Related Experiment Video
Updated: Nov 11, 2025

Light-driven Molecular Motors on Surfaces for Single Molecular Imaging
Published on: March 13, 2019
Multitasking with Chemical Fuel: Dissipative Formation of a Pseudorotaxane Rotor from Five Distinct Components
Amit Ghosh1, Indrajit Paul1, Michael Schmittel1
1Center of Micro- and Nanochemistry and Engineering, Organische Chemie I, Universität Siegen, Adolf-Reichwein-Strasse 2, D-57068 Siegen, Germany.
Abstract:
A 3-fold completive self-sorted library of dynamic motifs was integrated into the design of the pseudorotaxane-based rotor [Zn(2·H+)(3)(4)]2+ operating at k298 = 15.4 kHz. The rotational motion in the five-component device is based on association/dissociation of the pyridyl head of the pseudorotaxane rotator arm between two zinc(II) porphyrin stations. Addition of TFA or 2-cyano-2-phenylpropanoic acid as a chemical fuel to a zinc release system and the loose rotor components 2-4 enabled the liberated zinc(II) ions and protons to act in unison, setting up the rotor through the formation of a heteroleptic zinc complex and a pseudorotaxane linkage. With chemical fuel, the dissipative system was reproducibly pulsed three times without a problem. Due to the double role of the fuel acid, two kinetically distinct processes played a role in both the out-of-equilibrium assembly and disassembly of the rotor, highlighting the complex issues in multitasking of chemical fuels.
Related Concept Videos
Woodward–Hoffmann Selection Rules and Microscopic Reversibility
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)
Thermal and Photochemical Electrocyclic Reactions: Overview
Radical Chain-Growth Polymerization: Mechanism
Radical Formation: Overview
Radicals from spin-paired molecules:
Radicals can be obtained from spin-paired molecules either by homolysis or electron transfer. While two radicals are formed in the former, an electron is added in the...
Radical Reactivity: Overview

