M
Mark R. Ringenberg
Researcher at University of Stuttgart
Publications - 63
Citations - 1299
Mark R. Ringenberg is an academic researcher from University of Stuttgart. The author has contributed to research in topics: Chemistry & Catalysis. The author has an hindex of 13, co-authored 48 publications receiving 1096 citations. Previous affiliations of Mark R. Ringenberg include University of Illinois at Urbana–Champaign & University of Basel.
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Redox-active ligands in catalysis.
TL;DR: This work has shown that using redox-active moieties in the vicinity of metal centers to catalyze challenging transformations enables chemists to impart noble-metal character to less toxic, and cost effective 3d transitional metals, such as Fe or Cu, in multi-electron catalytic reactions.
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Redox-switched oxidation of dihydrogen using a non-innocent ligand.
TL;DR: The catalytic oxidation of H2 was established by electrochemical methods to be associated with the monocation and salts of [1]+, which were characterized by crystallographically, EPR, and elemental analyses.
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Artificial metalloenzymes for olefin metathesis based on the biotin-(strept)avidin technology
TL;DR: Incorporation of a biotinylated Hoveyda-Grubbs catalyst within (strept)avidin affords artificial metalloenzymes for the ring-closing metathesis of N-tosyl diallylamine in aqueous solution.
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Merging the Best of Two Worlds : Artificial Metalloenzymes for Enantioselective Catalysis
TL;DR: The recent progress is summarized and the challenges ahead are outlined in artificial metalloenzymes, which combine attractive features of both homogeneous and enzymatic systems.
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Heteroleptic Copper Photosensitizers: Why an Extended π-System Does Not Automatically Lead to Enhanced Hydrogen Production.
Martin Heberle,Stefanie Tschierlei,Stefanie Tschierlei,Nils Rockstroh,Mark R. Ringenberg,Wolfgang Frey,Henrik Junge,Matthias Beller,Stefan Lochbrunner,Michael Karnahl +9 more
TL;DR: In this article, a series of heteroleptic copper(I) photosensitizers with an extended π-system in the backbone of the diimine ligand has been prepared.