Coordination-Tuned Single-Molecule-Magnet Behavior of TbIII−CuII Dinuclear Systems

Takashi Kajiwara*, Motohiro Nakano*, Shinya Takaishi and Masahiro Yamashita
Department of Chemistry, Graduate School of Science, Tohoku University, and CREST, Japan Science and Technology Agency (JST), Aramaki, Aoba-ku, Sendai 980-8578, Japan, and Department of Applied Chemistry, Graduate School of Engineering, Osaka University, Suita, Osaka 565-0871, Japan
Inorg. Chem., 2008, 47 (19), pp 8604–8606
DOI: 10.1021/ic8013656
Publication Date (Web): August 29, 2008
Copyright © 2008 American Chemical Society
* To whom correspondence should be addressed. E-mail: kajiwara@agnus.chem.tohoku.ac.jp (T.K.), moto@ch.wani.osaka-u.ac.jp (M.N.).

Tohoku University.

Osaka University.

Abstract

Abstract Image

TbIII−CuII-based single-molecule magnet (SMM) and non-SMM were synthesized to investigate the relationship between magnetic anisotropy and the symmetry of the ligand field by the reaction of [TbCu(o-vanilate)2(NO3)3] with methoxypropylamine (MeOC3H6NH2, 1) or ethoxyethylamine (EtOC2H4NH2, 2). In both complexes, TbIII ions have a bicapped square-antiprism coordination geometry. When the TbIII ion is in a less symmetrical ligand field, it has an easy-axis anisotropy and shows SMM behavior, whereas when it is in a more symmetrical environment, it has an easy-plane anisotropy and exhibits non-SMM behavior.

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History

  • Published In Issue October 06, 2008
  • Article ASAPAugust 29, 2008
  • Received: July 21, 2008

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