Title of article :
[Se(CH2C(O)CH3)3][B12F11NH3]: The first selenium cation with three β-ketone substituents
Author/Authors :
Jenne, Carsten Anorganische Chemie - Fakultät für Mathematik und Naturwissenschaften - Bergische Universität Wuppertal, Germany , Nierstenhöfer, Marc C. Anorganische Chemie - Fakultät für Mathematik und Naturwissenschaften - Bergische Universität Wuppertal, Germany
Abstract :
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.
Keywords :
crystal structure , selenium cation , weakly coordinating anion , dodecaborates , boron cluster
Journal title :
Acta Crystallographica Section E: Crystallographic Communications