Approaches to Molecular Magnetic Materials from the Use of Cyanate Groups in Higher Oxidation State Metal Cluster Chemistry: Mn14 and Mn16

被引:16
作者
Alexandropoulos, Dimitris I. [1 ]
Papatriantafyllopoulou, Constantina [2 ]
Li, Chaoran [2 ]
Cunha-Silva, Luis [3 ,4 ]
Manos, Manolis J. [5 ]
Tasiopoulos, Anastasios J. [6 ]
Wernsdorfer, Wolfgang [7 ]
Christou, George [2 ]
Stamatatos, Theocharis C. [1 ]
机构
[1] Brock Univ, Dept Chem, St Catharines, ON L2S 3A1, Canada
[2] Univ Florida, Dept Chem, Gainesville, FL 32611 USA
[3] Univ Porto, Fac Sci, REQUIMTE, P-4169007 Oporto, Portugal
[4] Univ Porto, Fac Sci, Dept Chem & Biochem, P-4169007 Oporto, Portugal
[5] Univ Ioannina, Dept Chem, GR-45110 Ioannina, Greece
[6] Univ Cyprus, Dept Chem, CY-1678 Nicosia, Cyprus
[7] CNRS, Inst Neel, Nanosci Dept, F-380412 Grenoble 9, France
基金
美国国家科学基金会;
关键词
Cluster compounds; Cyanates; Manganese; N; O ligands; Single-molecule magnets; HIGH-NUCLEARITY; SPIN-STATE; SINGLE; COMPLEXES; LIGANDS; CRYSTAL; AZIDE; MN-17;
D O I
10.1002/ejic.201300099
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The initial employment of cyanato groups in higher oxidation state manganese cluster chemistry, in conjunction with the gem-diolate form of di-2-pyridylketone or 2,6-diacetylpyridine dioxime chelate ligands, has afforded structurally interesting MnII/III14 and MnII/III/IV16 clusters, respectively. In both complexes, the end-on bridging cyanato groups show an obvious preference in binding through their O atom, a significantly different ligation than that for the homoatomic-type N3 ligand. The Mn14 compound shows entirely visible out-of-phase signals below 5 K and large hysteresis loops below 2 K.
引用
收藏
页码:2286 / 2290
页数:5
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