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Taylor and Francis Group, Supramolecular Chemistry, 1-2(23), p. 42-52, 2010

DOI: 10.1080/10610278.2010.510189

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Bigger, Better, Faster: Molecular Shuttles with Sterically Non-Hindering Biisoquinoline Chelates

Journal article published in 2010 by Fabien Durola ORCID, Jacques Lux, Jean-Pierre Sauvage, Oliver S. Wenger
This paper is available in a repository.
This paper is available in a repository.

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Abstract

In the past, a variety of mechanically interlocked systems such as catenanes and rotaxanes were constructed on the basis of Cu(I) coordination chemistry and endocyclic 1,10-phenanthroline ligands. This review reports on the coordination chemistry of a new family of endocyclic bidentate chelators that are sterically non-hindering, namely 8,8′-diaryl-substituted 3,3′-biisoquinolines. These ligands allow the construction of new multi-component assemblies that are inaccessible with the previously investigated 1,10-phenanthrolines. On the one hand, the sterically non-hindering nature of the new endocyclic chelators makes three-component entanglements around octahedral metal centres such as iron(II), cobalt(II) and ruthenium(II) readily possible. On the other hand, it permits the construction of copper-based molecular shuttles that exhibit shuttling kinetics that excels over those of previously investigated analogous systems with 1,10-phenanthrolines. Thus, within this class of molecular machines, a bigger chelator leads to faster molecular movement, i.e. to a better performance of the molecular machine.