| Literature DB >> 27054904 |
Jiang Liu1, Yan-Cong Chen1, Jun-Liang Liu1, Veacheslav Vieru2, Liviu Ungur2,3, Jian-Hua Jia1, Liviu F Chibotaru2, Yanhua Lan4, Wolfgang Wernsdorfer4, Song Gao5, Xiao-Ming Chen1, Ming-Liang Tong1.
Abstract
Single-molecule magnets (SMMs) with a large spin reversal barrier have been recognized to exhibit slow magnetic relaxation that can lead to a magnetic hysteresis loop. Synthesis of highly stable SMMs with both large energy barriers and significantly slow relaxation times is challenging. Here, we report two highly stable and neutral Dy(III) classical coordination compounds with pentagonal bipyramidal local geometry that exhibit SMM behavior. Weak intermolecular interactions in the undiluted single crystals are first observed for mononuclear lanthanide SMMs by micro-SQUID measurements. The investigation of magnetic relaxation reveals the thermally activated quantum tunneling of magnetization through the third excited Kramers doublet, owing to the increased axial magnetic anisotropy and weaker transverse magnetic anisotropy. As a result, pronounced magnetic hysteresis loops up to 14 K are observed, and the effective energy barrier (Ueff = 1025 K) for relaxation of magnetization reached a breakthrough among the SMMs.Entities:
Year: 2016 PMID: 27054904 DOI: 10.1021/jacs.6b02638
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419