A centrosymmetric dinuclear complex, [Dy
2(H
2dapp)
2(
μ-OH)
2(H
2O)
2]·4TCNQ·2CH
3OH, was synthesized using the TCNQ
·− radical anion (TCNQ = 7,7,8,8-tetracyanoquino-dimethane) and pentadentate nitrogen-containing Schiff base ligand (H
2dapp = 2,6-diacetylpyridine)-bis(2-pyridylhydrazone).
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A centrosymmetric dinuclear complex, [Dy
2(H
2dapp)
2(
μ-OH)
2(H
2O)
2]·4TCNQ·2CH
3OH, was synthesized using the TCNQ
·− radical anion (TCNQ = 7,7,8,8-tetracyanoquino-dimethane) and pentadentate nitrogen-containing Schiff base ligand (H
2dapp = 2,6-diacetylpyridine)-bis(2-pyridylhydrazone). In the Dy
2 dimer, the two Dy
III ions adopt eight-coordinated geometries intermediate between
D4d and
D2d symmetries, linked by two OH
− groups, with ferromagnetic Dy-Dy interactions. The TCNQ
·− radical anions are uncoordinated, and they pack tightly into antiparamagnetic dimers to balance the system charge. Under zero field, weak magnetic relaxation was observed, with an approximate
Δeff = 2.82 K and
τ0 = 6.88 × 10
−6 s. This might be attributed to the short intermolecular Dy···Dy distance of 7.97 Å, which could enhance intermolecular dipolar interactions and quantum tunneling of magnetization (QTM).
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