4.7 Article

Using N-Heterocyclic Carbenes as Weak Equatorial Ligands to Design Single-Molecule Magnets: Zero-Field Slow Relaxation in Two Octahedral Dysprosium(III) Complexes

Journal

INORGANIC CHEMISTRY
Volume 61, Issue 3, Pages 1264-1269

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.1c03429

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Funding

  1. Russian Science Foundation [17-73-30036-Pi]
  2. Ministry of Science and Higher Education of the Russian Federation
  3. University of Montpellier
  4. CNRS
  5. IUF

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We report the synthesis, structures, and magnetic investigations of two new octahedral dysprosium complexes based on the N-heterocyclic carbene (NHC) tridentate bis(phenoxide) ligand. These complexes exhibit suitable features for slow relaxation of magnetization by utilizing the short Dy-O distances in the axial direction and the weak donor ability of the NHC moiety.
We report the synthesis, structures, and magnetic investigations of two new octahedral dysprosium complexes, based on the original N-heterocyclic carbene (NHC) tridentate bis(phenoxide) ligand, of the respective formulas mer-[DyL(THF)(2)Cl] (1) and mer-[DyL(THF)(3)][BPh4] (2), where L = 1,3-bis(3,5-di-tert-butyl-2-oxidophenyl)-5,5-dimethyl-3,4,5,6-tetrahydropyrimidin-1-ium chloride and THF = tetrahydrofuran. The short Dy-O distances in the axial direction in association with the weak donor ability of the NHC moiety provide a suitable environment for slow relaxation of magnetization, overcoming the previous single-molecule magnets based on NHC ligands.

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