catalytic O₂ reduction to H₂O (R = t-butyl, phenyl; R' = benzyl, phenyl; R" = methyl, H). In each compound, the Ru is coordinated to the two phosphines, positioning the amines of the ligand in the second coordination sphere where they may act as proton relays to a bound dioxygen ligand. The phosphine, amine, and cyclopentadienyl substituents have been systematically varied in order to understand the effects of each of these parameters on the properties of the complexes. These Cp^R"Ru(P^R₂N^R'₂)⁺ complexes react with O₂ to form η²-peroxo complexes, which have been characterized by NMR, IR, and X-ray crystallography. The peak reduction potentials of the O₂ ligated complexes have been shown by cyclic voltammetry to vary as much as 0.1 V upon varying the phosphine and amine. In the presence of acid, protonation of these complexes occurs at the pendent amine, forming a hydrogen bond between the protonated amine and the bound O₂. The ruthenium–peroxo complexes decompose upon reduction, precluding catalytic O₂ reduction. Finally, the irreversible reduction potentials of the protonated O₂ complexes depend on the basicity of the pendent amine, giving insight into the role of the proton relay in facilitating reduction.

• Research Organization: Pacific Northwest National Laboratory (PNNL), Richland, WA (US)
• Sponsoring Organization: USDOE
• DOE Contract Number: AC05-76RL01830
• OSTI ID: 1054467
• Report Number(s): PNNL-SA-88856; KC0307010
• Journal Information: Inorganic Chemistry, Journal Name: Inorganic Chemistry Journal Issue: 20 Vol. 51; ISSN 0020-1669
• Publisher: American Chemical Society (ACS)
• Country of Publication: United States
• Language: English