Constitutionally Asymmetric and Chiral [2]Pseudorotaxanes1

The self-assembly and characterization of a range of chiral pseudorotaxanes has been explored using chiroptical methods. The syntheses of (i) constitutionally asymmetric acyclic hydroquinone-containing polyethers and (ii) optically active hydroquinone-containing acyclic polyethers, bearing pairs of methyl or isobutyl groups related to each other in a C 2 -symmetric manner within the polyether backbone, are described. The combination of (i) the tetracationic cyclophane cyclobis(paraquat- p -phenylene) tetrakis(hexafluorophosphate), possessing a π-electron deficient cavity, and (ii) the linear noncentrosymmetric acyclic polyethers produces [2]pseudorotaxanes that have been characterized by 1 H NMR, UV/vis and circular dichroism (CD) spectroscopies in solution and by X-ray crystallography in the solid state. The introduction of constitutional asymmetry or chirality gives rise to a number of different geometries for the [2]pseudorotaxanes in both the solution and solid states. In particular, CD-spectroscopic measurements on the optically active [2]pseudorotaxanes have shown that depending on the positions of the C 2 symmetrically related chiral centers in the polyether chains with respect to the hydroquinone rings the chirality present in the π-electron rich threadlike guest can induce chirality that is associated with the supramolecular structure as a whole, resulting in a chiral charge-transfer transition involving not only the π-donors in the chiral guests but also the π-acceptors in the achiral host.