Synthesis and Electrocatalysis of Diiron Monothiolate Complexes: Small Molecule Mimics of the [FeFe] Hydrogenase Enzyme
Author:
Affiliation:
1. Department of Chemistry; University of Delhi; Delhi- 110007 India
Publisher
Wiley
Subject
General Chemistry
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/slct.201700084/fullpdf
Reference72 articles.
1. Iron–sulfur protein folds, iron–sulfur chemistry, and evolution
2. Hydrogen generation: Aromatic dithiolate-bridged metal carbonyl complexes as hydrogenase catalytic site models
3. Structural and Functional Analogues of the Active Sites of the [Fe]-, [NiFe]-, and [FeFe]-Hydrogenases
4. Approaches to efficient molecular catalyst systems for photochemical H2 production using [FeFe]-hydrogenase active site mimics
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1. Homogeneous HER electrocatalysis using monothiolate ligand-based {FeS} complexes: a review;Electrochimica Acta;2024-08
2. A new iron(II) complex as bi-functional electrocatalyst for hydrogen evolution reaction and hydrogen peroxide sensing;Journal of Coordination Chemistry;2023-02-16
3. [FeFe] Hydrogenase: 2‐Propanethiolato‐Bridged {FeFe} Systems as Electrocatalysts for Hydrogen Production in Acetonitrile‐Water;European Journal of Inorganic Chemistry;2023-02-13
4. Synthesis, Characterization and Electrochemical Studies of bis(Monothiolato) {FeFe} Complexes [Fe 2 (μ‐SC 6 H 4 ‐OMe‐ m ) 2 (CO) 5 L] (L = CO, PCy 3 , PPh 3 );ChemistrySelect;2022-11-24
5. Spectroscopic and electrochemical comparison of [FeFe]-hydrogenase active-site inspired compounds: Diiron monobenzenethiolate compounds containing electron-donating and withdrawing groups;Polyhedron;2021-03
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