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Slow magnetic relaxation in octahedral low-spin Ni(iii) complexes
Herein we report the first examples of single-molecule magnet (SMM) behaviour in S = 1/2 Ni(iii) complexes. We find that low-spin 3d(7)trans-[Ni(III)(cyclam)(X)(2)]Y complexes (cyclam = 1,4,8,11-tetraazacyclotetradecane; X and Y are singly charged anions) exhibit field-induced slow relaxation of mag...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6115677/ https://www.ncbi.nlm.nih.gov/pubmed/30310588 http://dx.doi.org/10.1039/c7sc04482h |
Sumario: | Herein we report the first examples of single-molecule magnet (SMM) behaviour in S = 1/2 Ni(iii) complexes. We find that low-spin 3d(7)trans-[Ni(III)(cyclam)(X)(2)]Y complexes (cyclam = 1,4,8,11-tetraazacyclotetradecane; X and Y are singly charged anions) exhibit field-induced slow relaxation of magnetization for O-donor axial ligands (nitrate) but not for N-donor variants (isothiocyanate). Experimental and electronic structure computational investigations indicate that intrinsic spin polarisation of low-spin Ni(iii) is modulated significantly by local coordination geometry and supramolecular interactions. Solid state dilution of Ni(iii) with diamagnetic Co(iii) ions forms a related complex salt, [Ni(x)Co(1–x)(cyclam)(NO(3))(2)](NO(3))·2HNO(3) (0.1 < x < 1), which preserves slow magnetic dynamics, thus supporting a molecular component to slow relaxation. An initial analysis of magnetic relaxation lifetime fits best to a combination of Raman and direct relaxation processes. |
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