Related Experiment Video
Updated: May 16, 2025

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
Published on: June 9, 2023
Molecular Compasses for Modulating Electronic Communication in Pillar[5]quinone
Tae-Woo Kwon1, Guangcheng Wu1, Sheng-Nan Lei1
1Department of Chemistry, The University of Hong Kong, Kowloon 999077, Hong Kong SAR, China.
Abstract:
Just as a pointer, which moves freely and points to the magnetic North in a compass, affords us with a device for tracking direction on a global scale, a dipole moment in a molecule is capable of aligning itself in a compass-like manner in response to an electric field at the molecular level. Here, we demonstrate that dipole moment pointers, based on amide and ester groups in the dumbbell components of [2]rotaxanes, are susceptible to changes in pole-dipole and dipole-dipole interactions within a redox-active pillar[5]quinone ring component when subjected to redox control. Distinct from free pillar[5]quinone, these molecular compasses exhibit a 1-1-1-1-1 electron-uptake pattern during the first-electron transfers. Density functional theory (DFT) calculations reveal that, upon the reduction of quinoid units in the amide-based molecular compass, the positive end of the dipole moment pointer in the dumbbell component becomes oriented toward the reduced anionic quinone in the ring component, courtesy of hydrogen bonding. The negative end of the dipole moment pointer in the dumbbell component lowers the reduction potentials of the other four quinoid units as a result of electrostatic repulsions, which explain its 1-1-1-1-1 electron-uptake pattern. Our findings highlight how electronic communication between the dipole moment pointers and the quinoid units in the ring component enables the [2]rotaxane to act as a molecular compass, precisely reorienting its dipole moments in response to redox changes.
Related Concept Videos
π Electron Effects on Chemical Shift: Overview
UV–Vis Spectroscopy: Molecular Electronic Transitions
Oxidation of Phenols to Quinones
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox...
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds
Negative Regulator Molecules
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation

