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Efficient photochemical water oxidation by a dinuclear molecular ruthenium complex
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.ORCID-id: 0000-0002-6089-5454
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi. Huazhong University of Science & Technology, People's Republic of China.ORCID-id: 0000-0002-8989-6928
Stockholms universitet, Naturvetenskapliga fakulteten, Institutionen för organisk kemi.
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2015 (Engelska)Ingår i: Chemical Communications, ISSN 1359-7345, E-ISSN 1364-548X, Vol. 51, nr 10, s. 1862-1865Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Herein is described the preparation of a dinuclear molecular Ru catalyst for H2O oxidation. The prepared catalyst mediates the photochemical oxidation of H2O with an efficiency comparable to state-of-the-art catalysts.

Ort, förlag, år, upplaga, sidor
Royal Society of Chemistry, 2015. Vol. 51, nr 10, s. 1862-1865
Nationell ämneskategori
Kemi
Forskningsämne
organisk kemi
Identifikatorer
URN: urn:nbn:se:su:diva-114259DOI: 10.1039/c4cc08606fISI: 000348213200020PubMedID: 25525645OAI: oai:DiVA.org:su-114259DiVA, id: diva2:798474
Forskningsfinansiär
Knut och Alice Wallenbergs StiftelseVetenskapsrådetCarl Tryggers stiftelse för vetenskaplig forskning Energimyndigheten
Anmärkning

AuthorCount:8;

Tillgänglig från: 2015-03-26 Skapad: 2015-02-25 Senast uppdaterad: 2020-03-05Bibliografiskt granskad
Ingår i avhandling
1. Development of Ruthenium Catalysts for Water Oxidation
Öppna denna publikation i ny flik eller fönster >>Development of Ruthenium Catalysts for Water Oxidation
2016 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

An increasing global energy demand requires alternative fuel sources. A promising method is artificial photosynthesis. Although, the artificial processes are different from the natural photosynthetic process, the basic principles are the same, i.e. to split water and to convert solar energy into chemical energy. The energy is stored in bonds, which can at a later stage be released upon combustion. The bottleneck in the artificial systems is the water oxidation. The aim of this research has been to develop catalysts for water oxidation that are stable, yet efficient. The molecular catalysts are comprised of organic ligands that ultimately are responsible for the catalyst structure and activity. These ligands are often based on polypyridines or other nitrogen-containing aromatic compounds. This thesis describes the development of molecular ruthenium catalysts and the evaluation of their ability to mediate chemical and photochemical oxidation of water. Previous work from our group has shown that the introduction of negatively charged groups into the ligand frameworks lowers the redox potentials of the metal complexes. This is beneficial as it makes it possible to drive water oxidation with [Ru(bpy)3]3+-type oxidants (bpy = 2,2’-bipyridine), which can be photochemically generated from the corresponding [Ru(bpy)3]2+ complex. Hence, all the designed ligands herein contain negatively charged groups in the coordination site for ruthenium.

The first part of this thesis describes the development of two mononuclear ruthenium complexes and the evaluation of these for water oxidation. Both complexes displayed low redox potentials, allowing for water oxidation to be driven either chemically or photochemically using the mild one-electron oxidant [Ru(bpy)3]3+.

The second part is a structure–activity relationship study on several analogues of mononuclear ruthenium complexes. The complexes were active for water oxidation and the redox potentials of the analogues displayed a linear relationship with the Hammet σmeta parameter. It was also found that the complexes form high-valent Ru(VI) species, which are responsible for mediating O–O bond formation.

The last part of the thesis describes the development of a dinuclear ruthenium complex and the catalytic performance for chemical and photochemical water oxidation. It was found that the complex undergoes O–O bond formation via a bridging peroxide intermediate, i.e. an I2M–type mechanism.

Ort, förlag, år, upplaga, sidor
Stockholm: Department of Organic Chemistry, Stockholm University, 2016. s. 67
Nyckelord
homogeneous catalysis, O-O bond formation, photocatalysis, ruthenium, water oxidation
Nationell ämneskategori
Organisk kemi
Forskningsämne
organisk kemi
Identifikatorer
urn:nbn:se:su:diva-134824 (URN)978-91-7649-508-7 (ISBN)978-91-7649-509-4 (ISBN)
Disputation
2016-12-09, Magnéli Hall, Arrhenius Laboratory, Svante Arrhenius väg 16 B, Stockholm, 10:00 (Engelska)
Opponent
Handledare
Tillgänglig från: 2016-11-16 Skapad: 2016-10-19 Senast uppdaterad: 2016-11-04Bibliografiskt granskad

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Laine, Tanja M.Kärkäs, Markus D.Liao, Rong-ZhenÅkermark, TorbjörnLee, Bao-LinKarlsson, Erik A.Siegbahn, Per E. M.Åkermark, Björn
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