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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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Lutidine-derived Ru-CNC hydrogenation pincer catalysts with versatile coordination properties

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

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

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

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.