about
Direct Observation of an Iron-Bound Terminal Hydride in [FeFe]-Hydrogenase by Nuclear Resonance Vibrational Spectroscopy.Reaction Coordinate Leading to H2 Production in [FeFe]-Hydrogenase Identified by Nuclear Resonance Vibrational Spectroscopy and Density Functional Theory.Sterically Stabilized Terminal Hydride of a Diiron Dithiolate.Electron-Rich, Diiron Bis(monothiolato) Carbonyls: C-S Bond Homolysis in a Mixed Valence Diiron Dithiolate.A [RuRu] Analogue of an [FeFe]-Hydrogenase Traps the Key Hydride Intermediate of the Catalytic CycleThe binuclear cluster of [FeFe] hydrogenase is formed with sulfur donated by cysteine of an [Fe(Cys)(CO)2(CN)] organometallic precursorAsymmetry in the Ligand Coordination Sphere of the [FeFe] Hydrogenase Active Site Is Reflected in the Magnetic Spin Interactions of the Aza-propanedithiolate LigandSynthetic Designs and Structural Investigations of Biomimetic Ni-Fe ThiolatesRedox and "Antioxidant" Properties of Fe2(μ-SH)2(CO)4(PPh3)2Spectroscopic and Computational Evidence that [FeFe] Hydrogenases Operate Exclusively with CO-Bridged IntermediatesIron Carbide-Sulfide Carbonyl Clusters
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P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Thomas B Rauchfuss
@en
Thomas B Rauchfuss
@nl
type
label
Thomas B Rauchfuss
@en
Thomas B Rauchfuss
@nl
prefLabel
Thomas B Rauchfuss
@en
Thomas B Rauchfuss
@nl
P31
P496
0000-0003-2547-5128