کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1303721 | 1498945 | 2014 | 4 صفحه PDF | دانلود رایگان |
• New supertetrahedral manganese complexes.
• Mixed-valent [MnII4MnIII6] decanuclear clusters.
• Spin-ground state S = 12 ± 1.
Two manganese complexes, [MnII4MnIII6Cl4(CH3OCH2CH2O)12 O4][MnII3TiIVCl6(CH3OCH2CH2O)6] (1) and [MnII4MnIII6Cl4(CH3OCH2CH2O)12O4] [Mn4II Cl10(CH3OCH2CH2OH)4]∙0.5CH3OCH2CH2OH, (2) have been obtained and characterized by single-crystal X-ray diffraction. Both structures consist of the decametallic dicationic [MnII4MnIII6Cl4(CH3OCH2CH2O)12O4]2 + core constructed by four vertex-sharing [MnIII3MnIIO]9 + tetrahedra. Also, these compounds contain the different tetrametallic dianions: [MnII3TiIVCl6(CH3OCH2CH2O)6]2 − (in complex 1) and [Mn4IICl10(CH3OCH2CH2OH)4]2 − (in complex 2). Magnetic dc and ac susceptibility measurements for compound (1) show that the dicationic decanuclear magnetic cluster possesses an S = 12 ± 1 spin ground-state.
Two isostructural decanuclear mixed-valent manganese complexes with “supertetrahedral” topology have been obtained and characterized by single-crystal X-ray diffraction. Magnetic studies reveal an S = 12 ± 1 ground-state for the decametallic core.Figure optionsDownload as PowerPoint slide
Journal: Inorganic Chemistry Communications - Volume 45, July 2014, Pages 71–74