Donor‐unsupported Phosphanylmethanides Li[CH2PR2] (R = tBu,Ph) – Crystal Structure of Li[CH2PtBu2] Solved by XRPD and DFT‐D Calculations |
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| Authors: | Lothar Fink Kamil Samigullin Alexander Bodach Edith Alig Matthias Wagner Hans‐Wolfram Lerner |
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| Affiliation: | Institut für Anorganische Chemie,Goethe‐Universit?t Frankfurt, Max‐von‐Laue‐Str. 7, 60438 Frankfurt, Germany |
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| Abstract: | The solvent‐free methyllithium derivatives LiCH2PR2] (R = tBu, Ph) were prepared via the reaction of CH3PR2 with LitBu]. It should be noted that the deprotonation of CH3PtBu2 with LitBu] occurred at 60 °C, whereas LiCH2PPh2] was already formed from CH3PPh2 with LitBu] at ambient temperature. The structure determination of di‐tert‐butylphosphanylmethyllithium was performed by high resolution X‐ray powder diffraction analysis at different temperatures. This led to two possible structure solutions with similar quality criteria (space groups Iba2 and I2/a). Therefore CASTEP DFT‐D calculations were applied to verify the correct crystal structure. The solid‐state structure of di‐tert‐butylphosphanylmethyllithium consists of alternating edge‐sharing six‐ and four‐membered rings, which form a polymeric, infinite double‐chain along the crystallographic c axis in the monoclinic space group I2/a. Two LiCH2PtBu2] units connected via an inversion center form a six‐membered Li2C2P2 ring in the chair conformation. The nearly flat four‐membered Li2C2 ring, is oriented perpendicularly to the twofold axis. |
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| Keywords: | Organolithium compounds Phosphorus X‐ray powder diffraction DFT‐D CASTEP |
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