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Preparation and Reactivity of a Triphosphenium Bromide Salt: A Convenient and Stable Source of PhosphorusI
Published on: November 22, 2016
Phosphanylalanes and Phosphanylgallanes Stabilized only by a Lewis Base
Michael A K Weinhart1, Anna S Lisovenko2, Alexey Y Timoshkin2
1Institut für Anorganische Chemie, Universität Regensburg, 93040, Regensburg, Germany.
Abstract:
The synthesis and characterization of the first parent phosphanylalane and phosphanylgallane stabilized only by a Lewis base (LB) are reported. The corresponding substituted compounds, such as IDipp⋅GaH2 PCy2 (1) (IDipp=1,3-bis(2,6-diisopropylphenyl)-imidazolin-2-ylidene) were obtained by the reaction of LiPCy2 with IDipp⋅GaH2 Cl. However, the LB-stabilized parent compounds IDipp⋅GaH2 PH2 (3) and IDipp⋅AlH2 PH2 (4) were prepared via a salt metathesis of LiPH2 ⋅DME with IDipp⋅E'H2 Cl (E'=Ga, Al) or by H2 -elimination reactions of IDipp⋅E'H3 (E'=Ga, Al) and PH3 , respectively. The compounds could be isolated as crystalline solids and completely characterized. Supporting DFT computations gave insight into the reaction pathways as well as into the stability of these compounds with respect to their decomposition behavior.
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