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Optimized spin crossings and transition states for short-range electron transfer in transition metal dimers
Department of Physics, Stockholm University, AlbaNoVa University Center.ORCID iD: 0000-0002-1312-1202
2005 (English)In: Journal of Physical Chemistry B, ISSN 1520-6106, E-ISSN 1520-5207, Vol. 109, no 20, 10513-10520 p.Article in journal (Refereed) Published
Abstract [en]

Electron-transfer reactions in eight mixed-valence manganese dimers are studied using B3LYP. One of the dimers is a model of the active site of manganese catalase, while another represents a basic building block of the oxygen-evolving complex in photosystem II. The adiabatic reactions are characterized by fully optimized transition states where the single imaginary frequency represents the electron-transfer coordinate. When there is antiferromagnetic coupling between different high-spin centers, electron transfer must be accompanied by a spin transition. Spin transitions are characterized by minimum-energy crossing points between spin surfaces. Three reaction mechanisms have been investigated. First, a single-step reaction where spin flip is concerted with electron transfer. Second, an initial transition to a center with intermediate spin that can be followed by electron transfer. Third, an initial transition to a ferromagnetic state from which the electron can be transferred adiabatically. The complexes prefer the third route with rate-determining barriers ranging from 5.7 kcal/mol to 17.2 kcal/mol for different complexes. The origins of these differences are discussed in terms of oxidation states and ligand environments. Many DFT functionals overestimate charge-transfer interactions, but for the present complexes, the error should be limited because of short Mn-Mn distances.

Place, publisher, year, edition, pages
2005. Vol. 109, no 20, 10513-10520 p.
National Category
Natural Sciences
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URN: urn:nbn:se:uu:diva-145470DOI: 10.1021/jp051116qOAI: oai:DiVA.org:uu-145470DiVA: diva2:396510
Available from: 2011-02-10 Created: 2011-02-09 Last updated: 2017-12-11

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Lundberg, Marcus

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