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Université de Fribourg

Self-assembly of Ag(I) helicates with new enantiopure 5,6-Chiragen type ligands

Mamula, Olimpia ; Bark, Thomas ; Quinodoz, Boris ; Stoeckli-Evans, Helen ; Zelewsky, Alexvon

In: Inorganica Chimica Acta, 2018, vol. 475, p. 200–206

Two new chiral bis-bidentate, C2-symmetrical ligands belonging to the Chiragen family have been synthesised and characterised. They are designed for polynuclear self-assemblies since the two (−)-5,6-pinenebipyridines units are connected by bridges whose length and rigidity avoids the coordination of the bipyridine moieties to the same metal centre. The ligand L1 with a 1,4-dimethylene...

Université de Fribourg

Crystal structures of trans-di­chlorido­tetra­kis­[1-(2,6-diiso­propyl­phen­yl)-1H-imidazole-ΚN³]iron(II), trans-di­bromido­tetra­kis­[1-(2,6-diiso­propyl­phen­yl)-1H-imidazole-ΚN³]iron(II) and trans-di­bromido­tetra­kis­[1-(2,6-diiso­propyl­phen­yl)-1H-imidazole-ΚN³]iron(II) diethyl ether disolvate

Mafua, Roger ; Jenny, Titus ; Labat, Gael ; Neels, Antonia ; Stoeckli-Evans, Helen

In: Acta Crystallographica Section E Structure Reports Online, 2014, vol. 70, no. 8, p. 72–76

The title compounds, [FeCl₂(C₁₅H₂₀N₂)₄], (I), [FeBr₂(C₁₅H₂₀N₂)₄], (II), and [FeBr₂(C₁₅H₂₀N₂)₄]·2C₄H₁₀O, (IIb), respectively, all have triclinic symmetry, with (I) and (II) being isotypic. The FeII atoms in each of the structures are located on an inversion center. They have octa­hedral FeX₂N₄ (X = Cl and Br,...

Université de Fribourg

A family of immobilizable chiral bis(pinenebipyridine) ligands

Pöllnitz, Alpár ; Skupienski, Radek ; Stoeckli-Evans, Helen ; Crochet, Aurélien ; Silvestru, Anca ; Fromm, Katharina M. ; Mamula, Olimpia

In: Synlett, 2013, vol. 24, no. 19, p. 2555–2558

New enantiopure ligands containing two (–)-5,6-pinenebipyridine units connected by a bridge situated in position 6′ of the bipyridines have been prepared. The chemically addressable groups of the bridging (hydroxyl or keto) can be covalently bound to various supports in order to heterogenize the ligand.

Université de Fribourg

Probing intermetallic coupling in dinuclear N-heterocyclic carbene ruthenium(II) complexes

Mercs, Laszlo ; Neels, Antonia ; Stoeckli-Evans, Helen ; Albrecht, Martin

In: Inorganic Chemistry, 2011, vol. 50, no. 17, p. 8188–8196

A series of bimetallic N-heterocyclic carbene (NHC) ruthenium(II) complexes were synthesized, which comprise two [RuCl₂(cymene)(NHC)] units that are interlinked via the NHC nitrogens by alkyl chains of different length. Electrochemical characterization revealed two mutually dependent oxidation processes for the complex with a methylene linker, indicating moderate intramolecular electronic...

Université de Neuchâtel

Optically active liquid-crystalline fullerodendrimers from enantiomerically pure fulleropyrrolidines

Lincker, Frédéric ; Bourgun, Philippe ; Stoeckli-Evans, Helen ; Saez, Isabel M. ; Goodby, John W. ; Deschenaux, Robert

In: Chemical Communications, 2010, vol. 46, no. 40, p. 7522-7524

A synthetic methodology based on the 1,3-dipolar cycloaddition reaction was developed to design enantiomerically pure liquid-crystalline fullerodendrimers.

Université de Fribourg

Synthesis and tunability of abnormal 1,2,3-triazolylidene palladium and rhodium complexes

Poulain, Aurélie ; Canseco-Gonzalez, Daniel ; Hynes-Roche, Rachel ; Müller-Bunz, Helge ; Schuster, Oliver ; Stoeckli-Evans, Helen ; Antonia Neels ; Albrecht, Martin

In: Organometallics, 2011, vol. 30, no. 5, p. 1021–1029

Palladation of N3-alkylated 1,2,3-triazolium salts with Pd(OAc)₂ afforded a μ²−I₂ bridged bimetallic complex [Pd(trz)I₂]₂ and monometallic bis(carbene) complexes Pd(trz)₂I₂ as a mixture of trans and cis isomers (trz = 1,2,3-triazol-5-ylidene). Addition of excess halide or modification of the palladation procedure from direct functionalization to a transmetalation...

Université de Neuchâtel

Catalytic Hydrogenation of meso-Octamethylporphyrinogen (Calix[4]pyrrole)

Journot, Guillaume ; Letondor, Christophe ; Neier, Reinhard ; Stoeckli-Evans, Helen ; Savoia, Diego ; Gualandi, Andrea

In: Chemistry - A European Journal, 2010, vol. 16, no. 4, p. 4224-4230

Hydrogenation of meso-octamethylporphyrinogen (calix[4]pyrrole) with a number of heterogeneous catalysts under different experimental conditions has been investigated. GC-MS analyses of the reaction mixtures showed the formation of one to four products in low to moderate yields: three of them were diastereoisomers of the product derived from half-hydrogenation of the substrate, and displayed...