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Six-membered Ring Chelate Complexes of Ru(II): Structural and photophysical effects
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Photochemistry and Molecular Science, Chemical Physics.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Photochemistry and Molecular Science, Chemical Physics.
Uppsala University, Disciplinary Domain of Science and Technology, Chemistry, Department of Photochemistry and Molecular Science, Chemical Physics.
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2007 (English)In: Inorganic Chemistry, ISSN 0020-1669, E-ISSN 1520-510X, Vol. 46, no 24, 10354-10364 p.Article in journal (Refereed) Published
Abstract [en]

The structural and photophysical properties of Ru(II)−polypyridyl complexes with five- and six-membered chelate rings were studied for two bis-tridentate and two tris-bidentate complexes. The photophysical effect of introducing a six-membered chelate ring is most pronounced for the tridentate complex, leading to a room-temperature excited-state lifetime of 810 ns, a substantial increase from 180 ns for the five-membered chelate ring model complex. Contrasting this, the effect is the opposite in tris-bidentate complexes, in which the lifetime decreases from 430 ns to around 1 ns in going from a five-membered to six-membered chelate ring. All of the complexes were studied spectroscopically at both 80 K and ambient temperatures, and the temperature dependence of the excited-state lifetime was investigated for both of the bis-tridentate complexes. The main reason for the long excited-state lifetime in the six-membered chelate ring bis-tridentate complex was found to be a strong retardation of the activated decay via metal-centered states, largely due to an increased ligand field splitting due to the complex having a more-octahedral geometry.

Place, publisher, year, edition, pages
2007. Vol. 46, no 24, 10354-10364 p.
National Category
Chemical Sciences
Identifiers
URN: urn:nbn:se:uu:diva-95086DOI: 10.1021/ic7011827ISI: 000251109500039PubMedID: 17975915OAI: oai:DiVA.org:uu-95086DiVA: diva2:169162
Available from: 2006-11-09 Created: 2006-11-09 Last updated: 2017-12-14Bibliographically approved
In thesis
1. Tuning of the Excited State Properties of Ruthenium(II)-Polypyridyl Complexes
Open this publication in new window or tab >>Tuning of the Excited State Properties of Ruthenium(II)-Polypyridyl Complexes
2006 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Processes where a molecule absorbs visible light and then converts the solar energy into chemical energy are important in many biological systems, such as photosynthesis and also in many technical applications e.g. photovoltaics. This thesis describes a part of a multidisciplinary project, aiming at a functional mimic of the natural photosynthesis, with the overall goal of production of a renewable fuel from sun and water. More specific, the thesis is focused on design and photophysical characterization of new photosensitizers, i.e. light absorbers that should be capable of transferring electrons to an acceptor and be suitable building blocks for supramolecular rod-like donor-photosensitizer-acceptor arrays.

The excited state lifetime, the excited state energy and the geometry are important properties for a photosensitizer. The work presented here describes a new strategy to obtain longer excited state lifetimes of the geometrically favorable Ru(II)-bistridentate type complexes, without a concomitant substantial decrease in excited state energy. The basic idea is that a more octahedral coordination around the Ru will lead to longer excited state lifetimes. In the first generation of new photosensitizers a 50-fold increase of the excited state lifetime was observed, going from 0.25 ns for the model complex to 15 ns for the best photosensitizer. The second generation goes another step forward, to an excited state lifetime of 810 ns. Furthermore, the third generation of new photosensitizers show excited state lifetimes in the 0.45 - 5.5 microsecond region at room temperature, a significant improvement. In addition, the third generation of photosensitizers are suitable for further symmetric attachment of electron donor and acceptor motifs, and it is shown that the favorable properties are maintained upon the attachment of anchoring groups. The reactivity of the excited state towards light-induced reactions is proved and the photostability is sufficient so the new design strategy has proven successful.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis, 2006. 79 p.
Series
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 237
Keyword
Physical chemistry, Artificial photosynthesis, Ruthenium(II), Bistridentate complexes, Excited state lifetime, Linear donor-photosenstizer-acceptor arrays, Temperature dependence, Excited state decay, Fysikalisk kemi
Identifiers
urn:nbn:se:uu:diva-7230 (URN)91-554-6707-5 (ISBN)
Public defence
2006-12-01, Häggsalen, Ångströmlaboratoriet, Lägerhyddsvägen 1, Uppsala, 09:30
Opponent
Supervisors
Available from: 2006-11-09 Created: 2006-11-09 Last updated: 2011-06-10Bibliographically approved

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Becker, Hans-ChristianHammarström, Leif

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