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

Cycloaddition Reactions: MO Requirements for Photochemical Activation01:12

Cycloaddition Reactions: MO Requirements for Photochemical Activation

2.1K
Some cycloaddition reactions are activated by heat, while others are initiated by light. For example, a [2 + 2] cycloaddition between two ethylene molecules occurs only in the presence of light. It is photochemically allowed but thermally forbidden.
2.1K
Molecular Models02:00

Molecular Models

38.7K
Physical models representing molecular architectures of chemical compounds play essential roles in understanding chemistry. The use of molecular models makes it easier to visualize the structures and shapes of atoms and molecules.
38.7K
Thermal and Photochemical Electrocyclic Reactions: Overview01:26

Thermal and Photochemical Electrocyclic Reactions: Overview

2.4K
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.
2.4K
Photochemical Electrocyclic Reactions: Stereochemistry01:26

Photochemical Electrocyclic Reactions: Stereochemistry

1.9K
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
1.9K
SN2 Reaction: Mechanism02:27

SN2 Reaction: Mechanism

14.5K
The kinetic studies of SN2 reactions suggest an essential feature of its mechanism: it is a single-step process without intermediates. Here, both the nucleophile and the substrate participate in the rate-determining step.
The presence of the more electronegative halogen in the substrate creates a polarized carbon-halide bond. The halide pulls the electron cloud generating an electrophilic center at the carbon atom. Thus, the carbon atom carries a partial positive charge while the halide has a...
14.5K
Properties of Organometallic Compounds01:23

Properties of Organometallic Compounds

1.1K
Organometallic compounds are compounds that contain a carbon–metal bond. Carbon belongs to an organyl group like alkyl, aryl, allyl, or benzyl groups. The metal can be from Group I or Group II of the periodic table, a transition metal, or a semimetal.
1.1K

You might also read

Related Articles

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

Sort by
Same author

Reversible Nucleolar Complex Coacervation by Short Cationic Peptides.

Journal of the American Chemical Society·2026
Same author

Enzyme-Free Phosphorylation with Kinetic Gating in a De Novo Coiled-Coil System.

Journal of the American Chemical Society·2026
Same author

Design of Fuel-Dependent, Complex-Coacervate-Based Synthetic Cells.

Chemistry (Weinheim an der Bergstrasse, Germany)·2026
Same author

DNA affects the phenotype of fuel-dependent coacervate droplets.

Nature communications·2026
Same author

Molecular Design in l-Glutamic Acid-Based Peptide Assembly Dynamics Driven by Carbodiimide-Fueled Reaction Cycle.

Biomacromolecules·2026
Same author

Chemically Fueled, Active Droplets Prevent the Aging of Peptides into Amyloid-Like Fibers.

Journal of the American Chemical Society·2025
Same journal

Particle-Nanofiber Superstructures.

Accounts of materials research·2026
Same journal

Aqueous Processing of Stoichiometric and Nonstoichiometric Materials from Complex Coacervates.

Accounts of materials research·2026
Same journal

Mitigating Interfacial Contamination for Scalable Integration of Graphene in Neuroelectronic Devices.

Accounts of materials research·2026
Same journal

Harnessing Metal-Halide Layered Perovskite Structures for Next-Generation Lighting Sources.

Accounts of materials research·2026
Same journal

Innovative Applications Enabled by the Versatile Structural Color of Cholesteric Liquid Crystals.

Accounts of materials research·2026
Same journal

A Transformation-First Roadmap for Safe and Sustainable Emerging Advanced Materials.

Accounts of materials research·2026
See all related articles

Related Experiment Video

Updated: Jul 28, 2025

Synthesis and Characterization of Supramolecular Colloids
09:26

Synthesis and Characterization of Supramolecular Colloids

Published on: April 22, 2016

9.9K

Chemically Fueled Supramolecular Materials.

Xiaoyao Chen1, Michaela A Würbser1, Job Boekhoven1

  • 1Department of Chemistry, School of Natural Sciences, Technical University of Munich, Lichtenbergstrasse 4, 85748 Garching bei München, Germany.

Accounts of Materials Research
|May 31, 2023
PubMed
Summary
This summary is machine-generated.

Chemically fueled assemblies use fuel molecules to drive self-assembly processes, mimicking biological systems. A new carbodiimide-driven cycle offers a simple, versatile method for creating dynamic supramolecular materials with unique properties.

More Related Videos

Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
16:24

Controlling the Size, Shape and Stability of Supramolecular Polymers in Water

Published on: August 2, 2012

18.7K
Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
06:35

Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates

Published on: February 15, 2016

8.2K

Related Experiment Videos

Last Updated: Jul 28, 2025

Synthesis and Characterization of Supramolecular Colloids
09:26

Synthesis and Characterization of Supramolecular Colloids

Published on: April 22, 2016

9.9K
Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
16:24

Controlling the Size, Shape and Stability of Supramolecular Polymers in Water

Published on: August 2, 2012

18.7K
Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
06:35

Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates

Published on: February 15, 2016

8.2K

Area of Science:

  • Supramolecular Chemistry
  • Materials Science
  • Chemical Biology

Background:

  • Biological molecules are regulated by nonequilibrium chemical reaction cycles, such as phosphorylation.
  • These cycles power dynamic self-assembly processes, leading to unique material properties like self-healing.
  • Creating synthetic chemically fueled assemblies is challenging due to the complexity of reaction cycles.

Purpose of the Study:

  • To introduce a versatile and user-friendly carbodiimide-driven reaction cycle for chemically fueled assemblies.
  • To provide design principles for building blocks and strategies for creating diverse supramolecular materials.
  • To explore reciprocal feedback mechanisms between assemblies and their reaction cycles.

Main Methods:

  • Development of a carbodiimide-based reaction cycle involving a carboxylate precursor and a carbodiimide.
  • Design of building blocks to control assembly formation and material morphology.
  • Investigation of self-healing properties and reciprocal coupling in the formed supramolecular structures.

Main Results:

  • A simplified, quantitatively understood carbodiimide-driven reaction cycle that avoids side reactions.
  • Successful creation of various morphologies including fibers, colloids, crystals, and droplets.
  • Demonstration of unique material properties, such as self-healing, in the assembled structures.

Conclusions:

  • The carbodiimide-driven cycle democratizes the field of chemically fueled assemblies.
  • This approach enables the rational design of novel supramolecular materials with tunable properties.
  • The findings facilitate further progress toward conceptually new dynamic and responsive materials.