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Título

Order in disorder: solution and solid-state studies of [MIII 2 MII 5] wheels (MIII = Cr, Al; MII = Ni, Zn)

AutorFraser, Hector W. L.; Nichol, Gary S.; Uhrín, Dušan; Gro Nielsen, Ulla; Evangelisti, Marco CSIC ORCID ; Schnack, Jürgen; Brechin, Euan K.
Fecha de publicación2018
EditorRoyal Society of Chemistry (UK)
CitaciónDalton Transactions 47(34): 11834-11842 (2018)
ResumenA family of heterometallic Anderson-type ‘wheels’ of general formula [MIII2MII5(hmp)12](ClO4)4 (where MIII = Cr or Al and MII = Ni or Zn giving [Cr2Ni5] (1), [Cr2Zn5] (2), [Al2Ni5] (3) and [Al2Zn5] (4); hmpH = 2-pyridinemethanol) have been synthesised solvothermally. The metallic skeleton common to all structures describes a centred hexagon with the MIII sites disordered around the outer wheel. The structural disorder has been characterised via single crystal X-ray crystallography, 1–3D 1H and 13C solution-state NMR spectroscopy of the diamagnetic analogue (4), and solid-state 27Al MAS NMR spectroscopy of compounds (3) and (4). Alongside ESI mass spectrometry, these techniques show that structure is retained in solution, and that the disorder is present in both the solution and solid-state. Solid-state dc susceptibility and magnetisation measurements on (2) and (3) reveal the Cr–Cr and Ni–Ni exchange interactions to be JCr–Cr = −1 cm−1 and JNi–Ni,r = −5 cm−1, JNi–Ni,c = 10 cm−1. Fixing these values allows us to extract JCr–Ni,r = −1.2 cm−1, JCr–Ni,c = 2.6 cm−1 for (1), the exchange between adjacent Ni and Cr ions on the ring is antiferromagnetic and between Cr ions on the ring and the central Ni ion is ferromagnetic.
Versión del editorhttps://doi.org/10.1039/C8DT00685G
URIhttp://hdl.handle.net/10261/181217
DOI10.1039/C8DT00685G
ISSN1477-9226
E-ISSN1477-9234
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