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Electron paramagnetic resonance study of the S=1/2 ground state of a radiolysis-generated manganese(III)-trimanganese(IV) form of [Mn-IV;O-4(6)(bipy)(6)](4+) (bipy=2,2'-bipyridine). Comparison with the photosynthetic Oxygen Evolving Complex

Författare

  • Geneviève Blondin
  • Roman Davydov
  • Christian Philouze
  • Marie-France Charlot
  • Stenbjörn Styring
  • Björn Åkermark
  • Jean-Jacques Girerd
  • Alain Boussac

Summary, in English

gamma-Ray irradiation at liquid nitrogen temperature of a dimethylformamide solution of the tetranuclear complex [(Mn4O6)-O-IV(bipy)(6)](4+) (bipy = 2,2'-bipyridine) allowed the generation of the first mixed-valence tetranuclear system containing Mn-III and Mn-IV ions and exhibiting a S = 1/2 ground state. The X-band EPR spectrum of this tetranuclear system has been obtained. Simulations have been undertaken and the Mn hyperfine coupling tensors determined clearly show a (MnMn3IV)-Mn-III, composition for the EPR active species. A general approach for the analysis of the isotropic components of the Mn hyperfine tensors is presented in detail. This allowed the determination of the spin projection value for each Mn site. A three J coupling scheme assuming that the linear topology of the starting compound remains is able to reproduce these spin projection values if and only if the Mn-III ion is located at a terminal position in a N4O2 environment. The EPR signal of this [Mn4O6(bipy)(6)](3+) species is compared with the multiline signal observed in the S-2 state of the photosynthetic Oxygen Evolving Complex.

Publiceringsår

1997

Språk

Engelska

Sidor

4069-4074

Publikation/Tidskrift/Serie

Journal of the Chemical Society. Dalton Transactions

Volym

1997

Issue

21

Dokumenttyp

Artikel i tidskrift

Förlag

Royal Society of Chemistry

Ämne

  • Biological Sciences

Nyckelord

  • PLANTS
  • WATER
  • S2 STATE
  • SIMULATION
  • REDOX PROPERTIES
  • MANGANESE CLUSTER
  • MULTILINE EPR SIGNALS
  • MN-OXO CLUSTER
  • PHOTOSYSTEM-II
  • OXIDATION

Status

Published

ISBN/ISSN/Övrigt

  • ISSN: 1472-7773