M
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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Journal ArticleDOI
Ni(salen): a System That Forms Many Solvates with Interacting Ni Atoms
Maxime A. Siegler,Martin Lutz +1 more
TL;DR: In this article, the X-ray crystal structure determinations of Ni(salen) and its solvates were carried out based on the determination of the crystal structure of the solvate Ni(Salen)·1.5MeOH at low and room temperature.
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Mechanistic Study on the Ruthenium-Catalyzed Direct Amination of Alcohols
TL;DR: In this paper, the Ru-catalyzed direct amination of alcohols with ammonia was investigated for the RuHCl(CO)(PPh3)3/Xantphos system in order to gain mechanistic insight.
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X-Ray and NMR Study of the Structural Features of SCS-Pincer Metal Complexes of the Group 10 Triad
Cornelis A. Kruithof,H.P. Dijkstra,Martin Lutz,Anthony L. Spek,Robertus J. M. Klein Gebbink,Gerard van Koten +5 more
TL;DR: In this article, the authors characterized 1H and 13C NMR spectroscopy and X-ray crystal structure determination of SCS-pincriminator metal complexes and assigned all dynamic processes (rac/meso isomerization) that occurred in solution.
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Binaphthol‐Based Diphosphite Ligands in Asymmetric Nickel‐Catalyzed Hydrocyanation of Styrene and 1,3‐Cyclohexadiene: Influence of Steric Properties
Jbm Jos Wilting,Mcc Michèle Janssen,Christian Müller,Martin Lutz,Anthony L. Spek,Dieter Vogt +5 more
TL;DR: A series of chiral (R)-binaphthol-based di- phosphite ligands with different substituents was pre-pared and applied in the asymmetric nickel-catalyzed hydrocyanation of styrene and 1,3-cyclohexadiene to investigate the influence of their steric properties.
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Synthesis and Photoluminescence Properties of an Unprecedented Phosphinine–Cu4Br4 Cluster
TL;DR: The molecular structure in the crystal verifies the presence of the heterocubane-type tetrameric cluster [LCuBr]4 (L = 2,4-diphenyl-5-methyl-6-(2,3-dimethylphenyl)phosphinine), which unexpectedly shows in the solid state temperature-independent orange phosphorescence solely from an (3)XMLCT state.