کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1302531 | 974698 | 2011 | 4 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: A novel tetranuclear MnII2MnIII2 cluster [Mn4(hmp)6(N3)4]: Synthesis, crystal structure and magnetic properties A novel tetranuclear MnII2MnIII2 cluster [Mn4(hmp)6(N3)4]: Synthesis, crystal structure and magnetic properties](/preview/png/1302531.png)
A novel tetranuclear mixed-valence manganese(II/III) cluster [Mn4(hmp)6(N3)4] (1) where hmp is the anion of 2-hydroxymethylpyridine, was obtained by the reaction of manganese perchlorate with hmpH and NaN3 in acetonitrile. Complex 1 was characterized by chemical analysis, IR spectroscopy, single crystal X-ray diffraction and variable-temperature magnetic susceptibility studies. Complex 1 crystallizes in triclinic system with space group Pī consisting of mixed-valence Mn ions whose coordination geometry can be described as distorted octahedron. The magnetic properties were studied in the temperature range of 1.9–300 K and the results show that mixed-valence Mn ions are ferromagnetically coupled in the cluster leading to an S = 9 ground state.
A mixed-valence manganese(II/III) cluster [Mn4(hmp)6(N3)4] (hmp is the anion of 2-hydroxymethylpyridine) (1) was synthesized by reaction of manganese perchlorate with hmpH and NaN3 in acetonitrile. Single crystal X-ray diffraction showed each Mn ion owns a distorted octahedral coordination geometry. The magnetic studies indicate that Mn ions are ferromagnetically coupled in the cluster leading to an S = 9 ground state.Figure optionsDownload as PowerPoint slideResearch highlight
► A mixed-valence Mn4 cluster [Mn4(hmp)6(N3)4] (1) has been synthesized.
► Single crystal X-ray diffraction showed each Mn ion owns a distorted octahedral coordination geometry.
► The magnetic studies indicated that Mn ions are ferromagnetically coupled.
► Complex 1 can be employed as a building block forming extended metal complexes.
Journal: Inorganic Chemistry Communications - Volume 14, Issue 9, September 2011, Pages 1329–1332