J
Joost N. H. Reek
Researcher at University of Amsterdam
Publications - 488
Citations - 23869
Joost N. H. Reek is an academic researcher from University of Amsterdam. The author has contributed to research in topics: Catalysis & Hydroformylation. The author has an hindex of 74, co-authored 458 publications receiving 21217 citations. Previous affiliations of Joost N. H. Reek include Wageningen University and Research Centre & Virginia Tech.
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Journal ArticleDOI
Early stages of catalyst aging in the iridium mediated water oxidation reaction
Dennis G. H. Hetterscheid,Cornelis J. M. van der Ham,Oscar Diaz-Morales,Martinus W. G. M. Verhoeven,Alessandro Longo,Dipanjan Banerjee,J.W. Niemantsverdriet,Joost N. H. Reek,Martin C. Feiters +8 more
TL;DR: XPS and XAS studies reveal that the species present at the electrode interface is best described as a partly oxidized molecular species rather than the formation of large aggregates of iridium oxide, in line with the unique kinetic profile of the parent complex in the water oxidation reaction.
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Intermolecular C-H activation with an Ir-METAMORPhos piano-stool complex--multiple reaction steps at a reactive ligand.
TL;DR: A stoichiometric anti-Markovnikov C-N bond formation involving ligand reactivity in multiple steps along the reaction coordinate is described, which affords a highly unusual four-membered iridacycle bearing an exo-cyclic C=C double bond.
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Organocatalysis in Confined Spaces
TL;DR: In this paper, the authors considered a powerful strategy for achieving unique transformations in a very efficient way by encapsulation of the catalytic active site in an analogous manner as enzymes, which can often give rise to unprecedented selectivities.
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Anode Preparation Strategies for the Electrocatalytic Oxidation of Water Based on Strong Interactions between Multiwalled Carbon Nanotubes and Cationic Acetylammonium Pyrene Moieties in Aqueous Solutions
TL;DR: The immobilization strategy is limited to applications below 1.4 V vs normal hydrogen electrode (NHE) as oxidation of the pyrene backbone is evident at higher potentials.
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Halogenated earth abundant metalloporphyrins as photostable sensitizers for visible-light-driven water oxidation in a neutral phosphate buffer solution
TL;DR: The molecular system based on earth-abundant (first-row transition) metals in concentrated phosphate buffer solution successfully demonstrate long-term visible-light-driven water oxidation and the solar photon capturing abilities of halogenated metalloporphyrins are comparable to that of the natural photosynthetic pigment, chlorophyll a.