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Functionalized [2]Rotaxanes
Author(s) -
Asakawa Masumi,
Ashton Peter R.,
Iqbal Sayeedha,
Quick Andrew,
Stoddart J. Fraser,
Tinker Nigel D.,
White Andrew J.P.,
Williams David J.
Publication year - 1996
Publication title -
israel journal of chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.908
H-Index - 54
eISSN - 1869-5868
pISSN - 0021-2148
DOI - 10.1002/ijch.199600047
Subject(s) - chemistry , supramolecular chemistry , hydroquinone , crystallography , cyclophane , context (archaeology) , rotaxane , crown ether , ring (chemistry) , metal , cryptand , polymer chemistry , stereochemistry , crystal structure , organic chemistry , ion , paleontology , biology
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., toward cyclobis(paraquat‐ p ‐phenylene)) in a supramolecular context is described. The self‐assembly of [2]pseudorotaxanes and [2]rotaxanes, in which cyclobis(paraquat‐ p ‐phenylene) encircles polyether chains intercepted in their middles by a hydroquinone ring and terminated at each end by 12‐crown‐4, 15‐crown‐5, monoaza‐18‐crown‐6, 18‐crown‐6, or adamantyl groups, is achieved using either threading, clipping, or slipping procedures. All the [2]pseudorotaxanes and [2]rotaxanes are characterized 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‐crown‐5 stoppers can be disassembled in solution. The research shows how one kind of complexation can affect another kind of complexation—manifesting itself in a physical change in the system and so acting as a prototype of a potential molecular device.