Role of molecular symmetry in the magnetic relaxation dynamics of five-coordinate Dy(iii) complexes

Abstract

A new family of low-coordinate mononuclear Dy^III single-molecule magnets [(Trapen^TMS)Dy(L^B)] (Trapen = tris(2-aminobenzyl)amine; TMS = SiMe₃; L^B = THF 1, pyridine 2, ONMe₃3) has been synthesized and structurally characterized by single crystal X-ray diffraction. The five-coordinate Dy^III ions exhibit distorted triangular bipyramidal geometries, among the different neutral ligands L^B on the apex and the same Trapen^TMS ligand, making the pyramid base of the trigonal bipyramid. Magnetic data analysis reveals that 1–3 are characteristic of SMM behaviors without a dc field, accompanying an unambiguous quantum tunneling of magnetization. Under an extra dc field of 500 Oe, field-induced slow magnetic relaxation behaviors occur with Raman and/or QTM processes. Ab initio calculations were also performed to rationalize the observed discrepancy in the magnetic behaviors, and the result illustrates that the SMM behavior could be effectively manipulated by the axial symmetry of the triangular bipyramidal Dy^III motifs.