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Phosphanylalanes and Phosphanylgallanes Stabilized only by a Lewis Base

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⋅GaH(2)PCy(2) (1) (IDipp=1,3‐bis(2,6‐diisopropylphenyl)‐imidazolin‐2‐ylidene) were obtained by the rea...

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Detalles Bibliográficos
Autores principales: Weinhart, Michael A. K., Lisovenko, Anna S., Timoshkin, Alexey Y., Scheer, Manfred
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155101/
https://www.ncbi.nlm.nih.gov/pubmed/31815355
http://dx.doi.org/10.1002/anie.201914046
Descripción
Sumario: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⋅GaH(2)PCy(2) (1) (IDipp=1,3‐bis(2,6‐diisopropylphenyl)‐imidazolin‐2‐ylidene) were obtained by the reaction of LiPCy(2) with IDipp⋅GaH(2)Cl. However, the LB‐stabilized parent compounds IDipp⋅GaH(2)PH(2) (3) and IDipp⋅AlH(2)PH(2) (4) were prepared via a salt metathesis of LiPH(2)⋅DME with IDipp⋅E′H(2)Cl (E′=Ga, Al) or by H(2)‐elimination reactions of IDipp⋅E′H(3) (E′=Ga, Al) and PH(3), 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.