Supramolecular Entanglement from Interlocked Molecular Nanomagnets

被引:37
|
作者
Stoumpos, Constantinos C. [2 ]
Inglis, Ross [3 ]
Karotsis, Georgios [3 ]
Jones, Leigh F. [3 ]
Collins, Anna [3 ]
Parsons, Simon [3 ]
Milios, Constantinos J. [3 ,4 ]
Papaefstathiou, Giannis S. [1 ]
Brechin, Euan K. [3 ]
机构
[1] Univ Athens, Dept Chem, Inorgan Chem Lab, Panepistimiopolis 15771, Zogragfou, Greece
[2] Univ Patras, Dept Chem, Patras 36004, Greece
[3] Univ Edinburgh, Sch Chem, Edinburgh EH9 3JJ, Midlothian, Scotland
[4] Univ Crete, Dept Chem, Voutes 71003, Herakleion Cret, Greece
基金
英国工程与自然科学研究理事会;
关键词
TARGETED STRUCTURAL DISTORTION; INORGANIC 3D NETWORKS; COORDINATION POLYMERS; SOLID-STATE; CHEMISTRY; MAGNETS; COMPLEX; DESIGN; MAGNETIZATION; REACTIVITY;
D O I
10.1021/cg800947z
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The trinuclear nanomagnet [(Mn3O)-O-III(Et-sao)(3)(MeOH)(3)](ClO4) (1) has been utilized as a building block for the construction of the hexanuclear cluster [((Mn3O)-O-III(Et-saO)(3)(O2CPh)(EtOH)}(2)(4,4'-bpe}(2)] (3) that conforms to a rectangle and the two-dimensional coordination polymer { [(Mn3O)-O-III(sao)(3)(4,4'-bpe)(1.5)]ClO4 center dot 3MeOH)(n) (2 center dot 3MeOH). The latter exhibits an unprecedented type of entanglement that is based on host guest interactions. The polygon versus the polymer is rationalized in terms of changing an auxiliary anion that influences the arrangement of the potentially "vacant" coordination axes on each Mn-III ion of the trinuclear precursor and thereby directing the self-assembly process.
引用
收藏
页码:24 / 27
页数:4
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