Abstract

We hereby report a dinuclear Dy(iii) complex, [Dy(LH3)Cl2]2·2Et2O (1) (LH4 = 2,3-dihydroxybenzylidene)-2-(hydroxyimino)propanehydrazide where both the metal centres are in a pentagonal bipyramidal (PBP) geometry with the axial positions being occupied by negatively charged Cl- ions. The complex as well as it's 10% diluted analogue (110) do not show zero-field SMM behaviour. However, in the presence of small optimum dc fields the slow relaxation of magnetization was displayed. The effective energy barrier for 110 at 800 Oe of applied field was extracted as 83(17) K with τ0 = 2(4) × 10-12 s. Through a combined experimental and ab initio electronic structure calculations studies we have thoroughly analysed the role of the ligand field around the Dy(iii), present in pentagonal bipyramidal geometry, in contributing to the slow relaxation of magnetization.

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