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A comparison between artificial and natural water oxidation
Stockholm University, Faculty of Science, Department of Physics. Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics.
Stockholm University, Faculty of Science, Department of Physics. Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics.
Stockholm University, Faculty of Science, Department of Physics. Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics.
2011 (English)In: Dalton Transactions, ISSN 1477-9226, E-ISSN 1477-9234, Vol. 40, no 42, 11296-11307 p.Article in journal (Refereed) Published
Abstract [en]

Two artificial water oxidation catalysts, the blue dimer and the Llobet catalyst, have been studied using hybrid DFT methods. The results are compared to those for water oxidation in the natural photosystem II enzyme. Studies on the latter system have now reached a high level of understanding, at present much higher than the one for the artificial systems. A recent high resolution X-ray structural investigation of PSII has confirmed the main features of the structure of the oxygen evolving complex (OEC) suggested by previous DFT cluster studies. The O-O bond formation mechanism suggested is of direct coupling (DC) type between an oxygen radical and a bridging oxo ligand. A similar DC mechanism is found for the Llobet catalyst, while an acid-base (AB) mechanism is preferred for the blue dimer. All of them require at least one oxygen radical. Full energy diagrams, including both redox and chemical steps, have been constructed illustrating similarities and differences to the natural system. Unlike previous DFT studies, the results of the present study suggest that the blue dimer is rate-limited by the initial redox steps, and the Llobet catalyst by O(2) release. The results could be useful for further improvement of the artificial systems.

Place, publisher, year, edition, pages
2011. Vol. 40, no 42, 11296-11307 p.
National Category
Organic Chemistry
Identifiers
URN: urn:nbn:se:su:diva-71014DOI: 10.1039/c1dt11323bISI: 000296024000028OAI: oai:DiVA.org:su-71014DiVA: diva2:483638
Note
4Available from: 2012-01-25 Created: 2012-01-25 Last updated: 2017-12-08Bibliographically approved

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Li, XichenSiegbahn, Per E. M.
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