The mononuclear oxazolidine nitroxide complex [Mn II(L)2](ClO4)2 (1) (L ,4-dimethyl-2,2-di(2-pyridyl)oxazolidine N-oxide) has been synthesized and investigated using single-crystal X-ray diffraction, variable-temperature magnetic susceptibility measurements, and electrochemistry. The structural analysis reveals bond lengths compatible with a linear L –MnII–L arrangement where the ligands are in the neutral ligand form and the central MnII ion is high spin (S = 5/2). Although analysis of the variable-temperature magnetic susceptibility data suggests a strong antiferromagnetic metal– radical interaction, the radical–radical intramolecular interaction could not be determined unambiguously from such fits. The resultant isolated S = 3/2 ground state is confirmed by low-temperature magnetization versus field measurements. Electrochemical studies reveal similar square schemes and redox intermediates to the previously reported analogues [FeII(L)2][BF4]2 and [CoII(L )2][NO3]2.
|Number of pages||7|
|Journal||Australian Journal of Chemistry|
|Publication status||Published - 15 Sep 2014|
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- School of Applied Sciences - Senior Lecturer
- Centre for Stress and Age-Related Disease
- Chemistry Research and Enterprise Group