Magnetic chains of Fe 3 clusters in the {Fe 3 YO 2 } butterfly molecular compound.

The "butterfly" molecule [Fe3Y(mu 3-O)(2)(CCl3COO)(8)(H2O)(THF)(3)] (in brief {Fe3YO2}) includes three Fe3+ ions which build a robust Fe-3 cluster with a strong intracluster antiferromagnetic exchange and a total spin S = 5/2. It represents the starting magnetic system to study further interactions with magnetic rare earths when Y is replaced with lanthanides. We present heat capacity and equilibrium susceptibility measurements below 2 K, which show that each cluster has a sizeable magnetic anisotropy pointing to the existence of intercluster interactions. However, no phase transition to a long-range magnetically ordered phase is observed down to 20 mK. The intercluster interaction is analysed in the framework of the one-dimensional Blume-Capel model with an antiferromagnetic chain interaction constant J/k(B) = -40(2) mK between Fe-3 cluster spins, and a uniaxial anisotropy with parameter D/k(B) = -0.56(3) K. This is associated to single chains of Fe-3 clusters oriented along the shortest intercluster distances displayed by the crystal structure of {Fe3YO2}. Ac susceptibility measurements reveal that the magnetic relaxation is dominated by a quantum tunnelling process below 0.2 K, and by thermally activated processes above this temperature. The experimental activation energy of this single chain magnet, E-a/k(B) = 3.4(6) K, can be accounted for by the combination of contributions arising from single-molecule magnetic anisotropy and spin-spin correlations along the chains.