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DOI: 10.1055/s-0036-1588659
Redox Switchable Thianthrene Cavitands
Publication History
Received: 26 October 2016
Accepted: 02 November 2016
Publication Date:
28 November 2016 (online)
Abstract
A redox activated vase-to-kite conformational change is reported for a new resorcinarene-based cavitand appended with four quinoxaline-fused thianthrene units. In its neutral state, the thianthrene-containing cavitand was shown by 1H NMR to adopt a closed vase conformation. Upon oxidation the electrostatic repulsion among the thianthrene radical cations promotes a kite conformation in the thianthrene-containing cavitand. The addition of acid produced a shoulder feature below 300 nm in the cavitand’s UV-Vis spectrum that we have assigned to the vase-to-kite conformation change. UV-Vis spectroelectrochemical studies of the cavitand revealed a development of a similar shoulder peak consistent with the oxidation-induced vase-to-kite conformation change. To support that the shoulder peak is diagnostic for a vase-to-kite conformation change, a model molecule constituting a single quinoxaline wall of the cavitand was synthesized and studied. As expected UV-Vis spectroelectrochemical studies of the cavitand arm did not display a shoulder peak below 300 nm. The oxidation-induced vase-to-kite conformation is further confirmed by the distinctive upfield shift in 1H chemical shift of the methine signal.
Key words
redox active - thianthrene - resorcinarene cavitands - electrochemical switching - conformation changeSupporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0036-1588659.
- Supporting Information
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