EPR and Quantum Chemical Investigation of a Bioinspired Hydrogenase Model with a Redox-Active Ligand in the First Coordination Sphere
Amélie Kochem, Thomas Weyhermüller, Frank Neese, Maurice van Gastel
Abstract
Amélie Kochem, Thomas Weyhermüller, Frank Neese, Maurice van Gastel
Abstract
Developing biomimetic complexes that model the active site of hydrogenase metalloenzymes in order to catalyze the activation of H 2 is a topic of major interest. Here we report an EPR and computational investigation of a new heteroleptic nickel complex model, with relevance for H 2 production, bearing a P 2 N 2 ligand with proton relay in the second coordination sphere and a redox-active ligand in the first coordination sphere.
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Developing biomimetic complexes that model the active site of hydrogenase metalloenzymes in order to catalyze the activation of H 2 is a topic of major interest. Here we report an EPR and computational investigation of a new heteroleptic nickel complex model, with relevance for H 2 production, bearing a P 2 N 2 ligand with proton relay in the second coordination sphere and a redox-active ligand in the first coordination sphere.
Key concepts: Hydrogenase, Chemistry, Coordination sphere, Ligand (biochemistry), Active site, Electron paramagnetic resonance, Redox, Nickel