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Systematic Investigation of the Nature of The Coupling between a Ln(III) Ion (Ln = Ce(III) to Dy(III)) and Its Aminoxyl Radical Ligands. Structural and Magnetic Characteristics of a Series of {Ln(organic radical)<sub>2</sub>} Compounds and the Related {Ln(Nitrone)<sub>2</sub>} Derivatives

393

Citations

19

References

2000

Year

Abstract

Numerous molecular compounds in which a paramagnetic Ln(III) ion is in interaction with a second spin carrier such as a transition metal ion or an organic radical have been described. However, except for the isotropic Gd(III) ion, very little is known concerning the nature (ferro- or antiferromagnetic) and mechanism of the interaction involving a Ln(III) ion. This study addresses the problem of the interaction between the Ln(III) ions displaying spin−orbit coupling and an organic radical. The magnetic properties of a series of isostructural compounds, {Ln(organic radical)2(NO3)3}, comprising a Ln(III) ion (Ln = Ce to Dy) surrounded by two N,O-chelating aminoxyl radicals (3-nitronyl nitroxide-4,5-dimethyltriazole) have been investigated. The experimental approach used to get insight into the {Ln-Radical} coupling occurring within these compounds is based on the knowledge of the intrinsic paramagnetic contribution of the metal ion. This contribution has been deduced from the corresponding {Ln(Nitrone)2(NO3)3} derivatives (Nitrone stands for 3-N-tert-butylnitrone-4,5-dimethyltriazole), where the Ln(III) ion is now in a diamagnetic surrounding. A simple mathematical difference of the magnetic susceptibilities of {Ln(organic radical)2(NO3)3} and the corresponding {Ln(Nitrone)2(NO3)3} derivatives then permitted the nature of the correlations within the {Ln(organic radical)2(NO3)3} compounds to be established. Moreover, these results have been confirmed by the field dependence of the magnetization for each derivative. A systematic investigation of the isostructural series of compounds allowed the evolution of these interactions to be compared as a function of the electronic configuration of the 4f orbitals. For the Ln(III) with 4f1 to 4f5 electronic configurations the {Ln-organic radical} interaction is antiferromagnetic. Conversely, this interaction was found to be ferromagnetic for the configurations 4f7 to 4f.10 These interactions have been clearly indicated for each Ln(III).

References

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