Abstract
The reactivity of the frustrated Lewis pair (FLP) (F5C2)3SnCH2P(tBu)2 (1) was investigated with respect to the activation of elemental hydrogen. The reaction of 1 at elevated hydrogen pressure afforded the intramolecular phosphonium stannate(II) (F5C2)2SnCH2PH(tBu)2 (3). It was characterized by means of multinuclear NMR spectroscopy and single crystal X-ray diffraction. NMR experiments with the two isotopologues H2 and D2 showed it to be formed via an H2 adduct (F5C2)3HSnCH2PH(tBu)2 (2) and the subsequent formal reductive elimination of pentafluoroethane; this is supported by DFT calculations. Parahydrogen-induced polarization experiments revealed the formation of a second product of the reaction of 1 with H2, [HP(tBu)2Me][Sn(C2F5)3] (4), in 1H NMR spectra, whereas 2 was not detected due to its transient nature.
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Holtkamp, P., Schwabedissen, J., Neumann, B., Stammler, H. G., Koptyug, I. V., Zhivonitko, V. V., & Mitzel, N. W. (2020). A Zwitterionic Phosphonium Stannate(II) via Hydrogen Splitting by a Sn/P Frustrated Lewis-Pair and Reductive Elimination. Chemistry - A European Journal, 26(72), 17381–17385. https://doi.org/10.1002/chem.202004425
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