Synthesis, structures and magnetic studies of hexanuclear lanthanide complexes: SMM behavior of the Dy III analogue and MCE properties of the Gd III analogue.

The synthesis, structure and magnetic properties of homometallic hexanuclear lanthanide complexes [Ln 6 (HL) 4 (tfa) 4 (S) 2 ]·2NO 3 · x H 2 O· y MeOH (1, Ln = Gd, S = MeOH, x = 0, y = 0; 2, Ln = Tb, S = H 2 O, x = 2, y = 2; 3, Ln = Dy, S = MeOH, x = 0, y = 2; 4, Ln = Er, S = MeOH, x = 0, y = 2). [(H 4 L) = 6-((bis(2-hydroxyethyl)amino)- N '-(2-hydroxybenzylidene)picolinohydrazide) (tfa = trifloroacetylacetone)] are reported. These hexanuclear assemblies are made up of two trinuclear triangular sub-units linked through the oxygen atoms of two phenoxide bridging groups in a corner sharing arrangement. Magnetic studies reveal that 1 displays a magnetocaloric effect with a maximum value of -Δ S m = 21.03 J kg -1 K -1 at T = 3 K and under an applied field change Δ B = 5 T. Complex 3 shows slow relaxation of magnetization even under zero applied field although a clear maximum in the ac susceptibility plots cannot be seen. However, under an optimal applied field of 0.2 T, clear maxima are observed in the out-of-phase ( χ '' M ) component of the ac susceptibility in the temperature range 3.5 K (2 kHz) to 10.5 K (10 kHz). The temperature dependence of the relaxation times could be fitted to the sum of Orbach, Raman and QTM relaxation processes affording the following parameters: τ o = 3.4(9) × 10 -8 s, U eff = 94(2) K, B Raman = 16.43(1) K - n s -1 , n = 3.2(3) and τ QTM = 0.0044(3) s. 4, under an applied magnetic field of 0.2 T, shows slow relaxation of magnetization through a thermally activated Orbach process with U eff = 18.2(9) K and τ o = 3.5(3) × 10 -8 s.