EPR-SPECTRA FROM EPR-SILENT SPECIES - HIGH-FIELD EPR SPECTROSCOPY OF AQUEOUS CHROMIUM(II)

High-field (up to 14.5 T) multifrequency (similar to 90-440 GHz) elect ron paramagnetic resonance (EPR) spectroscopy has been used to probe t he non-Kramers, S = 2, Cr2+ ion in frozen aqueous solution, in the pre sence and absence of the glassing agent, glycerol. Solutions with both chloride and sulfate counterions were investigated. Detailed analysis based on a combination of analytical and full-matrix solutions to the spin Hamiltonian for an S = 2 system gave zero-field splitting parame ters D = -2.20(5) cm(-1), E = 0.0(1) cm(-1), and g(perpendicular to) a pproximate to g(parallel to) = 1.98(2), independent of solvent system and counterion. These results are in agreement with an early single-cr ystal EPR study of CrSO4. 5H(2)O; however, the present study allows un equivocal determination of the sign of D and shows that in solution [C r(H2O)(6)](2+) is a perfectly axial system (tetragonally elongated), a s opposed to solid CrSO4. 5H(2)O, which showed a measurable E value, i ndicative of slight orthorhombic distortion as seen in its crystal str ucture. HF-EPR data is combined with earlier electronic absorption dat a to provide a complete picture of the electronic structure of Cr2+ in this chemical environment. The results are also compared to a recent HF-EPR study of a Mn3+ complex, which showed that electronic excited s tates affect the ground state of the complex, but these effects are le ss pronounced for Cr2+. The present study also shows the applicability of high-field EPR to aqueous solutions of integer-spin (''EPR-silent' ') transition metal complexes, as previous studies have employed only solid (single-crystal or polycrystalline) samples.