Issue 14, 2021

Dual-stimuli pseudorotaxane switches under kinetic control

Abstract

A series of dumbbell-shaped sec-ammonium salts with bulky (pseudo)stoppers (‘speed bumps’) were tested for their ability to form pseudorotaxanes with a redox-switchable, tetrathiafulvalene (TTF)-decorated [24]crown-8 ether. Depending on the size of the pseudostoppers, fast (less than ten minutes), slow (hours to days) and very slow (no pseudorotaxanes observed) threading has been observed. NMR spectroscopy as well as tandem mass spectrometry indicate the formation of non-threaded face-to-face complexes prior to pseudorotaxanes formation. Both isomers can be distinguished by their substantially different stability in collision-induced dissociation (CID) experiments. Two external stimuli affect the stability of the pseudorotaxanes: Deprotonation of the ammonium ion results in fast dethreading, while dethreading is much slower when induced by the charge repulsion upon chemical oxidation of the TTF moiety. Remarkably, the same steric bulk of the pseudostopper thus leads to different dethreading rates depending on the stimulus applied. Based on these findings, two redox-switchable rotaxanes containing a 1-naphthyl and a phenyl moiety as sterically different ‘speed bumps’ in the axle centre were synthesised. Bulk electrolysis of the rotaxanes did not result in the expected macrocycle translocation on the axle independent of the ‘speed bump’ as a remarkable consequence of the mechanical bond.

Graphical abstract: Dual-stimuli pseudorotaxane switches under kinetic control

Supplementary files

Article information

Article type
Research Article
Submitted
31 3月 2021
Accepted
28 4月 2021
First published
29 4月 2021
This article is Open Access
Creative Commons BY license

Org. Chem. Front., 2021,8, 3659-3667

Dual-stimuli pseudorotaxane switches under kinetic control

M. Gaedke, H. Hupatz, H. V. Schröder, S. Suhr, K. F. Hoffmann, A. Valkonen, B. Sarkar, S. Riedel, K. Rissanen and C. A. Schalley, Org. Chem. Front., 2021, 8, 3659 DOI: 10.1039/D1QO00503K

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements