Effect of Axial Ligands on Easy-Axis Anisotropy and Field-Induced Slow Magnetic Relaxation in Heptacoordinated FeII Complexes

Arpan Mondal, Shu Qi Wu, Osamu Sato, Sanjit Konar

研究成果: Contribution to journalArticle査読

5 被引用数 (Scopus)

抄録

A rational approach to modulating easy-axis magnetic anisotropy by varying the axial donor ligand in heptacoordinated FeII complexes has been explored. In this series of complexes with formulae of [Fe(H4L)(NCS)2]⋅3 DMF⋅0.5 H2O (1), [Fe(H4L)(NCSe)2]⋅3 DMF⋅0.5 H2O (2), and [Fe(H4L)(NCNCN)2]⋅DMF⋅H2O (3) [H4L=2,2′-{pyridine-2,6-diylbis(ethan-1-yl-1-ylidene)}bis(N-phenylhydrazinecarboxamide)], the axial positions are successively occupied by different nitrogen-based π-donor ligands. Detailed dc and ac magnetic susceptibility measurements reveal the existence of easy-axis magnetic anisotropy for all of the complexes, with 1 [Ueff=21 K, τ0=1.72×10−6 s] and 2 [Ueff=25 K, τ0=2.25×10−6 s] showing field-induced slow magnetic relaxation behavior. However, both experimental studies and theoretical calculations indicate the magnitude of the D value of complex 3 to be larger than those of complexes 1 and 2 due to the axial bond angle being smaller than that for an ideal geometry. Detailed analysis of the field and temperature dependences of relaxation time for 1 and 2 has revealed that multiple relaxation processes (quantum tunneling of magnetization, direct, and Raman) are involved in slow magnetic relaxation for both of these complexes. Magnetic dilution experiments support the role of intermolecular short contacts.

本文言語英語
ページ(範囲)4780-4789
ページ数10
ジャーナルChemistry - A European Journal
26
21
DOI
出版ステータス出版済み - 4 9 2020

All Science Journal Classification (ASJC) codes

  • Catalysis
  • Organic Chemistry

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