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Breaking the Magic Border of One Second for Slow Magnetic Relaxation of Cobalt-Based Single Ion Magnets.

Roman BočaCyril RajnákJán MoncolJán TitišDušan Valigura
Published in: Inorganic chemistry (2018)
Instead of assembling complex clusters and/or expensive lanthanide-based systems as single ion magnets, we are focusing on mononuclear cobalt(II) systems among which the complex under study, [Co( pydca)( dmpy)]2·H2O (1), shows a field supported slow magnetic relaxation on the order of seconds at low temperature ( pydca = pyridine-2,6-dicarboxylato, dmpy = 2,6-dimethanolpyridine). The low-frequency relaxation time is as slow as τ(LF) = 1.35(6) s at T = 1.9 K and BDC = 0.4 T. The properties of 1 are compared to the previously reported nickel and copper analogues which were the first examples of single ion magnets in the family of Ni(II) and Cu(II) complexes.
Keyphrases
  • metal organic framework
  • single molecule
  • reduced graphene oxide
  • molecularly imprinted
  • carbon nanotubes
  • mass spectrometry
  • oxide nanoparticles
  • solid state
  • structure activity relationship