Rational Improvement of Single-Molecule Magnets by Enforcing Ferromagnetic Interactions

The anisotropy barrier of polynuclear single-molecule magnets is expected to be higher with less tunneling the better stabilized the spin ground state is so that less M_S mixing in the ground state and with excited spin states occur. We have realized this experimentally in two structurally related heptanuclear SMMs: the triplesalen-based Mn^III ₆ Cr^III]³⁺ and the triplesalalen-based *Mn^III ₆ Cr^III]³⁺ . The ligand system triplesalen was developed to enforce ferromagnetic interactions by the spin-polarization mechanism. However, we found weak antiferromagnetic couplings, that we assigned to an inefficient spin-polarization by a heteroradialene formation. To prevent this heteroradialene formation, the triplesalalen ligand H₆talalen was designed. Here, we present the building block (talalen )Mn^III₃]³⁺ and its application for the assembly of {(talalen )Mn^III₃}₂{Cr^III(CN)₆}]³⁺ (= *Mn^III ₆ Cr^III]³⁺ ). Both the trinuclear and heptanuclear complexes are SMMs. The comparison to the related triplesalen complex (feld )Mn^III₃]³⁺ proves the absence of heteroradialene character and the enforcement of ferromagnetic Mn^III-Mn^III interactions in the (talalen )^6? complexes. This results in an increase of the barrier for spin reversal U_eff from 25 K in the triplesalen-based Mn^III ₆ Cr^III]³⁺ SMMs to 37 K in the triplesalalen-based *Mn^III ₆ Cr^III]³⁺ SMM proving the success of our concept. Based on this study, the next step in the rational improvement of our SMMs is discussed.