In: Journal of the American Chemical Society, 2008, vol. 130, no. 41, p. 13534–13535
The [3 + 2] cycloaddition of azides and acetylenes followed by nitrogen quaternization was applied for the generation of novel and highly modular triazolium salts. The selective substitution of the 1,3,4-substitution pattern presets such salts as precursors for a new class of abnormal carbene ligands, thus expanding the family of these high-impact ligands. Metalation of the triazolium salts is...
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In: Journal of Chemical Crystallography, 2003, vol. 33, no. 1, p. 39-50
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In: ChemCatChem, 2011, vol. 3, no. 1, p. 167-173
Palladium complexes containing abnormally bound C4-bound dicarbene ligands have been exploited for catalytic alkene hydrogenation. Comparison to normally C2-bound homologues indicates that the carbene bonding mode critically influences the catalytic activity. Good catalytic performance in the hydrogenation of cis-disubstituted olefins and non-isomerizable terminal olefins under mild...
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In: European Journal of Inorganic Chemistry, 2012, p. -
Oxidative addition of donor-functionalised 4-iodoimidazolium salts to palladium(0) provides a selective route for the preparation of abnormal chelating N-heterocyclic carbene complexes and enables the introduction of a variety of donor groups. The activation of the C4 position does not necessitate protection of the imidazolium C2 position, thereby leaving this site available for further...
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In: Organometallics, 2009, vol. 28, no. 17, p. 5112–5121
A series of ruthenium(II) complexes have been prepared by using bidentate chelating N-heterocyclic carbene (NHC) ligands that feature different donor groups E (E = olefin, thioether, carboxylate, and NHC). Rigid coordination of all donor sites was concluded from NMR spectroscopy, and the electronic impact of the donor group was evaluated by electrochemical analyses. The chelating donor group had...
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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,...
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In: New Journal of Chemistry, 2009, vol. 33, p. 462–465
Chiral bis-5,6-pinene bipyridine type ligands have been used to form, through self-assembly reaction, dinuclear coordination compounds which show a highly diastereoselective formation of double helices with copper(I) and silver(I) as coordination centers.
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In: Dalton Transactions, 2004, vol. 3, p. 402-406
The enantiomerically pure chiral tris-chelating ligand (+)-(7S,10R)-L(L) comprising three 4,5-pinenobipyridine subunits connected through a mesityl spacer has been synthesized. Complexes of L with RuII and FeII have been prepared and characterised. NMR spectroscopy indicates that...
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In: Polyhedron, 2004, vol. 23, no. 6, p. 1011-1017
The zinc(II) complexes 1aZnCl₂ and 1bZnCl₂ (1a: 2-(6',2''-bipyrid-2'-yl)-3-(2- pyridyl)pyrazine; 1b: 2-(6',2'-bipyrid-2'-yl)-5,6-dinitrilo-3-(2-pyridyl)pyrazine) were prepared by treatment of the ligands with ZnCl₂. The structures of both were investigated by X-ray crystallography and 1H NMR spectroscopy. Both complexes display proton deshielding phenomena that are attributed to a...
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In: Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2008, vol. 61, no. 1-2, p. 127-130
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