Towards Understanding Prolate 4$f$ Monomers: Numerical Predictions and Experimental Validation of Electronic Properties and Slow Relaxation in a Muffin-shaped Er$^\mathrm{III}$ Complex

TL;DR

This study combines synthesis, structural analysis, and advanced spectroscopy to understand the electronic properties and slow magnetic relaxation in a novel Er(III) complex with potential implications for single-molecule magnet research.

Contribution

It provides the first detailed experimental and theoretical characterization of the electronic structure and magnetic relaxation pathways in a prolate 4f monomer with a muffin-shaped geometry.

Findings

Complex exhibits field-induced slow magnetic relaxation.

Experimental EPR determines g-factors and zero field splittings.

Theoretical calculations agree with experimental data.

Abstract

We report the synthesis, crystal structure and magnetic properties of the triply-capped, slightly distorted trigonal-prismatic complex [Er(PPTMP)$_2$(H$_2$O)][OTf]$_3$ (PPTMP = (4-(6-(1,10-phenanthrolin-2-yl)pyridin-2-yl)-1H-1,2,3-triazol-1-yl)methyl pivalate) ($\mathbf{1}$). Complex $\mathbf{1}$ is shown to exhibit field-induced slow relaxation of the magnetisation at $B = 0.1\,\mathrm{T}$ via two distinct relaxation paths. Using tunable high-frequency/high-field electron paramagnetic resonance spectroscopy, we experimentally determine the effective $g$-factors and zero field splittings of the two energetically lowest Kramers doublets (KD). Our data reveal that the triply-capped, slightly distorted trigonal-prismatic ligand field favours an $m \simeq \pm 9/2$ magnetic ground state, while the main contribution to the first excited KD at $\Delta_{1 \rightarrow 2} = 780(5)\,\mathrm{GHz}$ is suggested to be $m \simeq \pm 5/2$. The ground state $g$-tensor has generally axial form but hosts significant transversal components, which we conclude to be the source of SMM-silent behaviour in zero field. Our findings are backed up by ab-initio spin-orbit configuration interaction calculations showing excellent agreement with the experimental data.