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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NMR Spectroscopic Studies of Palladium(II) Complexes of Bidentate Diphenylphosphane Ligands with Acetate and Tosylate Anions: Complex Formation and Structures
TL;DR: In this article, the synthesis pathway towards Pd-II complexes of functionalized bidentate diphenylphosphane ligands of the type [Pd(ligand)(anion)(2)] and [pd[ligand]-(anion)-2] has been investigated.
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Synthesis of and evidence for electronic communication within heteromultimetallic Tetrakis(NCN-pincer metal) - (Metallo)porphyrin Hybrids
Bart M. J. M. Suijkerbuijk,Duncan M. Tooke,Martin Lutz,Anthony L. Spek,Leonardus W. Jenneskens,Gerard van Koten,Robertus J. M. Klein Gebbink +6 more
TL;DR: Several heteromultimetallic pincer-porphyrin hybrids have been prepared in excellent yields by stepwise metalation of a general precursor, [2H(Br(NCN))(4)], which was designed in such a way so as to guarantee selectivity for either the porphyrin or pincers sites during the metalation steps.
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A Novel CSiP Ring from the Reaction of a Complexed Phosphinidene and a Silene
Mark J. M. Vlaar,Andreas W. Ehlers,Frans J. J. de Kanter,Marius Schakel,Anthony L. Spek,Martin Lutz,Nadejda Sigal,Yitzhak Apeloig,Koop Lammertsma +8 more
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Bis-(thiosemicarbazonato) Zn(II) complexes as building blocks for construction of supramolecular catalysts.
TL;DR: The application of bis-(thiosemicarbazonato) Zn(II) complexes as building blocks in the construction of supramolecular transition metal assemblies is reported and their coordination behaviour towards pyridylphosphine molecules is investigated.
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Generating and Dimerizing the Transient 16-Electron Phosphinidene Complex [Cp*Ir=PAr]: A Theoretical and Experimental Study
Arjan T. Termaten,Tom Nijbacker,Andreas W. Ehlers,Marius Schakel,Martin Lutz,Anthony L. Spek,Michael L. McKee,Koop Lammertsma +7 more
TL;DR: Density functional theory calculations show a preferred bent geometry for the model complex [CpIr=PH], in contrast to the linear structure of [C pIr=NH], which arises because of the large steric congestion in [[Cp*Ir=PAr]2], which forces it toward a more reactive planar structure that is apt to rearrange.