دورية أكاديمية
[Se(CH2C(O)CH3)3][B12F11NH3]: The first selenium cation with three β-ketone substituents
العنوان: | [Se(CH2C(O)CH3)3][B12F11NH3]: The first selenium cation with three β-ketone substituents |
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المؤلفون: | Carsten Jenne, Marc C. Nierstenhöfer |
المصدر: | Acta Crystallographica Section E: Crystallographic Communications, Vol 76, Iss 2, Pp 221-224 (2020) |
بيانات النشر: | International Union of Crystallography, 2020. |
سنة النشر: | 2020 |
المجموعة: | LCC:Crystallography |
مصطلحات موضوعية: | crystal structure, selenium cation, weakly coordinating anion, dodecaborates, boron cluster, c—h activation, Crystallography, QD901-999 |
الوصف: | The reaction of [Se8][B12F11NH3]2 with acetone and subsequent crystallization from acetone/diethyl ether yielded the selenium cation [Se(CH2C(O)CH3)3]+ as a by-product, which is stabilized by the weakly coordinating undecafluorinated anion [B12F11NH3]−. While attempting to crystallize pure [Se8][B12F11NH3]2, the structure of the isolated product, namely, tris(2-oxopropyl)selenium 1-ammonioundecafluorododecaborate, was surprising. The cation [Se(CH2C(O)CH3)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 C3 symmetry and forms hydrogen bonds to the ammonio group of the anion. |
نوع الوثيقة: | article |
وصف الملف: | electronic resource |
اللغة: | English |
تدمد: | 2056-9890 20569890 |
Relation: | http://scripts.iucr.org/cgi-bin/paper?S2056989020000481; https://doaj.org/toc/2056-9890 |
DOI: | 10.1107/S2056989020000481 |
URL الوصول: | https://doaj.org/article/73e7c1d56b08413a80a87e6485c5d3b5 |
رقم الأكسشن: | edsdoj.73e7c1d56b08413a80a87e6485c5d3b5 |
قاعدة البيانات: | Directory of Open Access Journals |
تدمد: | 20569890 |
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DOI: | 10.1107/S2056989020000481 |