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

Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael acceptor.
Surface Active Agents01:27

Surface Active Agents

Surfactants, named for their behavior at interfaces, positively adsorb at the interfaces of two phases, reducing interfacial tension. Their versatility as emulsifiers, detergents, and foaming agents stems from this ability. Surfactants, often termed amphiphiles, share the property of amphipathy, with molecules having both hydrophilic and hydrophobic portions. The hydrophilic part is called the head, and the hydrophobic part, including an elongated alkyl substituent, forms the tail.Surfactants...
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the generated carbocation,...
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
Many natural and synthetic polymers are produced by...
Polymer Classification: Stereospecificity01:26

Polymer Classification: Stereospecificity

Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...

You might also read

Related Articles

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

Sort by
Same author

Editorial Comment to Video-urodynamic effects of vibegron, a new selective β3-adrenoceptor agonist, on antimuscarinic-resistant neurogenic bladder dysfunction in patients with spina bifida.

International journal of urology : official journal of the Japanese Urological Association·2021
Same author

Lubrication by Adsorption Films of Hydrophilic Amine-based Protic Ionic Liquids: Effect of Anion Species.

Journal of oleo science·2021
Same author

Oral administration of E-type prostanoid (EP) 1 receptor antagonist suppresses carcinogenesis and development of prostate cancer via upregulation of apoptosis in an animal model.

Scientific reports·2021
Same author

Correlation between a Bedridden Status and the Long-term Outcome in Hemodialysis Patients after Intracerebral Hemorrhaging.

Internal medicine (Tokyo, Japan)·2021
Same author

Regulation of TRPV1 channel activities by intracellular ATP in the absence of capsaicin.

Biochimica et biophysica acta. Biomembranes·2021
Same author

Pathological significance and prognostic role of LATS2 in prostate cancer.

The Prostate·2021

Related Experiment Video

Updated: Jun 21, 2026

Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions
10:53

Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions

Published on: October 10, 2016

Polymerizable anionic gemini surfactants: physicochemical properties in aqueous solution and polymerization behavior.

Kenichi Sakai1, Miyuki Wada, Wataru Matsuda

  • 1Department of Pure and Applied Chemistry in Faculty of Science and Technology and Research Institute for Science and Technology, Tokyo University of Science. k-sakai@rs.noda.tus.ac.jp

Journal of Oleo Science
|July 9, 2009
PubMed
Summary

A novel polymerizable anionic gemini surfactant effectively adsorbs at interfaces and forms stable spherical micelles. These polymerizable micelles can be used as nano-structural templates or stabilizers in aqueous solutions.

More Related Videos

Synthesis of Terpolymers at Mild Temperatures Using Dynamic Sulfur Bonds in Poly(S-Divinylbenzene)
09:16

Synthesis of Terpolymers at Mild Temperatures Using Dynamic Sulfur Bonds in Poly(S-Divinylbenzene)

Published on: May 20, 2019

Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer
10:22

Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer

Published on: November 30, 2020

Related Experiment Videos

Last Updated: Jun 21, 2026

Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions
10:53

Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions

Published on: October 10, 2016

Synthesis of Terpolymers at Mild Temperatures Using Dynamic Sulfur Bonds in Poly(S-Divinylbenzene)
09:16

Synthesis of Terpolymers at Mild Temperatures Using Dynamic Sulfur Bonds in Poly(S-Divinylbenzene)

Published on: May 20, 2019

Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer
10:22

Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer

Published on: November 30, 2020

Area of Science:

  • Materials Science
  • Surface Chemistry
  • Polymer Chemistry

Background:

  • Gemini surfactants offer unique properties due to their dual hydrophobic tails and hydrophilic heads.
  • Anionic surfactants are crucial in various industrial applications, including stabilization and templating.
  • Polymerizable surfactants allow for the creation of stable, structured materials through in-situ polymerization.

Purpose of the Study:

  • To synthesize and characterize a novel polymerizable anionic gemini surfactant (PA12-2-12).
  • To investigate the interfacial behavior and micelle formation of PA12-2-12 in aqueous solutions.
  • To explore the potential of PA12-2-12 as nano-structural organic templates and interfacial stabilizers.

Main Methods:

  • Synthesis of polymerizable anionic gemini surfactant (PA12-2-12).
  • Surface tension measurements to study interfacial adsorption.
  • Corrin-Harkins analysis and cryogenic transmission electron microscopy (cryo-TEM) for micelle characterization.
  • UV light irradiation for polymerization of micelles.

Main Results:

  • PA12-2-12 exhibits effective interfacial adsorption at low concentrations.
  • The polymerizable groups influence molecular packing at the interface, leading to a less packed monolayer.
  • PA12-2-12 forms spherical micelles in aqueous solutions at low electrolyte concentrations.
  • Polymerization of micelles under UV light preserves their spherical morphology.

Conclusions:

  • The synthesized polymerizable anionic gemini surfactant (PA12-2-12) demonstrates unique interfacial properties and micelle-forming behavior.
  • The ability to polymerize micelles in-situ while maintaining their structure opens possibilities for advanced applications.
  • PA12-2-12 shows promise as a building block for novel nanomaterials, acting as templates or stabilizers in aqueous systems.