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Abstract:
Two monochromium(III)-containing heteropolytungstates, [CrIII(HPVW7O28)2]13- (1a) and [CrIII(HAsVW7O28)2]13- (2a), were prepared via simple, one-pot reactions in aqueous, basic medium, by reaction of the composing elements, and then isolated as hydrated sodium salts, Na13[CrIII(HPVW7O28)2]·47H2O (1) and Na13[CrIII(HAsVW7O28)2]·52H2O (2). Polyanions 1a and 2a comprise an octahedrally coordinated CrIII ion, sandwiched by two {PW7} or {AsW7} units. Both compounds 1 and 2 were fully characterized in the solid state by single-crystal XRD, IR spectroscopy, thermogravimetric and elemental analyses, magnetic susceptibility, and EPR measurements. Magnetic studies on 1 and 2 demonstrated that both compounds exhibit appreciable deviation from typical paramagnetic behavior, and have a ground state S = 3/2, as expected for a CrIII ion, but with an exceptionally large zero-field uniaxial anisotropy parameter (D). EPR measurements on powder and single-crystal samples of 1 and 2 using 9.5, 34.5, and 239.2 GHz frequencies and over 4–295 K temperature fully support the magnetization results and show that D = +2.4 cm–1, the largest and sign-assigned D-value so far reported for an octahedral CrIII-containing, molecular compound. Ligand field analysis of results from CASSCF and NEVPT2-correlated electronic structure calculations on Cr(OH)63– model complexes allowed to unravel the crucial role of the second coordination sphere of CrIII for the unusually large magnetic anisotropy reflected by the experimental value of D. The newly developed theoretical modeling, combined with the synthetic procedure for producing such unusual magnetic molecules in a well-defined and essentially magnetically isolated environment, appears to be a versatile new research area.
