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Synthesis and Characterization of Barium Tetrafluoridobromate(III) Ba(BrF 4 ) 2
Author(s) -
Ivlev Sergey,
Sobolev Vasily,
Hoelzel Markus,
Karttunen Antti J.,
Müller Thomas,
Gerin Ivan,
Ostvald Roman,
Kraus Florian
Publication year - 2014
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.201402849
Subject(s) - chemistry , raman spectroscopy , barium , alkali metal , tetragonal crystal system , alkaline earth metal , microcrystalline , crystallography , powder diffraction , x ray crystallography , crystal structure , analytical chemistry (journal) , inorganic chemistry , diffraction , organic chemistry , physics , optics
Alkali and alkaline earth metal tetrafluoridobromates M I BrF 4 , M II (BrF 4 ) 2 (M I = Na–Cs, M II = Sr, Ba) can be synthesized from the respective fluorides and BrF 3 . The reaction of BaF 2 with liquid BrF 3 under Freon‐113 leads to the formation of Ba(BrF 4 ) 2 as a colorless microcrystalline powder. Here, we discuss its formation kinetics and thermodynamics. The compound crystallizes in the tetragonal space group I $\bar {4}$ with a = 9.65081(11) Å, c = 8.03453(13) Å, V = 748.32(2) Å 3 , and Z = 4 at 27 °C, and it is isotypic to Ba(AuF 4 ) 2 . The structure contains square planar BrF 4 – anions. The compound is stable at ambient conditions excluding moisture and at temperatures up to approximately 200 °C. Solid‐state computational calculations of the Raman and IR spectra are in good agreement with the experimentally obtained ones, and in combination with its powder X‐ray diffraction pattern, density measurement, thermodynamics, elemental and EDXRF analyses, this shows that the compound is pure.