Jm. Forward et al., SYNTHESIS AND MAGNETIC STUDIES OF THE METALLOCARBORANE SANDWICH SALTS[FE(C(5)ME(5))(2)][M(C2B9H12)(2))] (M=CR,FE,NI), Journal of organometallic chemistry, 465(1-2), 1994, pp. 251-258
The salts [Fe(C(5)Me(5))(2)][M(C2B9H11)(2))], (M = Cr, Fe, Ni), have b
een prepared by metathesis of [Fe(C(5)Me(5))(2)]Cl and [(CH3)(4)N][M(C
2B9H11)(2))], (M = Cr, Fe, Ni), and the three salts have been shown to
be isostructural from powder X-ray diffraction studies. The structure
of the salt [Fe(C(5)Me(5))(2)][Fe(C2B9H11)(2))] has been determined b
y a single crystal X-ray diffraction study. The anions and cations pac
k in a distorted CsCl-type structure in which the distortion is though
t to arise from the non-spherical shape of the [Fe(C2B9H11)(2))](-) an
ion. The sold-state magnetic susceptibility data for all three salts c
an be fitted to the Curie-Weiss law between 6 and 296 K. Low values of
theta indicate there are no significant ferromagnetic or antiferromag
netic interactions between the unpaired spins, even at low temperature
s.