A {CoIII2DyIII4} Single-Molecule Magnet with an Expanded Core Structure
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STATI, Dumitru, VAN LEUSEN, Jan, NAUSHAD, Ahmed, KRAVTSOV, Victor, KOGERLER, Paul, BACA, Svetlana. A {CoIII2DyIII4} Single-Molecule Magnet with an Expanded Core Structure. In: Crystal Growth and Design, 2023, vol. 23, pp. 395-402. ISSN 1528-7483. DOI: https://doi.org/10.1021/acs.cgd.2c01085
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Crystal Growth and Design
Volumul 23 / 2023 / ISSN 1528-7483

A {CoIII2DyIII4} Single-Molecule Magnet with an Expanded Core Structure

DOI:https://doi.org/10.1021/acs.cgd.2c01085

Pag. 395-402

Stati Dumitru1, Van Leusen Jan2, Naushad Ahmed3, Kravtsov Victor1, Kogerler Paul2, Baca Svetlana1
 
1 Institute of Applied Physics,
2 Institute of Inorganic Chemistry RWTH Aachen University,
3 Indian Institute of Technology Hyderabad, Kandi
 
 
Disponibil în IBN: 31 ianuarie 2023


Rezumat

The coordination cluster compound [CoIII2DyIII4(OH)2(ib)8(bdea)2(NO3)4(H2O)2]·2MeCN (1) self-assembles in a high-yield reaction of cobalt(II) isobutyrate (ib) with Dy(NO3)3·6H2O and N-butyldiethanolamine (H2bdea) in air. The Ci-symmetric {CoIII2DyIII4} core fragment features two {CoDy23-OH)} triangles, joined by one of their Dy sites via μ-O and μ-carboxylate bridges. This results in a flat zigzag metal skeleton, in contrast to previously reported hexanuclear {Co2Ln43-OH)2} clusters, namely, exhibiting a more condensed combination of two {CoLn23-OH)} triangles that form a Dy4 rhombus. According to ac susceptibility measurements, this rearrangement in 1 reduces quantum tunneling of the magnetization and hence pushes up the onset of pronounced out-of-phase signals at zero bias field to 14 K, a significant change vs the more condensed {Co2Dy4} structures. As intermolecular interactions between coordination clusters in the solid state are well-known to also influence SMM features, comparative Hirshfeld surface analyses are also presented.

Cuvinte-cheie
Carboxylation, Cobalt compounds, Coordination reactions, magnetic susceptibility