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Rotaxanes and pseudorotaxanes with Fe-, Pd- and Pt-containing axles. Molecular motion in the solid state and aggregation in solution
Journal article   Peer reviewed

Rotaxanes and pseudorotaxanes with Fe-, Pd- and Pt-containing axles. Molecular motion in the solid state and aggregation in solution

Yuji Suzaki, Toshiaki Taira, Kohtaro Osakada and Masaki Horie
Dalton Transactions, (36), pp.4823-4833
2008

Abstract

This article reviews our recent studies on structure and properties of rotaxanes and pseudorotaxanes with Fe-, Pd- and Pt-containing complexes as the axle component. Electrochemical oxidation of ferrocenylmethylamine in the presence of a hydrogen radical precursor induces formal protonation of the amino group and produces a pseudorotaxane of the resulting ammonium species with a crown ether. Single crystals of the ferrocene-containing pseudorotaxane undergo a thermal crystalline phase transition accompanied by changes in the optical properties of the crystals. X-Ray crystallographic studies of the low- and high-temperature phases revealed different intermolecular interactions and orientations of the aromatic rings in the crystalline state depending on the temperature. End-capping of the ferrocene-containing [2]pseudorotaxane using a cross-metathesis reaction yields [2]rotaxane under mild conditions. A rotaxane having a platinum-carboxylate complex as its axle is converted into related organic and inorganic rotaxanes by partial dissociation of the Pt-O bond. An N-alkylbipyridinium forms [3]pseudorotaxane with α-cyclodextrin (α-CD), and it reacts with platinum and palladium complexes to form the corresponding [5]rotaxanes containing four α-cyclodextrin moieties. Complexes without α-CD components form micelles in aqueous solution, while the addition of α-CD causes degradation of the micelles and the formation of rotaxanes. © 2008 The Royal Society of Chemistry.

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