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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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Synthesis, characterisation and crystal structures of new nickel complexes in S4 coordination spheres; an unprecedented rearrangement during ligand synthesis

TL;DR: In this paper, two new nickel(II) complexes were synthesized by in situ deprotection of thiouronium salts in the presence of nickel (II), and they were characterized by analytical, spectroscopic and electrochemical methods.
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Electron Delocalization in Cross‐Conjugated p‐Phenylenevinylidene Oligomers

TL;DR: Electronic spectra and electrochemical data, as well as AM1 and PPP/SCF calculations, reveal that the cross-conjugated compounds basically behave as linearly pi- Conjugated systems in the sense that molecular orbitals are delocalized over the entire structure and systematically change in energy.
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Calcium carbene complexes with boranophosphorano side-arms: CaC[P(Ph)2BH3]2

TL;DR: In both types of complexes delocalization of electron density over the boranoph phosphorano or iminophosphorano substituents does not play a major role.
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Cationic Ruthenium‐Cyclopentadienyl‐Diphosphine Complexes as Catalysts for the Allylation of Phenols with Allyl Alcohol; Relation between Structure and Catalytic Performance in O‐ vs. C‐Allylation

TL;DR: In this paper, a new catalytic method has been investigated to obtain either O- or C-allylated phenolic products using allyl alcohol or diallyl ether as the allyl donor.
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PdII and PtII Complexes of 2-(2′-Pyridyl)-4,6-diphenylphosphinine: Synthesis, Structure, and Reactivity

TL;DR: The coordination chemistry of the bidentate P,N hybrid ligand 2-(2'-pyridyl)-4,6-diphenylphosphinine (1) towards Pd (II) and Pt(II) has been investigated and it is revealed that the reaction with methanol proceeds selectively by syn addition and exclusively to one of the P=C double bonds.