4.7 Article

Crystal Growth from Anhydrous HF Solutions of M2+ (M = Ca, Sr, Ba) and [AuF6]-, Not Only Simple M(AuF6)2 Salts

Journal

INORGANIC CHEMISTRY
Volume 61, Issue 27, Pages 10587-10597

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.2c01675

Keywords

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Funding

  1. Slovenian Research Agency [P1-0045]
  2. Inorganic Chemistry and Technology

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Crystal growth from anhydrous HF solutions of M2+ (M = Ca, Sr, Ba) and [AuF6]- (molar ratio 1:2) produced various compounds with different crystal structures. The crystal structures exhibit diversity, including layered structure and three-dimensional networks. It is found that the previously reported compounds M(AuF6)(2) do not correspond to the reported chemical formula. Additionally, crystal structures of some byproducts were observed.
Crystal growth from anhydrous HF solutions of M2+ (M = Ca, Sr, Ba) and [AuF6]- (molar ratio 1:2) gave [Ca(HF)(2)](AuF6)(2), [Sr(HF)]-(AuF6)(2), and Ba[Ba(HF)](6)(AuF6)(14). [Ca(HF)(2)](AuF6)(2) exhibits a layered structure in which [Ca(HF)(2)](2+) cations are connected by AuF6 units, while the crystal structure of Ba[Ba(HF)](6)(AuF6)(14) exhibits a complex three-dimensional (3-D) network consisting of Ba2+ and [Ba(HF)(2)](2+) cations bridged by AuF6 groups. These results indicate that the previously reported M(AuF6)(2) (M = Ca, Sr, Ba) compounds, prepared in the anhydrous HF, do not in fact correspond to this chemical formula. When the initial M2+/ [AuF6](-) ratio was 1:1, single crystals of [M(HF)](H3F4)(AuF6) were grown for M = Sr. The crystal structure consists of a 3-D framework formed by [Sr(HF)](2+) cations associated with [AuF6]- and [H3F4](-) anions. The latter exhibits a Z-shaped conformation, which has not been observed before. Single crystals of M(BF4)(AuF6) (M = Sr, Ba) were grown when a small amount of BF3 was present during crystallization. Sr(BF4)(AuF6) crystallizes in two modifications. A high-temperature alpha-phase (293 K) crystallized in an orthorhombic unit cell, and a low-temperature beta-phase (150 K) crystallized in a monoclinic unit cell. For Ba(BF4)(AuF6), only an orthorhombic modification was observed in the range 80-230 K. An attempt to grow crystals of Ca(BF4)(AuF6) failed. Instead, crystals of [Ca(HF)](BF4)(2) were grown and the crystal structure was determined. During prolonged crystallization of [AuF](6)- salts, moisture can penetrate through the walls of the crystallization vessel. This can lead to partial reduction of Au(V) to A(III) and the formation of [AuF4](-) byproducts, as shown by the single-crystal growth of [Ba(HF)](4)(AuF4)(AuF6)(7). Its crystal structure consists of [Ba(HF)](2+) cations connected by AuF6 octahedra and square-planar AuF4 units. The crystal structure of the minor product [O-2](2)[Sr(HF)]5[AuF6](12).HF was also determined.

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