ABSTRACT
Two Mn(4) single-molecule-magnet (SMM)-based coordination polymers, {[Mn(4)O(salox)(3)(N(3))(3)(DMF)(2)(H(2)O)(dpp)]·0.5MeOH}(n) (1·0.5MeOH; H(2)salox = salicylaldoxime; dpp = 1,3-di-4-pyridylpropane; DMF = N,N-dimethylformamide) and {[Mn(4)O(Me-salox)(3)(N(3))(3)(dpp)(1.5)]·1.5Et(2)O}(n) (2·1.5Et(2)O; Me-H(2)salox = hydroxyphenylethanone oxime), are self-assembled from Mn(ClO(4))(2)·6H(2)O/H(2)salox and Mn(ClO(4))(2)·6H(2)O/Me-H(2)salox systems with dpp and NaN(3) in DMF/MeOH, respectively. Both compounds comprise a mixed-valence tetranuclear manganese core, [Mn(II)Mn(III)(3)O](9+), which serves as a building unit for subsequent assembly via oximate and azido ligands. The flexible dpp ligand links with a Mn(4) unit, leading to the formation of a one-dimensional helical structure in 1·0.5MeOH and a three-dimensional pcu network in 2·1.5Et(2)O. The magnetic data analysis shows that antiferromagnetic interactions within the Mn(4) units resulted in S = (3)/(2) and (7)/(2) ground states for 1·0.5MeOH and 2·1.5Et(2)O, respectively. Both compounds show SMM behavior, as evidenced by frequency-dependent out-of-phase signals in alternating-current magnetic susceptibility and magnetic hysteresis loop studies with an energy barrier of U(eff) = 37 K for 2·1.5Et(2)O.
