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Martin Lutz

Researcher at Utrecht University

Publications -  595
Citations -  18692

Martin Lutz is an academic researcher from Utrecht University. The author has contributed to research in topics: Ligand & Catalysis. The author has an hindex of 62, co-authored 592 publications receiving 17289 citations. Previous affiliations of Martin Lutz include University of Amsterdam & ETH Zurich.

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Electrocatalytic CO2 conversion to oxalate by a copper complex.

TL;DR: A dinuclear Copper(I) complex that is oxidized in air by CO2 rather than O2 is described; the product is a tetranuclear copper(II) complex containing two bridging CO2-derived oxalate groups, which can be nearly quantitatively electrochemically reduced at a relatively accessible potential, regenerating the initial dinuclear copper (I) compound.
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Organoplatinum crystals for gas-triggered switches

TL;DR: The controlled and fully reversible crystalline-state reaction of gaseous SO2 with non-porous crystalline materials consisting of organoplatinum molecules is reported, which modifies the structures of these molecules without affecting their crystallinity.
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Origin of the Bite Angle Effect in Rhodium Diphosphine Catalyzed Hydroformylation.

TL;DR: In this article, the bite angle effect on the rhodium diphosphine catalyzed hydroformylation was investigated in detail, and a series of xantphos-type ligands with natural bite angles ranging from 102° to 121° was synthesized, and the effect of the natural bite angle on coordination chemistry and catalytic performance was studied.
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End-on and side-on peroxo derivatives of non-heme iron complexes with pentadentate ligands: models for putative intermediates in biological iron/dioxygen chemistry.

TL;DR: The synthesis and characterization of a series of iron(II) complexes with pentadentate N5 ligands that react with H( 2)O(2) to generate transient low-spin Fe(III)-OOH intermediates is reported, with first metrical details of the iron-peroxo units in this family of complexes revealed.
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Self-assembled biomimetic [2Fe2S]-hydrogenase-based photocatalyst for molecular hydrogen evolution

TL;DR: In this article, a supramolecular biomimetic approach to form a catalyst that produces molecular hydrogen using light as the energy source is presented, which is composed of an assembly of chromophores to a bis(thiolate)-bridged diiron ([2Fe2S]) based hydrogenase catalyst.