The Absolute Best Science Experiment for Tris(dimethylamino)phosphine

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Quality Control of: Tris(dimethylamino)phosphine
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Chemistry is an experimental science, and the best way to enjoy it and learn about it is performing experiments.Introducing a new discovery about 1608-26-0, Name is Tris(dimethylamino)phosphine
, Quality Control of: Tris(dimethylamino)phosphine
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A versatile reactivity from the cage compound P(NMeNMe)3P is presented. The Staudinger reaction with Me3SiN3 is carried out. The crystal structure of the compound issued from the reaction on both sides (Me3SiN=P(NMeNMe)3P=NSiMe3) is reported. When the reaction occurs on only one side, the remaining free phosphorus atom is complexed with RuCl2(p-cymene). P(NMeNMe)3P reacts with PCl3, leading to the heterocyclic compound ClP(NMeNMe)2PCl. This heterocycle also displays a versatile reactivity. Substitution reaction with HNiPr2 leads to iPr2NP(NMeNMe)2PNiPr2. Very complex 1H and 13C NMR spectra suggest that the cis isomer is the largely major isomer of this compound. The cis structure is confirmed by X-ray diffraction. Besides the reaction on the P?Cl functions, the reaction on the lone pair of ClP(NMeNMe)2PCl is carried out, leading to the complex (p-cymene)Cl2RuPCl(NMeNMe)2ClPRuCl2(p-cymene). Characterization of this compound by X-ray diffraction displays a cis isomer for this compound also.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.Quality Control of: Tris(dimethylamino)phosphine
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Reference:
Phosphine ligand,
Chiral phosphine ligands in asymmetric synthesis. Molecular structure and absolute configuration of (1,5-cyclooctadiene)-(2S,3S)-2,3-bis(diphenylphosphino)butanerhodium(I) perchlorate tetrahydrofuran solvate