Sh. Elder et al., SYNTHESIS OF AU(II) FLUORO COMPLEXES AND THEIR STRUCTURAL AND MAGNETIC-PROPERTIES, Journal of the American Chemical Society, 119(5), 1997, pp. 1020-1026
Gold at similar to 20 degrees C with F-2 in anhydrous hydrogen fluorid
e (aHF) acidified with SbF5 dissolves to a red solution from which ora
nge Au-II(SbF6)(2) crystallizes on removal of volatiles. Au(SbF6)(2) i
s triclinic with a=5.300(1) Angstrom, b=5.438(1) Angstrom, c=8.768(2)
Angstrom, alpha=76.872(3)degrees, beta=88.736(3)degrees, gamma=68.109(
3)degrees, V=227.79(7) Angstrom(3), and Z=1, space group <P(1)over bar
>. Each Au(II) atom, at (1) over bar, is at the center of an elongated
octahedron of F ligands; the four F's of the approximately square AuF
4 unit are at 2.09(2) Angstrom x2 Angstrom and 2.15(2) Angstrom x2, ea
ch F provided by a different SbF6 species. The two long Au-F interatom
ic distances are at 2.64(2) Angstrom. The SbF6 are grossly distorted i
n their interactions with the Au. A cis pair of F ligands of each SbF6
, make close approach to two different gold atoms, stretching Sb-F to
1.99(2) and 1.94(2) Angstrom. In each case the Sb-F distances trans to
these stretched Sb-F bonds are short,being 1.85(2) and 1.84(2) Angstr
om, respectively. Magnetic susceptibility measurements show antiferrom
agnetic coupling with a susceptibility decrease below 13 K. Solvolysis
of Au-II(SbF6)(2) in aHF is accompanied by disproportionation: 4Au(Sb
F6)(2)-->Au+Au3F8+8SbF(5)(solv). Fluorination, at similar to 20 degree
s C, of the solution of Au(SbF6)(2), in SbF5 acidified aHF, precipitat
es red crystals of triclinic Au-II{SbF6}Au-2(II){(AuF4)-F-III}(2) with
a(o)=5.2345(2) Angstrom, b(o)=8.1218(1) Angstrom, c(o)=10.5977(3) Ang
strom, alpha=100.090(2)degrees, beta=100.327(2)degrees, gamma=104.877(
2)degrees, V=416.63(2) Angstrom(3), space group <P(1)over bar>, and Z=
1. It is a simple paramagnet. The structure shows two different Au(II)
environments, each approximately square-coordinated by F ligands, one
being coordinated trans by an F ligand of each of two SbF6 and simila
rly by an F ligand from each of two (AuF4)-F-III species. The other Au
(II) is approximately square-coordinated via bridging F ligands to fou
r different (AuF4)-F-III species. Au-II{SbF6}Au-2(II){(AuF4)-F-III}(2)
with KAuF4 in aHF yields Au3F8 free of metallic gold,the simple param
agnetism of which indicates the formulation Au-II{(AuF4)-F-III}(2).