Mimicking the electron donor side of Photosystem II in artificial photosynthesis.

Abstract:

:This review focuses on our recent efforts in synthetic ruthenium-tyrosine-manganese chemistry mimicking the donor side reactions of Photosystem II. Tyrosine and tryptophan residues were linked to ruthenium photosensitizers, which resulted in model complexes for proton-coupled electron transfer from amino acids. A new mechanistic model was proposed and used to design complexes in which the mechanism could be switched between concerted and step-wise proton-coupled electron transfer. Moreover, a manganese dimer linked to a ruthenium complex could be oxidized in three successive steps, from Mn (2) (II,II) to Mn (2) (III,IV) by the photo-oxidized ruthenium sensitizer. This was possible thanks to a charge compensating ligand exchange in the manganese complex. Detailed studies of the ligand exchange suggested that at high water concentrations, each oxidation step is coupled to a proton-release of water-derived ligands, analogous to the oxidation steps of the manganese cluster of Photosystem II.

journal_name

Photosynth Res

journal_title

Photosynthesis research

authors

Lomoth R,Magnuson A,Sjödin M,Huang P,Styring S,Hammarström L

doi

10.1007/s11120-005-9005-0

subject

Has Abstract

pub_date

2006-01-01 00:00:00

pages

25-40

issue

1

eissn

0166-8595

issn

1573-5079

journal_volume

87

pub_type

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