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[Se(CH(2)C(O)CH(3))(3)][B(12)F(11)NH(3)]: The first selenium cation with three β-ketone substituents

The reaction of [Se(8)][B(12)F(11)NH(3)](2) with acetone and subsequent crystallization from acetone/diethyl ether yielded the selenium cation [Se(CH(2)C(O)CH(3))(3)](+) as a by-product, which is stabilized by the weakly coordinating undeca­fluorinated anion [B(12)F(11)NH(3)](−). While attempting to...

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Detalles Bibliográficos
Autores principales: Jenne, Carsten, Nierstenhöfer, Marc C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7001834/
https://www.ncbi.nlm.nih.gov/pubmed/32071750
http://dx.doi.org/10.1107/S2056989020000481
Descripción
Sumario:The reaction of [Se(8)][B(12)F(11)NH(3)](2) with acetone and subsequent crystallization from acetone/diethyl ether yielded the selenium cation [Se(CH(2)C(O)CH(3))(3)](+) as a by-product, which is stabilized by the weakly coordinating undeca­fluorinated anion [B(12)F(11)NH(3)](−). While attempting to crystallize pure [Se(8)][B(12)F(11)NH(3)](2), the structure of the isolated product, namely, tris­(2-oxoprop­yl)selenium 1-ammonio­undeca­fluoro­dodeca­borate, was surprising. The cation [Se(CH(2)C(O)CH(3))(3)](+) represents the first example for a cationic selenium compound with three ketone functional groups located in the β-position with respect to the selenium atom. The cation possesses almost trigonal–pyramidal C (3) symmetry and forms hydrogen bonds to the ammonio group of the anion.