4.7 Article

Insertion of single-ion magnets based on mononuclear Co(II) complexes into ferromagnetic oxalate-based networks

Journal

DALTON TRANSACTIONS
Volume 50, Issue 17, Pages 5931-5942

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d1dt00595b

Keywords

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Funding

  1. EU [MOL-2D 788222, FET-OPEN COSMICS 766726]
  2. Spanish MCIU [MAT-2017-89993-R, CEX2019-000919-M]
  3. Generalitat Valenciana [iDiFEDER/2018/061]
  4. Ministry of Education and Science of Russian Federation [14.W03.31.0001]
  5. Generalitat Valenciana (PROMETEO program)

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The 1:2 and 1:1 Co(II) complexes of the L ligand have been synthesized and characterized for their structural and magnetic properties, showing octahedral high-spin Co(II) and field-induced slow relaxation of magnetization; one of the compounds has been incorporated into a bimetallic oxalate-based network leading to a novel 3D compound with ferromagnetic ordering, with EPR measurements suggesting weak magnetic coupling between the two sublattices.
The 1:2 and 1:1 Co(II) complexes of the L ligand (L = 6-(3,5-diamino-2,4,6-triazinyl)2,2'-bipyridine) with formulas [Co-II(L)(2)](ClO4)(2)center dot 0.5MeCN center dot Et2O (1) and [Co-II(L)(CH3CN)(2)(H2O)](ClO4)(2)center dot MeCN (2) have been prepared. The structural and magnetic characterization of the two compounds shows that they contain octahedral high-spin Co(II) and present a field-induced slow relaxation of the magnetization. 1 has been inserted into a bimetallic oxalate-based network leading to a novel achiral 3D compound of formula [Co-II(L)(2)][(MnCrIII)-Cr-II(ox)(3)](2)center dot(solvate) (3) exhibiting ferromagnetic ordering below 4.6 K. EPR measurements suggest a weak magnetic coupling between the two sublattices.

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