Isolation of a Ru(IV) side-on peroxo intermediate in the water oxidation reaction

被引:48
作者
Casadevall, Carla [1 ]
Martin-Diaconescu, Vlad [1 ]
Browne, Wesley R. [2 ]
Fernandez, Sergio [1 ]
Franco, Federico [1 ]
Cabello, Noemi [1 ]
Benet-Buchholz, Jordi [1 ]
Lassalle-Kaiser, Benedikt [3 ]
Lloret-Fillol, Julio [1 ,4 ]
机构
[1] Barcelona Inst Sci & Technol, Inst Chem Res Catalonia ICIQ, Tarragona, Spain
[2] Univ Groningen, Fac Sci & Engn, Stratingh Inst Chem, Mol Inorgan Chem, Groningen, Netherlands
[3] Synchrotron SOLEIL, Gif Sur Yvette, France
[4] Catalan Inst Res & Adv Studies ICREA, Barcelona, Spain
关键词
RUTHENIUM; COMPLEXES; CATALYST; BOND;
D O I
10.1038/s41557-021-00702-5
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The electrons that nature uses to reduce CO2 during photosynthesis come from water oxidation at the oxygen-evolving complex of photosystem II. Molecular catalysts have served as models to understand its mechanism, in particular the O-O bond-forming reaction, which is still not fully understood. Here we report a Ru(IV) side-on peroxo complex that serves as a 'missing link' for the species that form after the rate-determining O-O bond-forming step. The Ru(IV) side-on peroxo complex (eta(2)-1(IV)-OO) is generated from the isolated Ru(IV) oxo complex (1(IV)=O) in the presence of an excess of oxidant. The oxidation (IV) and spin state (singlet) of eta(2)-1(IV)-OO were determined by a combination of experimental and theoretical studies. O-18- and H-2-labelling studies evidence the direct evolution of O-2 through the nucleophilic attack of a H2O molecule on the highly electrophilic metal-oxo species via the formation of eta(2)-1(IV)-OO. These studies demonstrate water nucleophilic attack as a viable mechanism for O-O bond formation, as previously proposed based on indirect evidence.
引用
收藏
页码:800 / +
页数:6
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