Pushing the limits of magnetic anisotropy in trigonal bipyramidal Ni(ii).
نویسندگان
چکیده
Monometallic complexes based on 3d transition metal ions in certain axial coordination environments can exhibit appreciably enhanced magnetic anisotropy, important for memory applications, due to stabilisation of an unquenched orbital moment. For high-spin trigonal bipyramidal Ni(ii), if competing structural distortions can be minimised, this may result in an axial anisotropy that is at least an order of magnitude stronger than found for orbitally non-degenerate octahedral complexes. Broadband, high-field EPR studies of [Ni(MDABCO)2Cl3]ClO4 (1) confirm an unprecedented axial magnetic anisotropy, which pushes the limits of the familiar spin-only description. Crucially, compared to complexes with multidentate ligands that encapsulate the metal ion, we see only a very small degree of axial symmetry breaking. 1 displays field-induced slow magnetic relaxation, which is rare for monometallic Ni(ii) complexes due to efficient spin-lattice and quantum tunnelling relaxation pathways.
منابع مشابه
Pushing the limits of magnetic anisotropy in trigonal bipyramidal Ni(ii)† †Electronic supplementary information (ESI) available. CCDC 1059709. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c5sc02854j Click here for additional data file. Click here for additional data file.
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ورودعنوان ژورنال:
- Chemical science
دوره 6 12 شماره
صفحات -
تاریخ انتشار 2015