Prof. Dr. Roger Alberto - A Special Collection of articles honouring an outstanding scientist, collaborator, and friend.
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http://dx.doi.org/10.1002/chem.202404631 | DOI Listing |
Dalton Trans
December 2024
Bioactive Compounds Development Research Group, Federal University of Triângulo Mineiro, Av. Dr. Ran-dolfo Borges 1400, Uberaba 38025-440, MG, Brazil.
The diagnosis and treatment of Chagas disease (CD) in the chronic phase remains a challenge. With that in mind, a potential theranostic device based on the trypanocidal agent known as megazol and the -M(CO) (M = Re or Tc) fragment is proposed in the present work. The peripheral structure of megazol (L) was modified to obtain the compounds L (R1 = H, R2 = Me and R1 = R2 = Me), which were used in the syntheses of complexes of composition [ReBr(CO)L].
View Article and Find Full Text PDFInorg Chem
September 2024
University of Zurich, Department of Chemistry, Winterthurerstrasse 190, 8057 Zürich, Switzerland.
We report the synthesis, characterization, and in vitro biological activities of [Re(η-arene)]-terpyridine conjugates and their Cu complexes. The terpyridine (terpy) chelators were attached to the [Re(η-arene)] scaffold via secondary amine linkers allowing for heteroleptic mono- and homoleptic bis-terpyridine-substituted chelators. Complexation with CuCl afforded the respective square pyramidal [Cu(terpy)Cl] complexes hosted on the [Re(η-arene)] scaffold.
View Article and Find Full Text PDFACS Energy Lett
August 2024
Department of Chemistry, University of Zurich, Zurich, 8057, Switzerland.
Molybdenum sulfide serves as an effective nonprecious metal catalyst for hydrogen evolution, primarily active at edge sites with unsaturated molybdenum sites or terminal disulfides. To improve the activity at a low loading density, two molybdenum sulfide clusters, [MoS] and [MoS], were investigated. The MoS molecular catalysts were heterogenized on SbSe with a simple soaking treatment, resulting in a thin catalyst layer of only a few nanometers that gave up to 20 mA cm under one sun illumination.
View Article and Find Full Text PDFChemistry
August 2024
Department of Chemistry, University of Zurich, Winterthurerstrasse 190, Switzerland.
Inorg Chem
February 2024
Department of Chemistry, University of Zurich, Winterthurerstrasse 190, Zurich 8057, Switzerland.
Here, we present the light-driven reactions of [Re(η-CH)(η-CH)] () with nitriles, phosphines, and isocyanides, which are added to via a ring slippage of the tropylium cation from η to η, forming [Re(η-CH)(η-CH)(L)] (L= acetonitrile ; 2-phenylacetonitrile ; 1,3,5-triaza-5-phosphoadamantane (PTA) ; -butyl isocyanide ; benzyl isocyanide ) and [Re(η-CH)(η-CH)(L)] with L = (ethane-1,2-diyl)bis(diphenylphosphane) (dppe) . To compare the reactivities of rhenium and technetium, we also investigated the synthesis of [Tc(η-CH)], its substitution of naphthalene with cyclohepta-1,3,5-triene to obtain [Tc(η-CH)(η-CH)], and its reactivity (or lack thereof) with light.
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