Switchable synchronisation of pirouetting motions in a redox-active [3]rotaxane. Issue 45 (14th November 2018)

• Record Type: Journal Article
• Authors: Schröder, Hendrik V.; Mekic, Amel; Hupatz, Henrik; Sobottka, Sebastian; Witte, Felix; Urner, Leonhard H.; Gaedke, Marius; Pagel, Kevin; Sarkar, Biprajit; Paulus, Beate; Schalley, Christoph A.
• Is Part Of: Nanoscale. Volume 10:Issue 45(2018)
• Page Start: 21425
• Page End: 21433
• Publication Date: 2018-11-14
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/c8nr05534c
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : A redox-active [3]rotaxane is reported, in which wheel pirouetting motions can be synchronised by electrochemical switching. Abstract : In this study, the crown/ammonium [3]rotaxaneR2 is reported which allows a switchable synchronisation of wheel pirouetting motions. The rotaxane is composed of a dumbbell-shaped axle molecule with two mechanically interlocked macrocycles which are decorated with a redox-active tetrathiafulvalene (TTF) unit. Electrochemical, spectroscopic, and electron paramagnetic resonance experiments reveal that rotaxaneR2 can be reversibly switched between four stable oxidation states (R2, R2 ˙ +, R2 2( ˙ +), andR2 4+ ). The oxidations enable non-covalent, cofacial interactions between the TTF units in each state—including a stabilised mixed-valence (TTF2 )˙ + and a radical-cation (TTF˙ + )2 dimer interaction—which dictate a syn (R2, R2 ˙ +, andR2 2( ˙ +) ) or anti (R2 4+ ) ground state co-conformation of the wheels in the rotaxane. Furthermore, the strength of these wheel–wheel interactions varies with the oxidation state, and thus electrochemical switching allows a controllable synchronisation of the wheels' pirouetting motions. DFT calculations explore the potential energy surface of the counter-rotation of the two interacting wheels in all oxidation states. The controlled coupling of pirouetting motions in rotaxanes can lead to novel molecular gearing systems which transmit rotational motion by switchable non-covalent interactions.