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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Synthesis, Crystal Structure, and Redox and Photophysical Properties of Novel Bisphosphinoaryl RuII-Terpyridine Complexes
Marcella Gagliardo,Harm P. Dijkstra,Paolo Coppo,Luisa De Cola,Martin Lutz,Anthony L. Spek,Gerard P. M. van Klink,Gerard van Koten +7 more
TL;DR: In this paper, the structure of the [Ru(PCP)(tpy)]Cl complexes was determined by X-ray crystallography and the spectroscopic and electrochemical properties of these complexes were compared with those obtained for [Ru{C 6 H 3 (CH 2 NMe 2 ) 2 -2,6}(tpy](Cl) (3) containing the monoanionic bisaminoaryl ligand (NCN).
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A novel ruthenium carbene dimer that is active in the metathesis of internal alkenes; the crystal structure of Ru2(CHPh)2(CF3CO2)2(μ-CF3CO2)2(PCy3)2(μ-H2O)
TL;DR: The reaction of Ru(CHPh)Cl 2 (PCy 3 ) 2 ( 1 ) with two equivalents of CF 3 CO 2 Ag gives Ru 2 ( CHPh) 2 (CF 3 CO2 ) 2(μ-CF 3 Co 2 ) 2PCy3 ) 2μ-H 2 O) ( 2 ) in high yield.
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Reaction Progress Kinetic Analysis as a Tool To Reveal Ligand Effects in Ce(IV)-Driven IrCp*-Catalyzed Water Oxidation
TL;DR: A series of iridium-based complexes evaluated in Ce(IV)-driven water oxidation catalysis found that some bidentate ligands result in relatively slow catalysis, and the first-order in iridium supports the presence of mononuclear active species; however, other bidentates form the more active dinuclear species.
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Synthesis and characterization of Pd(II)-methyl complexes with N-heterocyclic carbene-amine ligands.
Stefan Warsink,Sandra Y. de Boer,Lianne M. Jongens,Ching-Feng Fu,Shiuh-Tzung Liu,Jwu-Ting Chen,Martin Lutz,Anthony L. Spek,Cornelis J. Elsevier +8 more
TL;DR: The neutral and cationic cis-methyl-palladium(NHC) complexes are not prone to reductive elimination, which is normally a major degenerative pathway for this type of complex, and under carbon monoxide atmosphere rapid reductive Elimination of the acyl-imidazolium salt was observed.
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Facile Access to Key Reactive Intermediates in the Pd/PR3‐Catalyzed Telomerization of 1,3‐Butadiene
Peter J. C. Hausoul,Andrei N. Parvulescu,Martin Lutz,Anthony L. Spek,Pieter C. A. Bruijnincx,Bert M. Weckhuysen,Robertus J. M. Klein Gebbink +6 more
TL;DR: The Pd-catalyzed telomerization of 1,3-dienes is an important atom-efficient transformation, which effectively adds nucleophiles over two C C coupled dienes in a 1,6- or 3, 6-fashion and provides an economically attractive route for the production of C8 bulk chemicals.