FUNCTIONALIZED [2]ROTAXANES

Citation
M. Asakawa et al., FUNCTIONALIZED [2]ROTAXANES, Israel Journal of Chemistry, 36(4), 1996, pp. 329-340
Citations number
63
Categorie Soggetti
Chemistry
Journal title
ISSN journal
00212148
Volume
36
Issue
4
Year of publication
1996
Pages
329 - 340
Database
ISI
SICI code
0021-2148(1996)36:4<329:F[>2.0.ZU;2-0
Abstract
The synthesis of a series of dumbbell-shaped compounds, which can act as a host (e.g., toward alkali metal cations) and as a guest (e.g., to ward cyclobis(paraquat-p-phenylene)) in a supramolecular context is de scribed. The self-assembly of [2]pseudorotaxanes and [2]rotaxanes, in which cyclobis(paraquat-p-phenylene) encircles polyether chains interc epted in their middles by a hydroquinone ring and terminated at each e nd by 12-crown-4, 15-crown-5, monoaza-18-crown-6, 18-crown-6, or adama ntyl groups, is achieved using either threading, clipping, or slipping procedures. All the [2]pseudorotaxanes and [2]rotaxanes are character ized in solution by spectroscopic means and, in the case of two of the [2]rotaxanes, by X-ray crystal structures in the solid state. In the presence of metal ions, [2]pseudorotaxanes carrying 12-crown-4 or 15-c rown-5 stoppers can be disassembled in solution. The research shows ho w one kind of complexation can affect another kind of complexation-man ifesting itself in a physical change in the system and so acting as a prototype of a potential molecular device.