Self-assembled biomimetic [2Fe2S]-hydrogenase-based photocatalyst for molecular hydrogen evolution
- 30 June 2009
- journal article
- Published by Proceedings of the National Academy of Sciences in Proceedings of the National Academy of Sciences
- Vol. 106 (26), 10460-10465
- https://doi.org/10.1073/pnas.0809666106
Abstract
The large-scale production of clean energy is one of the major challenges society is currently facing. Molecular hydrogen is envisaged as a key green fuel for the future, but it becomes a sustainable alternative for classical fuels only if it is also produced in a clean fashion. Here, we report a supramolecular biomimetic approach to form a catalyst that produces molecular hydrogen using light as the energy source. It is composed of an assembly of chromophores to a bis(thiolate)-bridged diiron ([2Fe2S]) based hydrogenase catalyst. The supramolecular building block approach introduced in this article enabled the easy formation of a series of complexes, which are all thoroughly characterized, revealing that the photoactivity of the catalyst assembly strongly depends on its nature. The active species, formed from different complexes, appears to be the [Fe(2)(micro-pdt)(CO)(4){PPh(2)(4-py)}(2)] (3) with 2 different types of porphyrins (5a and 5b) coordinated to it. The modular supramolecular approach was important in this study as with a limited number of building blocks several different complexes were generated.Keywords
This publication has 30 references indexed in Scilit:
- Models for the Hydrogenases Put the Focus Where It Should Be—HydrogenAngewandte Chemie International Edition, 2007
- Fe–S complexes containing five-membered heterocycles: novel models for the active site of hydrogenases with unusual low reduction potentialDalton Transactions, 2007
- Powering the planet: Chemical challenges in solar energy utilizationProceedings of the National Academy of Sciences, 2006
- Assignment of Molecular Structures to the Electrochemical Reduction Products of Diiron Compounds Related to [Fe−Fe] Hydrogenase: A Combined Experimental and Density Functional Theory StudyInorganic Chemistry, 2006
- Bidentate ligands by supramolecular chemistry—the future for catalysis?Dalton Transactions, 2006
- De Novo Design of Synthetic Di-Iron(I) Complexes as Structural Models of the Reduced Form of Iron−Iron HydrogenaseInorganic Chemistry, 2006
- What Can Replace Cheap Oil--and When?Science, 2005
- Influence of Tertiary Phosphanes on the Coordination Configurations and Electrochemical Properties of Iron Hydrogenase Model Complexes: Crystal Structures of [(μ‐S2C3H6)Fe2(CO)6–nLn] (L = PMe2Ph, n = 1, 2; PPh3, P(OEt)3, n = 1)European Journal of Inorganic Chemistry, 2005
- Supraphos: A Supramolecular Strategy To Prepare Bidentate LigandsJournal of the American Chemical Society, 2004
- Synthesis and properties of iron-group hydrido-cyano complexes trans-[MH(CN)(L)2], M = Fe, Ru or Os, L = diphosphine, and their hydrogen, trifluoroboron and triphenylboron isocyanide derivatives of the type trans-[MH(CNH)(L)2]O3SCF3, trans-[MH(CNBX3)(L)2], X = F or Ph, and trans-[M(H2)(CNBF3)(dppp)2]BF4 [dppp = Ph2P(CH2)3PPh2]J. Chem. Soc., Dalton Trans., 2000