Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

π Electron Effects on Chemical Shift: Overview01:27

π Electron Effects on Chemical Shift: Overview

1.0K
An applied magnetic field causes loosely bound π-electrons in organic molecules to circulate, producing a local or induced diamagnetic field over a large spatial volume. As the molecules tumble in solution, the field generated by π-electrons in spherical substituents results in a zero net field. However, the net field generated by π-electrons in non-spherical substituents is not zero. The effect of this induced field depends on the orientation of the molecule with respect to B0,...
1.0K
UV–Vis Spectroscopy: Molecular Electronic Transitions01:16

UV–Vis Spectroscopy: Molecular Electronic Transitions

1.3K
In Ultraviolet–Visible (UV–Vis) spectroscopy, the absorption of electromagnetic radiation is used to probe the electronic structure of molecules. This technique provides insights into molecular electronic transitions, particularly the movement of electrons between different molecular orbitals. Radiation is absorbed if the energy of the electromagnetic radiation passing through the molecule is precisely equal to the energy difference between the excited and ground states. During this...
1.3K
Oxidation of Phenols to Quinones01:17

Oxidation of Phenols to Quinones

2.8K
In the presence of oxidizing agents, phenols are oxidized to quinones. Quinones can be easily reduced back to phenols using mild reducing agents. The electron-donating hydroxyl group enhances the reactivity of the aromatic ring, enabling oxidation of the ring even in the absence of an α hydrogen.
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...
2.8K
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds01:14

π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds

1.2K
In aromatic compounds, such as benzene, the circulation of (4n + 2) π-electrons sets up a diamagnetic or diatropic ring current around the perimeter of the molecule. This current induces a magnetic field that opposes the external field inside the ring and reinforces it on the outside. The protons in benzene are deshielded and exhibit high chemical shifts in the range 6.5–8.5 ppm. The shielding effect at the center of the ring is evident in complex aromatic molecules, such as...
1.2K
Negative Regulator Molecules01:23

Negative Regulator Molecules

35.1K
Positive regulators allow a cell to advance through cell cycle checkpoints. Negative regulators have an equally important role as they terminate a cell’s progression through the cell cycle—or pause it—until the cell meets specific criteria.
35.1K
Photochemical Electrocyclic Reactions: Stereochemistry01:26

Photochemical Electrocyclic Reactions: Stereochemistry

1.8K
The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
Selection Rules: Photochemical Activation
1.8K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

A Deep-Red Emissive Cage-in-Rings Complex for Lysosome Imaging.

Angewandte Chemie (International ed. in English)·2026
Same author

A Self-Assembled Cage Binds Xenon via Xe-F Dispersion Interactions.

Journal of the American Chemical Society·2026
Same author

Pretzelanes with Planar Chirality and Guest Recognition Capabilities.

Journal of the American Chemical Society·2025
Same author

Active Transport of Macrocycles into Micelles Using Molecular Pumps.

Angewandte Chemie (International ed. in English)·2025
Same author

33 Unresolved Questions in Nanoscience and Nanotechnology.

ACS nano·2025
Same author

Photoinduced Charge Transfer at Discrete Molecular Interfaces in Cocrystals.

Journal of the American Chemical Society·2025

Related Experiment Video

Updated: May 16, 2025

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
06:53

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks

Published on: June 9, 2023

1.9K

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.

Journal of the American Chemical Society
|April 5, 2025
PubMed
Summary

Molecular compasses using [2]rotaxanes reorient their dipole moments in response to redox changes. This molecular alignment is driven by specific interactions within the redox-active pillar[5]quinone ring component.

More Related Videos

Generation and Coherent Control of Pulsed Quantum Frequency Combs
06:42

Generation and Coherent Control of Pulsed Quantum Frequency Combs

Published on: June 8, 2018

8.9K
Author Spotlight: Advancing Antimicrobial Resistance Research with Innovative Approaches and Synthetic Compounds
05:59

Author Spotlight: Advancing Antimicrobial Resistance Research with Innovative Approaches and Synthetic Compounds

Published on: September 27, 2024

1.8K

Related Experiment Videos

Last Updated: May 16, 2025

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
06:53

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks

Published on: June 9, 2023

1.9K
Generation and Coherent Control of Pulsed Quantum Frequency Combs
06:42

Generation and Coherent Control of Pulsed Quantum Frequency Combs

Published on: June 8, 2018

8.9K
Author Spotlight: Advancing Antimicrobial Resistance Research with Innovative Approaches and Synthetic Compounds
05:59

Author Spotlight: Advancing Antimicrobial Resistance Research with Innovative Approaches and Synthetic Compounds

Published on: September 27, 2024

1.8K

Area of Science:

  • Supramolecular Chemistry
  • Molecular Machines
  • Electrochemistry

Background:

  • Molecular dipole moments can align in response to electric fields, similar to a macroscopic compass.
  • Rotaxanes are mechanically interlocked molecules with potential applications in molecular devices.

Purpose of the Study:

  • To investigate the behavior of molecular compasses based on [2]rotaxanes with dipole moment pointers.
  • To understand how redox control affects dipole-dipole and pole-dipole interactions in these systems.

Main Methods:

  • Synthesis and characterization of [2]rotaxane-based molecular compasses.
  • Electrochemical studies to observe electron-uptake patterns.
  • Density Functional Theory (DFT) calculations to elucidate interaction mechanisms.

Main Results:

  • The molecular compasses exhibit a unique 1-1-1-1-1 electron-uptake pattern during initial electron transfers.
  • DFT calculations show hydrogen bonding directing dipole orientation upon reduction.
  • Electrostatic repulsions from the dipole pointer influence the reduction potentials of the quinoid units.

Conclusions:

  • Electronic communication between dipole moment pointers and quinoid units enables [2]rotaxanes to function as molecular compasses.
  • Redox changes precisely reorient molecular dipole moments, demonstrating controllable molecular alignment.