Two relaxation processes of the magnetization in an antiferromagnetically coupled Dy ₂ metallacrown-based complex.

[U(Tp^Me2)₂I] exhibits at low temperatures single molecule magnet (SMM) behaviour comparable to its bipyridine derivative and related single ion U(III) complexes recently reported as SMMs. The trend of variation of the energy barrier for the magnetic relaxation in these compounds is well reproduced by quantum chemistry calculations.

It has been widely accepted in the past that the $g$ tensor describing the Zeeman splitting of a Kramers doublet is not uniquely defined. Here we show that with two basic requirements, (i) the invariance of the Zeeman Hamiltonian under symmetry transformations and (ii) its continuous change with the variations of the parameters of the system (geometry and crystal field), a unique determination of the elements of the $g$ tensor is achieved.