دورية أكاديمية

[Se(CH2C(O)CH3)3][B12F11NH3]: The first selenium cation with three β-ketone substituents

التفاصيل البيبلوغرافية
العنوان: [Se(CH2C(O)CH3)3][B12F11NH3]: The first selenium cation with three β-ketone substituents
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
الوصف
تدمد:20569890
DOI:10.1107/S2056989020000481