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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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Induction of Chirotopicity in the Self-Assembly Process of Heterocuprates: Structural and Stereochemical Aspects of Neutral CuLi2BrAryl2 Aggregates

TL;DR: In this paper, self-assembling reactions of the ortho-diamine chelated aryllithium dimers with 1 equiv of CuBr resulted in the selective formation of hetero cuprates 1, 2, 3a, and 3b, respectively.
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Reactivity of a Ruthenium-Carbonyl Complex in the Methanol Dehydrogenation Reaction.

TL;DR: The ruthenium complex Ru(sal binapht)(CO)(Pi‐Pr3) {salbinapht=2‐[({2‐hydroxybenzyl)amino]‐[1,1′‐binaphthalen]‐2‐yl}imino)methyl]phenolato} catalyzes the methanol dehydrogenation reaction in the presence of base and water to yield H2, formate, and carbonate.
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Introduction of Bulky Substituents at the Bridgehead Position of a 9-Silatriptycene: Pentacoordinate Hydridoorganylsilicates as Intermediates

TL;DR: The reaction of 10-phenyl-10-germa-9-silatriptycene (1b) with phenyllithium in THF/HMPA produced 9,10-diphenyl- 10-germma- 9-silatio-nictycenes (1a), which had hitherto not been accessible as discussed by the authors.
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CuI Thiolate Reactivity with Dioxygen: The Formation of CuII Sulfinate and CuII Sulfonate Species via a CuII Thiolate Intermediate

TL;DR: Monitoring the oxidation of 1 by UV-vis indicates that the oxidation proceeds via a dinuclear Cu(II) μ-thiolate complex, providing a model for the oxidative degeneration of copper-sulfur enzymes.
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Reductive Elimination at an Ortho-Metalated Iridium(III) Hydride Bearing a Tripodal Tetraphosphorus Ligand

TL;DR: In this paper, the synthesis of a tetradentate C3-symmetric tripodal, tetradate ligand with only phosphorus atoms as donor groups was described, starting from commercially available o-tolyldiphenylphosphine, and its molecular structure was determined by X-ray crystallographic analysis.