Mixed Valence (μ‐Phenoxido) Fe II Fe III and Fe III Fe IV Compounds: Electron and Proton Transfers
Autor: | Patrick Dubourdeaux, Geneviève Blondin, Jean-Marc Latour |
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Přispěvatelé: | Physiochimie des Métaux (PMB), Laboratoire de Chimie et Biologie des Métaux (LCBM - UMR 5249), Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche Interdisciplinaire de Grenoble (IRIG), Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Direction de Recherche Fondamentale (CEA) (DRF (CEA)), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Grenoble Alpes (UGA)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Institut de Recherche Interdisciplinaire de Grenoble (IRIG), Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)-Université Grenoble Alpes (UGA) |
Rok vydání: | 2021 |
Předmět: |
Valence (chemistry)
proton transfer biology Proton Chemistry Active site Intervalence charge transfer electron transfer Photochemistry Redox Tautomer Atomic and Molecular Physics and Optics Ion tautomerism Electron transfer CPET biology.protein [CHIM.COOR]Chemical Sciences/Coordination chemistry Physical and Theoretical Chemistry mixed-valent diiron compound |
Zdroj: | ChemPhysChem ChemPhysChem, 2022, 23 (2), pp.e202100399. ⟨10.1002/cphc.202100399⟩ |
ISSN: | 1439-7641 1439-4235 |
DOI: | 10.1002/cphc.202100399 |
Popis: | International audience; Mixed-valence non-heme diiron centers are present at the active sites of a few enzymes and confer them interesting reactivities with the two ions acting in concert. Related (μ-phenoxido)diiron complexes have been developed as enzyme mimics. They exhibit very rich spectroscopic properties enabling independent monitoring of each individual ion, which proved useful for mechanistic studies of catalytic hydrolysis and oxidation reactions. In our studies of such complexes, we observed that these compounds give rise to a wide variety of electron transfers (intervalence charge transfer), proton transfers (tautomerism), coupled electron and proton transfers (H. abstraction and PCET). In this minireview, we present and analyze the main results illustrating the latter aspects. |
Databáze: | OpenAIRE |
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