Selective Coordination of Self-Assembled Hexanuclear [Ni4Ln2] and [Ni2Mn2Ln2] (Ln = DyIII, TbIII, and HoIII) Complexes: Stepwise Synthesis, Structures, and Magnetic Properties.

Abstract

The versatility for a unique aggregation of heterometallic 3d-4f and 3d-3d'-4f ions by the new Schiff base ligand 2-{[(2-hydroxy-3-methoxybenzyl)imino]methyl}phenol (H2L) providing O3N donors has been examined. A series of complexes having the general formula [Ln2Ni4(L)4(μ1,3-CH3CO2)2(μ3-OH)4(MeOH)2]·xCH3OH·yH2O [where Ln = DyIII, x = 4, y = 0 (1), Ln = TbIII, x = 0, y = 4 (2), and Ln = HoIII, x = 4, y = 0 (3)] were obtained from the sequential use of lanthanide(III) nitrate salts and Ni(CH3CO2)2·4H2O. The incorporation of two different 3d ions and one 4f ion in the same coordination aggregate was achieved through the isomorphic replacement of two NiII centers by MnIII ions as second group of cationic complexes, [Ln2Ni2Mn2(L)4(μ1,3-CH3CO2)2(μ3-OH)4(MeOH)2](NO3)2·2CH3OH [where Ln = DyIII (4), TbIII (5), and HoIII (6)]. Direct-current (dc) magnetic susceptibility studies hint to the possibility of ferromagnetic interactions occurring in the aggregates, whereas alternating-current susceptibility measurements find both the DyIII analogues, 1 and 4, to show out-of-phase components at zero applied dc field, characteristic of single-molecule-magnet (SMM) behavior. Micro-SQUID studies reveal open hysteresis loops for 1, corroborating its SMM character. Further detailed complete-active-space self-consistent-field and density functional theory calculations were also performed, supporting the experimental findings in complexes 1 and 4.