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Updated: Jul 9, 2025

Direct Imaging of Laser-driven Ultrafast Molecular Rotation
Published on: February 4, 2017
Orthogonal Initiation of Molecular Motion Devices by Two Chemical Fuels
Debabrata Mondal1, Sohom Kundu1, Emad Elramadi1
1Center of Micro- and Nanochemistry and (Bio)Technology (Cμ), Organische Chemie I, School of Science and Engineering, University of Siegen, Adolf-Reichwein-Str. 2, D-57068 Siegen, Germany.
Abstract:
Herein, we demonstrate the selective dissipative and orthogonal actuation of two distinct molecular devices controlled by alternate fuel use. When the multicomponent ensemble of [2]rotaxane 1 and turnstile [Cu(2)(3)]+ was charged with AgBF4 as chemical fuel (Fuel 1) together with NEt3/PhCH2Br (cofuels), the transiently formed [Ag(1)]+ showed a stochastic shuttling of the silver macrocycle between two degenerate triazole stations on the thread (k298 = 1.2 × 105 s-1), whereas [Cu(2)(3)]+ was unperturbed. Instead, treatment of the mixture with PPh3 as an alternative fuel (Fuel 2) in the presence of oxidant 4 (cofuel) generated the complex [Cu(3)(PPh3)2]+ and transient thermal motion in rotor 2 (k298 = 4.9 × 104 s-1), whereas rotaxane 1 stayed dormant. Thus, two distinct chemical fuels selectively and orthogonally activated two distinct transient motion devices from a multicomponent mixture. In total, four interference-free dissipative cycles were demonstrated by using alternating fuel additions.
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