A Trigonal-Pyramidal Erbium(III) Single-Molecule Magnet

Given the recent advent of mononuclear single‐molecule magnets (SMMs), a rational approach based on lanthanides with axially elongated f‐electron charge cloud (prolate) has only recently received attention. We report herein a new SMM, [Li(THF)4[Er{N(SiMe3)2}3Cl]⋅2 THF, which exhibits slow relaxation...

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Published in:Angewandte Chemie International Edition Vol. 54; no. 20; pp. 5864 - 5868
Main Authors: Brown, Andrew J., Pinkowicz, Dawid, Saber, Mohamed R., Dunbar, Kim R.
Format: Journal Article
Language:English
Published: Weinheim WILEY-VCH Verlag 11-05-2015
WILEY‐VCH Verlag
Wiley Subscription Services, Inc
Edition:International ed. in English
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Summary:Given the recent advent of mononuclear single‐molecule magnets (SMMs), a rational approach based on lanthanides with axially elongated f‐electron charge cloud (prolate) has only recently received attention. We report herein a new SMM, [Li(THF)4[Er{N(SiMe3)2}3Cl]⋅2 THF, which exhibits slow relaxation of the magnetization under zero dc field with an effective barrier to the reversal of magnetization (ΔEeff/kB=63.3 K) and magnetic hysteresis up to 3 K at a magnetic field sweep rate of 34.6 Oe s−1. This work questions the theory that oblate or prolate lanthanides must be stabilized with the appropriate ligand framework in order for SMM behavior to be favored. Riding the wave of erbium SMMs: The first trigonal pyramidal mononuclear erbium(III) single‐molecule magnet (SMM) was synthesized and its magnetic properties investigated. Despite containing an axial Cl− ligand, which is expected to reduce the prolate nature of the erbium(III) ion, the molecule exhibits out‐of‐phase signals in the ac susceptibility data in the absence of an external field and hysteresis behavior up to 3 K.
Bibliography:ArticleID:ANIE201411190
This material is based on work supported by the US Department of Energy, Materials Sciences Division, under Grant No. DE-SC0012582. D.P. gratefully acknowledges the financial support of the EC REA within the Marie Curie International Outgoing Fellowship, project MultiCyChem (grant agreement no. PIOF-GA-2011-298569).
EC - No. PIOF-GA-2011-298569
ark:/67375/WNG-CH90X49V-H
istex:C467FBF5F1F6480A3F93500A3AEEFED657A38FE9
US Department of Energy, Materials Sciences Division - No. DE-SC0012582
This material is based on work supported by the US Department of Energy, Materials Sciences Division, under Grant No. DE‐SC0012582. D.P. gratefully acknowledges the financial support of the EC REA within the Marie Curie International Outgoing Fellowship, project MultiCyChem (grant agreement no. PIOF‐GA‐2011‐298569).
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ISSN:1433-7851
1521-3773
DOI:10.1002/anie.201411190