4.7 Article

A mononuclear Ni(II) complex: a field induced single-molecule magnet showing two slow relaxation processes

Journal

DALTON TRANSACTIONS
Volume 44, Issue 28, Pages 12484-12487

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c5dt01213a

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Funding

  1. [VEGA 1/0233/12]
  2. [VEGA 1/0522/14]
  3. [APVV-0014-11]

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The mononuclear complex [Ni(pydc)(pydm)]center dot H2O, pyridine-2,6-dicarboxylato-2,6-bis(hydroxymethyl) pyridine nickel(II) monohydrate, features a highly axially compressed pseudo-octahedral chromophore with significant rhombic contribution that is responsible for the sizable magnetic anisotropy of the Ni(II) ion, D/hc approximate to -14 cm(-1). This complex displays superparamagnetic behaviour in an applied external field that culminates at B-DC = 0.2 T. Two relaxation processes are evidenced; the faster can be analyzed in terms of the Orbach, direct, and Raman processes yielding U/k(B) = 21.2 (+/- 1.3) K and tau(0) = 3.83 (+/- 1.21) x 10(-7) s. This is the first example of a field-induced single-molecule magnet in the class of hexacoordinate Ni(II) complexes.

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