Ellwanger Mathias A, Steinhauer Simon, Golz Paul, Braun Thomas, Riedel Sebastian
Freie Universität Berlin, Institut für Chemie und Biochemie, Fabeckstrasse 34/36, 14195, Berlin, Germany.
Humboldt-Universität zu Berlin, Department of Chemistry, Brook-Taylor-Strasse 2, 12489, Berlin, Germany.
Angew Chem Int Ed Engl. 2018 Jun 11;57(24):7210-7214. doi: 10.1002/anie.201802952. Epub 2018 May 14.
Two different reaction routes are described to access the unprecedented trifluoridoorganogold(III) complex [AuF (SIMes)]. The compound bears the N-heterocyclic carbene SIMes (1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidene) as a ligand for a molecular Lewis acidic AuF unit and was characterized by NMR spectroscopy as well as X-ray crystallography. Apart from the use of a [AuF ] salt as precursor, the strong oxidizing compound AuF can be employed neat as starting material. The reaction proceeded even in organic solvents in the presence of SIMes as the ligand precursor. Decomposition reactions with the solvent can, therefore, be prevented by using this strategy.
描述了两种不同的反应路线来制备前所未有的三氟有机金(III)配合物[AuF (SIMes)]。该化合物带有N-杂环卡宾SIMes(1,3-双(2,4,6-三甲基苯基)-4,5-二氢咪唑-2-亚基)作为分子路易斯酸性AuF单元的配体,并通过核磁共振光谱以及X射线晶体学进行了表征。除了使用[AuF ]盐作为前体之外,强氧化性化合物AuF可以直接用作起始原料。即使在有机溶剂中,以SIMes作为配体前体时反应也能进行。因此,通过使用这种策略可以防止与溶剂发生分解反应。