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.