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A Helicate‐Based Three‐State Molecular Switch
Authors:Xiaofei Chen  Thomas M. Gerger  Dr. Christoph Räuber  Prof. Dr. Gerhard Raabe  Christian Göb  Prof. Dr. Iris M. Oppel  Prof. Dr. Markus Albrecht
Affiliation:1. Institut für Organische Chemie, RWTH Aachen University, Aachen, Germany;2. Institut für Anorganische Chemie, RWTH Aachen University, Aachen, Germany
Abstract:The control of structural transformations triggered by external signals is important for the development of novel functional devices. In the present study, it is demonstrated that helicates can be designed to structurally respond to the presence of different counterions and to adopt either a compressed or an expanded structure. Reversible switching is not only possible between those two states, furthermore, the twist of the aggregate also can be controlled. Thus, three out of four possible states of a helicate (expanded/left‐handed, expanded/right‐handed, compressed/left‐handed) based on an enantiomerically pure ester bridged dicatecholate ligand are specifically addressed by introduction, exchange, or removal of countercations. This approach is used to reversibly switch between the different states or to successively address them.
Keywords:catechol ester  helicates  molecular switch  self-assembly  stereochemistry
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