Argentivorous molecules bearing two aromatic side-arms: Ag+-π and CH-π interactions in the solid state and in
Yoichi Habata1, Aya Taniguchi, Mari Ikeda
1Department of Chemistry, Faculty of Science, Toho University, 2-2-1 Miyama, Funabashi, Chiba 274-8510, Japan. habata@chem.sci.toho-u.ac.jp
Abstract:
Seven double-armed cyclens bearing two aromatic side-arms, at the 1- and 7-positions of the cyclens, were prepared via three steps from dimethyl 2,2'-iminodiacetate. The X-ray structures of the Ag(+) complexes and Ag(+)-ion-induced (1)H NMR spectral changes suggest that the two aromatic side-arms cover the Ag(+) ions incorporated in the ligand cavities, as if the aromatic ring "petals" catch the Ag(+) ions in the way a real insectivorous plant (Venus flytrap) catches insects, using two leaves. It is also reported that the CH-π interactions between the aromatic side-arms, as well as the Ag(+)-π interactions, are crucial for double- and tetra-armed cyclens to work as argentivorous molecules.
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