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Synthesis of a 1-Aryl-2,2-chlorosilyl(phospha)silene Coordinated by an N-Heterocyclic Carbene †

Phosphasilenes, P=Si doubly bonded compounds, have received considerable attention due to their unique physical and chemical properties. We report on the synthesis and structure of a chlorophosphasilene coordinated by an N-heterocyclic carbene (NHC), which has the potential of functionalization at t...

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Detalles Bibliográficos
Autores principales: Kyri, Andreas Wolfgang, Majhi, Paresh Kumar, Sasamori, Takahiro, Agou, Tomohiro, Nesterov, Vitaly, Guo, Jing-Dong, Nagase, Shigeru, Tokitoh, Norihiro, Streubel, Rainer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274381/
https://www.ncbi.nlm.nih.gov/pubmed/27706036
http://dx.doi.org/10.3390/molecules21101309
Descripción
Sumario:Phosphasilenes, P=Si doubly bonded compounds, have received considerable attention due to their unique physical and chemical properties. We report on the synthesis and structure of a chlorophosphasilene coordinated by an N-heterocyclic carbene (NHC), which has the potential of functionalization at the Si–Cl moiety. Treatment of a silylphosphine, ArPH–SiCl(2)R(Si) (Ar = bulky aryl group, R(Si) = Si(SiMe(3))(3)) with two equivalents of Im-Me(4) (1,3,4,5-tetramethylimidazol-2-ylidene) afforded the corresponding NHC-coordinated phosphasilene, ArP=SiClR(Si)(Im-Me(4)) as a stable compound. Bonding properties of the P=Si bond coordinated to an NHC will be discussed on the basis of theoretical calculations.