期刊
CHEMICAL SCIENCE
卷 9, 期 31, 页码 6564-6571出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7sc04482h
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资金
- National Science Foundation [CHE-1058889, CHE-1363274]
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [1363274] Funding Source: National Science Foundation
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, [NixCo1 (-x)(cyclam)(NO3)(2)](NO3)center dot 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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