A Helicate-Based Three-State Molecular Switch.

Angew Chem Int Ed Engl

Institut für Organische Chemie, RWTH Aachen University, Landoltweg 1, 52074, Aachen, Germany.

Published: September 2018

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.

Download full-text PDF

Source
http://dx.doi.org/10.1002/anie.201806607DOI Listing

Publication Analysis

Top Keywords

helicate-based three-state
4
three-state molecular
4
molecular switch
4
switch control
4
control structural
4
structural transformations
4
transformations triggered
4
triggered external
4
external signals
4
signals development
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!