Abstract
The synthesis, crystal growth, and polarized optical absorption spectra in the visible and near-UV of (Et4N)3Cr2F9 are reported. In the energy range 25800-27700 cm(-1) the 4A2 --> 2A1 (O notation) ligand field transition can be resolved in detail for the first time in any Cr3+ compound. This allows the determination of the antiferromagnetic ground-state exchange splitting with great accuracy: J = 25.9 cm(-1) and j = 0.27 cm(-1) using the Hamiltonian H = J(S(A).S(B)) - j(S(A).S(B))2, where j leads to deviations from the regular Landé pattern. The temperature dependence of the magnetic susceptibility is nicely reproduced by these parameters. A comparison with Cs3Cr2Cl9 and Cs3Cr2Br9 reveals an exponential dependence of the ground-state splitting upon the Cr-Cr distance in the [Cr2X9]3- dimers. This is the result of a dominant sigma-type orbital exchange pathway along the Cr-Cr axis.
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