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Issue 8, 2011
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Proton management as a design principle for hydrogenase-inspired catalysts

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Abstract

The properties of the hydrogenase-inspired [Ni(PNP)2]2+ (PNP = Et2PCH2NMeCH2PEt2) catalyst for homogeneous hydrogen oxidation in acetonitrile solution are explored from a theoretical perspective for hydrogen production. The defining characteristic of this catalyst is the presence of pendent bases in the second coordination sphere that function as proton relays between the solution and the metal center. DFT calculations of the possible intermediates along proposed catalytic pathways are carried out and used to construct coupled Pourbaix diagrams of the redox processes and free-energy profiles along the reaction pathways. Analysis of the coupled Pourbaix diagrams reveals insights into the intermediate species and the mechanisms favored at different pH values of the solution. Consideration of the acid–base behavior of the metal hydride and H2 adduct species imposes additional constraints on the reaction mechanism, which can involve intramolecular as well as intermolecular proton-coupled electron-transfer steps. The efficacy of the catalyst is shown to depend critically on the pKa values of these potential intermediates, as they control both the species in solution at a given pH and the free-energy profile of reaction pathways. Optimal relationships among these pKa values can be identified, and it is demonstrated that “proton management”, i.e., the manipulation of these pKa values (e.g., through choice of metal or substituents on ligands), can serve as a design principle for improved catalytic behavior.

Graphical abstract: Proton management as a design principle for hydrogenase-inspired catalysts

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Publication details

The article was received on 15 Feb 2011, accepted on 03 May 2011 and first published on 23 Jun 2011


Article type: Paper
DOI: 10.1039/C1EE01170G
Citation: Energy Environ. Sci., 2011,4, 3008-3020
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    Proton management as a design principle for hydrogenase-inspired catalysts

    Y. A. Small, D. L. DuBois, E. Fujita and J. T. Muckerman, Energy Environ. Sci., 2011, 4, 3008
    DOI: 10.1039/C1EE01170G

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