Issue 37, 2019

Slow magnetic relaxation in Ni–Ln (Ln = Ce, Gd, Dy) dinuclear complexes

Abstract

Three new isomorphous complexes [Ni(o-van-en)LnCl3(H2O)] [H2(o-van-en) = N,N′-ethylene-bis(3-methoxysalicylaldiminate; Ln = Ce (1), Gd (2), Dy (3)] were prepared by a stepwise reaction using mild conditions and were structurally characterised as dinuclear molecules in which Ni and Ln are coordinated by the compartmental Schiff base ligand (o-van-en)= and doubly bridged by O atoms. While the nickel(II) centre is diamagnetic within the N2O2 square-planar coordination of the Schiff base ligand, the lanthanide atoms are octa-coordinated to give an {LnCl3O5} chromophore with a fac-arrangement of the chlorido ligands. AC magnetic measurements revealed that all three complexes, including the nominally isotropic Gd(III) system, show field induced slow magnetic relaxation with two or three relaxation channels: at T = 1.9 K the low-frequency relaxation time is τLF(1) = 0.060 s at BDC = 0.5 T, τLF(2) = 0.37 s at BDC = 0.3 T, and τLF(3) = 1.29 s at BDC = 0.15 T.

Graphical abstract: Slow magnetic relaxation in Ni–Ln (Ln = Ce, Gd, Dy) dinuclear complexes

Supplementary files

Article information

Article type
Paper
Submitted
20 May 2019
Accepted
17 Aug 2019
First published
23 Aug 2019
This article is Open Access
Creative Commons BY-NC license

Dalton Trans., 2019,48, 13943-13952

Slow magnetic relaxation in Ni–Ln (Ln = Ce, Gd, Dy) dinuclear complexes

A. Vráblová, M. Tomás, L. R. Falvello, Ľ. Dlháň, J. Titiš, J. Černák and R. Boča, Dalton Trans., 2019, 48, 13943 DOI: 10.1039/C9DT02122A

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