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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End Groups of Functionalized Siloxane Oligomers Direct Block-Copolymeric or Liquid-Crystalline Self-Assembly Behavior.
TL;DR: The importance of end groups in high χ-low N block molecules is shown, where block-copolymer-like self-assembly in the authors' UPy-functionalized oligodimethylsiloxanes relies upon the dominance of phase separation effects over directional end group aggregation.
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Base-free production of H2 by dehydrogenation of formic acid using an iridium-bisMETAMORPhos complex.
Sander Oldenhof,Bas de Bruin,Martin Lutz,Maxime A. Siegler,Frederic W. Patureau,Frederic W. Patureau,Jarl Ivar van der Vlugt,Joost N. H. Reek +7 more
TL;DR: An iridium complex based on a cooperative ligand that functions as an internal base is reported that can rapidly and cleanly dehydrogenate formic acid in absence of external base.
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Iron(II) complexes with bio-inspired N,N,O ligands as oxidation catalysts: olefin epoxidation and cis-dihydroxylation.
Pieter C. A. Bruijnincx,Inge L. C. Buurmans,Silvia Gosiewska,Marcel A. H. Moelands,Martin Lutz,Anthony L. Spek,Gerard van Koten,Robertus J. M. Klein Gebbink +7 more
TL;DR: The iron(II) coordination chemistry of the ligands 3,3-bis(1-methylimidazol-2-yl)propionate (L1) and its neutral propyl ester analogue propyl 3, 3-bis (1- methylimodazol -2-YL)propIONate (PrL1), thought to be similar to those of the Rieske oxygenases, is reported.
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Multinuclear Magnesium Hydride Clusters: Selective Reduction and Catalytic Hydroboration of Pyridines
TL;DR: In this article, an extended network of C−H···C πinteractions and π-stacking interactions is found. But the regioselectivity of the stochastic reaction is not known.
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Encapsulated transition metal catalysts comprising peripheral Zn(II)salen building blocks: template-controlled reactivity and selectivity in hydroformylation catalysis
TL;DR: Encapsulated phosphane ligands can be easily constructed through coordinative interactions between Zn(II)-salphen complexes and pyridylphosphane templates; the template has a pronounced impact on the catalyst structure and consequently on the performance in the hydroformylation of 1-octene.