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Literature summary for 1.12.99.6 extracted from

  • Justice, A.K.; De Gioia, L.; Nilges, M.J.; Rauchfuss, T.B.; Wilson, S.R.; Zampella, G.
    Redox and structural properties of mixed-valence models for the active site of the [FeFe]-hydrogenase: progress and challenges (2008), Inorg. Chem., 47, 7405-7414.
    View publication on PubMedView publication on EuropePMC

Metals/Ions

Metals/Ions Comment Organism Structure
Fe the Fe(CO)2(Pi-Pr3) site is rotated in solution, driven by steric factors. Fe atom featuring a vacant apical coordination position is an electrophilic Fe(I) center. One-electron oxidation of [Fe2(S2C2H4)(CN)(CO)3(dppv)]- results in 2e oxidation of 0.5 equiv to give the micro-cyano derivative [FeI2(S2C2H4)(CO)3(dppv)](micro-CN)[FeII2(S2C2H4)(micro-CO)(CO)2(CN)(dppv)] synthetic construct

Organism

Organism UniProt Comment Textmining
synthetic construct
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-
-

Synonyms

Synonyms Comment Organism
[FeFe]-hydrogenase
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synthetic construct