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Diaryltin Dihydrides and Aryltin Trihydrides with Intriguing Stability

In the last few decades, organotin hydrides have proven their potential as building blocks for a great variety of organometallic compounds. In this context, organotin hydrides with sterically shielding aryl substituents have attracted special interest, as these ligands can kinetically stabilize meta...

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Detalles Bibliográficos
Autores principales: Steller, Beate G., Doler, Berenike, Fischer, Roland C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7179233/
https://www.ncbi.nlm.nih.gov/pubmed/32121022
http://dx.doi.org/10.3390/molecules25051076
Descripción
Sumario:In the last few decades, organotin hydrides have proven their potential as building blocks for a great variety of organometallic compounds. In this context, organotin hydrides with sterically shielding aryl substituents have attracted special interest, as these ligands can kinetically stabilize metastable products. The selective synthesis of aryltin halide compounds Ar*(2)SnCl(2) and Ar*SnI(3) featuring the highly sterically encumbered aryl ligand Ar* ((i)(Pr)Ar* = 2,6-(Ph(2)CH)(2)-4-iPrC(6)H(2); (Me)Ar* = 2,6-(Ph(2)CH)(2)-4-MeC(6)H(2)) is presented. These aryltin halides were converted into corresponding aryltin hydrides Ar*(2)SnH(2) and Ar*SnH(3), which exhibit a surprisingly high thermal stability and oxygen tolerance.