Self-Assembly of Coordination Polyhedra with Highly Entangled Faces Induced by Metal-Acetylene Interactions

被引:53
|
作者
Domoto, Yuya [1 ]
Abe, Masahiro [1 ]
Kikuchi, Takashi [2 ]
Fujita, Makoto [1 ]
机构
[1] Univ Tokyo, Sch Engn, Dept Appl Chem, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
[2] Rigaku Corp, 3-9-12 Matsubaracho, Akishima, Tokyo 1968666, Japan
关键词
alkyne ligands; cage compounds; self-assembly; structure elucidation; tripodal ligands; MOLECULAR KNOTS; BINDING;
D O I
10.1002/anie.201913142
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The self-assembly of nanostructures is dominated by a limited number of strong coordination elements. Herein, we show that metal-acetylene pi-coordination of a tripodal ligand (L) with acetylene spacers gave an M3L2 double-propeller motif (M=Cu-I or Ag-I), which dimerized into an M6L4 interlocked cage (M=Cu-I). Higher (M3L2)(n) oligomers were also selectively obtained: an M12L8 truncated tetrahedron (M=Cu-I) and an M18L12 truncated trigonal prism (M=Ag-I), both of which contain the same double-propeller motif. The higher oligomers exhibit multiply entangled facial structures that are classified as a trefoil knot and a Solomon link. The inner cavities of the structures encapsulate counteranions, revealing a potential new strategy towards the synthesis of functional hollow structures that is powered by molecular entanglements.
引用
收藏
页码:3450 / 3454
页数:5
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