Reductive Elimination and Oxidative Addition of Hydrogen at Organostannylium and Organogermylium Cations |
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Authors: | Fatima Diab Frederik S. W. Aicher Dr. Christian P. Sindlinger Dr. Klaus Eichele Dr. Hartmut Schubert Prof. Dr. Lars Wesemann |
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Affiliation: | 1. Institut für Anorganische Chemie, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 18, 72076 Tübingen, Germany;2. Institut für Anorganische Chemie, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 18, 72076 Tübingen, Germany Institut für Anorganische Chemie, Georg-August Universität Göttingen, Tammannstr. 4, 37077 Göttingen, Germany |
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Abstract: | Bulkily substituted organodihydrogermylium and -stannylium cations [Ar*EH2]+ (E=Ge, Sn; Ar*=2,6-Trip2C6H3, Trip=2,4,6-triisopropylphenyl) were characterized as salts of the weakly coordinating perfluorinated alkoxyaluminate anion [Al{OC(CF3)3}4]−. At room temperature, the stannylium cation liberates hydrogen to generate the low valent organotin cation [Ar*Sn]+. In contrast, the dihydrogermylium cation transfers the hydrogen atoms to an aryl moiety of the terphenyl ligand and oxidatively adds either hydrogen under an atmosphere of hydrogen or a sp2 CH unit of the 1,2-difluorobenzene solvent. |
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Keywords: | germylium cation hydrogen activation oxidative addition reductive elimination stannylium cation |
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