Rupf Susanne Margot, Pröhm Patrick, Malischewski Moritz
Freie Universität Berlin, Institut für Chemie und Biochemie, Institut für Anorganische Chemie, Fabeckstraße 34-36, 14195 Berlin, Germany.
Chem Commun (Camb). 2020 Aug 25;56(68):9834-9837. doi: 10.1039/d0cc04226a.
Instead of monomeric cyclopentadienyl cations, the low-temperature reaction of hexachloro- and hexabromocyclo-pentadiene (C5Cl6 and C5Br6) with powerful Lewis acids SbF5 and AsF5 in SO2ClF yields salts of perhalogenated dications [C10Cl10][Sb3F16]2 and [C10Br10][As2F11]2 which are characterized via single crystal X-ray diffraction and NMR spectroscopy. Additionally, this reactivity is rationalized by quantum-chemical calculations.
六氯环戊二烯(C5Cl6)和六溴环戊二烯(C5Br6)与强路易斯酸SbF5和AsF5在SO2ClF中进行低温反应,生成的不是单体环戊二烯阳离子,而是全卤代双阳离子盐[C10Cl10][Sb3F16]2和[C10Br10][As2F11]2,这些盐通过单晶X射线衍射和核磁共振光谱进行表征。此外,通过量子化学计算对这种反应活性进行了合理化解释。