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[NiFe], [FeFe], and [Fe] hydrogenase models from isomers.

Seiji OgoTakahiro KishimaTakeshi YatabeKeishi MiyazawaRyunosuke YamasakiTakahiro MatsumotoTatsuya AndoMitsuhiro KikkawaMiho IsegawaKi-Seok YoonShinya Hayami
Published in: Science advances (2020)
The study of hydrogenase enzymes (H2ases) is necessary because of their importance to a future hydrogen energy economy. These enzymes come in three distinct classes: [NiFe] H2ases, which have a propensity toward H2 oxidation; [FeFe] H2ases, which have a propensity toward H2 evolution; and [Fe] H2ases, which catalyze H- transfer. Modeling these enzymes has so far treated them as different species, which is understandable given the different cores and ligand sets of the natural molecules. Here, we demonstrate, using x-ray analysis and nuclear magnetic resonance, infrared, Mössbauer spectroscopies, and electrochemical measurement, that the catalytic properties of all three enzymes can be mimicked with only three isomers of the same NiFe complex.
Keyphrases
  • magnetic resonance
  • gold nanoparticles
  • visible light
  • hydrogen peroxide
  • computed tomography
  • current status
  • ionic liquid
  • molecularly imprinted
  • dual energy
  • data analysis
  • solid phase extraction