Abstract
A phosphoramidite modified [FeFe]H2ase mimic is studied as a model for photodriven production of H2. On cathodic activation, the pyridyl-phosphoramidite complex exhibits a strongly enhanced rate of proton reduction over the previously reported pyridylphosphine model at the same overpotential. Analysis of the cyclic voltammograms shows an apparent H 2 evolution rate strongly influenced by the presence of both side-bound pyridyl and phosphorous-bound dimethylamino moieties at the phosphoramidite ligands. This difference is ascribed to the basic amines acting as proton relays. © the Partner Organisations 2014.
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CITATION STYLE
Derossi, S., Becker, R., Li, P., Hartl, F., & Reek, J. N. H. (2014). A phosphoramidite-based [FeFe]H2ase functional mimic displaying fast electrocatalytic proton reduction. Dalton Transactions, 43(22), 8363–8367. https://doi.org/10.1039/c3dt53471e
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