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

Thermal Electrocyclic Reactions: Stereochemistry01:17

Thermal Electrocyclic Reactions: Stereochemistry

2.7K
The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
2.7K
Stability of Conjugated Dienes01:28

Stability of Conjugated Dienes

4.8K
Introduction
A comparison of the enthalpies of hydrogenation of dienes reveals that conjugated dienes release less heat on hydrogenation, rendering them more stable than their nonconjugated analogs.
4.8K
Stability of Substituted Cyclohexanes02:30

Stability of Substituted Cyclohexanes

17.7K
This lesson discusses the stability of substituted cyclohexanes with a focus on energies of various conformers and the effect of 1,3-diaxial interactions.
The two chair conformations of cyclohexanes undergo rapid interconversion at room temperature. Both forms have identical energies and stabilities, each comprising equal amounts of the equilibrium mixture. Replacing a hydrogen atom with a functional group makes the two conformations energetically non-equivalent.
For example, in...
17.7K
Thermal and Photochemical Electrocyclic Reactions: Overview01:26

Thermal and Photochemical Electrocyclic Reactions: Overview

3.3K
Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
3.3K
Woodward–Hoffmann Selection Rules and Microscopic Reversibility01:34

Woodward–Hoffmann Selection Rules and Microscopic Reversibility

4.3K
Electrocyclic reactions, cycloadditions, and sigmatropic rearrangements are concerted pericyclic reactions that proceed via a cyclic transition state. These reactions are stereospecific and regioselective. The stereochemistry of the products depends on the symmetry characteristics of the interacting orbitals and the reaction conditions. Accordingly, pericyclic reactions are classified as either symmetry-allowed or symmetry-forbidden. Woodward and Hoffmann presented the selection criteria for...
4.3K
Cycloaddition Reactions: MO Requirements for Thermal Activation01:16

Cycloaddition Reactions: MO Requirements for Thermal Activation

5.3K
Thermal cycloadditions are reactions where the source of activation energy needed to initiate the reaction is provided in the form of heat. A typical example of a thermally-allowed cycloaddition is the Diels–Alder reaction, which is a [4 + 2] cycloaddition. In contrast, a [2 + 2] cycloaddition is thermally forbidden.
5.3K

You might also read

Related Articles

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

Sort by
Same author

Intra-fractional Voxel-wise Anatomical Motion Tracking Guided by Multimodal Respiratory Surrogates in Radiotherapy: Framework Development and Multi-Center Validation.

International journal of radiation oncology, biology, physics·2026
Same author

Nb-Doped VO<sub>2</sub>-Based Coatings on Glass: Substrate Effects, Thermochromic Performance, and an Effective Transition Temperature for Smart-Glazing Applications.

ACS applied materials & interfaces·2026
Same author

Correction to: The BSSPD 2025 debate: sustainability of dentistry and prosthodontics - is this an emergency?

British dental journal·2026
Same author

Environmental impacts from conventional and digital dental crown fabrication workflows: A comparative life cycle assessment.

Dental materials : official publication of the Academy of Dental Materials·2026
Same author

Hybrid Pickering emulsifiers (HYPIEs) via synergistic water/oil interfacial interactions: enhanced properties and applications.

National science review·2026
Same author

Single-nucleus profiling reveals age-associated remodeling opposed by parity in the postmenopausal human ovary.

bioRxiv : the preprint server for biology·2026

Related Experiment Video

Updated: Apr 20, 2026

Chemical Synthesis of Porous Barium Titanate Thin Film and Thermal Stabilization of Ferroelectric Phase by Porosity-Induced Strain
08:00

Chemical Synthesis of Porous Barium Titanate Thin Film and Thermal Stabilization of Ferroelectric Phase by Porosity-Induced Strain

Published on: March 27, 2018

11.8K

A bistable catanionic system with reinforced thermal stability.

Antoine Simon1, Nicolas Martin2, Jesús Fermín Ontiveros1

  • 1Université De Lille, CNRS, Centrale Lille, Université Artois, UMR 8181 - UCCS - Unité De Catalyse Et Chimie Du Solide, F-59000 Lille, France.

Journal of Colloid and Interface Science
|April 18, 2026
PubMed
Summary
This summary is machine-generated.

We reveal how surfactant ratios control catanionic nanodisc structure and thermal behavior. Adjusting these ratios enables a reversible transition between nanodiscs and vesicles, crucial for material design.

Keywords:
Bilayer interdigitationBistability of self-assemblyCatanionic surfactantNanodisc

More Related Videos

Preparation of Monodomain Liquid Crystal Elastomers and Liquid Crystal Elastomer Nanocomposites
12:21

Preparation of Monodomain Liquid Crystal Elastomers and Liquid Crystal Elastomer Nanocomposites

Published on: February 6, 2016

13.7K
High-Contrast and Fast Photorheological Switching of a Twist-Bend Nematic Liquid Crystal
06:24

High-Contrast and Fast Photorheological Switching of a Twist-Bend Nematic Liquid Crystal

Published on: October 31, 2019

7.0K

Related Experiment Videos

Last Updated: Apr 20, 2026

Chemical Synthesis of Porous Barium Titanate Thin Film and Thermal Stabilization of Ferroelectric Phase by Porosity-Induced Strain
08:00

Chemical Synthesis of Porous Barium Titanate Thin Film and Thermal Stabilization of Ferroelectric Phase by Porosity-Induced Strain

Published on: March 27, 2018

11.8K
Preparation of Monodomain Liquid Crystal Elastomers and Liquid Crystal Elastomer Nanocomposites
12:21

Preparation of Monodomain Liquid Crystal Elastomers and Liquid Crystal Elastomer Nanocomposites

Published on: February 6, 2016

13.7K
High-Contrast and Fast Photorheological Switching of a Twist-Bend Nematic Liquid Crystal
06:24

High-Contrast and Fast Photorheological Switching of a Twist-Bend Nematic Liquid Crystal

Published on: October 31, 2019

7.0K

Area of Science:

  • Colloid and Surface Chemistry
  • Supramolecular Chemistry
  • Materials Science

Background:

  • Catanionic nanodiscs are self-assembled aggregates formed from oppositely charged surfactants.
  • Understanding their formation and behavior is key for developing advanced materials.
  • Previous studies often involved salt, complicating the interpretation of intrinsic behaviors.

Purpose of the Study:

  • To investigate the structural and thermal properties of true catanionic nanodiscs in a salt-free system.
  • To elucidate the role of molar ratio on nanodisc stability and morphology.
  • To establish a link between molecular packing, segregation, and structural transitions.

Main Methods:

  • Small-angle neutron scattering (SANS)
  • Static and dynamic light scattering (SLS/DLS)
  • Differential scanning calorimetry (DSC)
  • Preparation of dispersions at 1 wt% over a molar ratio range (0.25 ≤ r ≤ 0.75)

Main Results:

  • Nanodisc size and stability are governed by molecular edge-face segregation.
  • Compositional asymmetry and chain interdigitation stabilize flat nanodiscs in the crystalline state.
  • Heating induces a reversible transition from discs to vesicles due to suppressed interdigitation and segregation.

Conclusions:

  • Establishes a direct link between interdigitation, compositional segregation, and reversible structural bistability in salt-free catanionic systems.
  • Provides a thermodynamic framework connecting stoichiometry, molecular packing, and aggregate morphology.
  • Enables predictive design of stable catanionic nanodiscs by controlling surfactant ratios.