| Literature DB >> 30027682 |
Xiaofei Chen1, Thomas M Gerger1, Christoph Räuber1, Gerhard Raabe1, Christian Göb2, Iris M Oppel2, Markus Albrecht1.
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.Entities:
Keywords: catechol ester; helicates; molecular switch; self-assembly; stereochemistry
Year: 2018 PMID: 30027682 DOI: 10.1002/anie.201806607
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336