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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Lutidine-derived Ru-CNC hydrogenation pincer catalysts with versatile coordination properties
Georgy A. Filonenko,Elena Cosimi,Laurent Lefort,Matthew P. Conley,Christophe Copéret,Martin Lutz,Emiel J. M. Hensen,Evgeny A. Pidko +7 more
TL;DR: In this article, a bis-N-heterocyclic carbene (NHC) ruthenium CNC-pincer complexes (Ru-CNCs) were prepared.
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Bifunctional Pincer-type Organometallics as Substrates for Organic Transformations and as Novel Building Blocks for Polymetallic Materials
Gema Rodríguez,Martin Albrecht,Jeroen Schoenmaker,Alan Ford,Martin Lutz,Anthony L. Spek,Gerard van Koten +6 more
TL;DR: The reactivity of the bifunctionalized ligand NC(Br)N-I 1 has been studied as a versatile synthon for organic and/or organometallic synthesis, revealing the remarkable stability of their M-C sigma-bond and opening an easy route for the synthesis of mono- and (hetero)bimetallic building blocks.
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The formazanate ligand as an electron reservoir : Bis(formazanate) zinc complexes isolated in three redox states
TL;DR: The synthesis of bis(formazanate) zinc complexes is described, which have well-behaved redox-chemistry, with the ligands functioning as a reversible electron reservoir and the stability of these ligand-based radicals is a result of the delocalization of the unpaired electron over four nitrogen atoms in the ligand backbone.
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Modeling the 2-His-1-Carboxylate Facial Triad: Iron−Catecholato Complexes as Structural and Functional Models of the Extradiol Cleaving Dioxygenases
Pieter C. A. Bruijnincx,Martin Lutz,Anthony L. Spek,Wilfred R. Hagen,Bert M. Weckhuysen,Gerard van Koten,Robertus J. M. Klein Gebbink +6 more
TL;DR: The mononuclear iron(III)-tetrachlorocatecholato complex was determined by single-crystal X-ray diffraction, which shows a facial N,N,O capping mode of the ligand, which is a new example to the small group of synthetic iron complexes capable of eliciting extradiol-type cleavage and provide more insight into the factors determining the regioselectivity of the enzymes.
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Supramolecular zinc(II)salphen motifs: Reversible dimerization and templated dimeric structures
Arjan W. Kleij,Mark Kuil,Martin Lutz,Duncan M. Tooke,Anthony L. Spek,Paul C. J. Kamer,Piet W. N. M. van Leeuwen,Joost N. H. Reek +7 more
TL;DR: In this article, the formation of a dimeric structure of a nonsymmetric Zn(II)salphen complex is reported and the X-ray molecular structure shows the formation an oxygen-bridged species.