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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2020
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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 |
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. |
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