Jove
Visualize
Contact Us

Related Concept Videos

Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
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,...
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...
Classification and Mechanical Properties of Synthetic Polymers01:28

Classification and Mechanical Properties of Synthetic Polymers

Synthetic polymers are classified as elastomers, fibers, or plastics based on their crystallinity. Crystallinity, the degree of long-range order in the solid state, influences the mechanical properties (stretching or contracting) of elastomers. Elastomers are flexible polymers that can expand or contract easily upon the application of an external force. They have numerous crosslinks that pull them back into their original shape when stress is removed. Silicones, for instance, are highly elastic...
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,...
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.

You might also read

Related Articles

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

Sort by
Same author

Spatial effects in polymer chemistry.

Beilstein journal of organic chemistry·2017
Same author

Methylenelactide: vinyl polymerization and spatial reactivity effects.

Beilstein journal of organic chemistry·2017
Same author

From N-vinylpyrrolidone anions to modified paraffin-like oligomers via double alkylation with 1,8-dibromooctane: access to covalent networks and oligomeric amines for dye attachment.

Beilstein journal of organic chemistry·2016
Same author

Amino-functionalized (meth)acryl polymers by use of a solvent-polarity sensitive protecting group (Br-t-BOC).

Beilstein journal of organic chemistry·2016
Same author

A robust platform for functional microgels via thiol-ene achemistry with reactive polyether-based nanoparticles.

Polymer chemistry·2015
Same author

Glucose oxidase and glucose for redox-initiating the free radical copolymerization of N-(ferrocenoylmethyl)acrylamide in aqueous cyclodextrin solution.

Macromolecular rapid communications·2015
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 Experiment Video

Updated: Jun 1, 2026

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
06:44

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding

Published on: March 24, 2018

Polymerizable ionic liquid crystals.

Olga Jazkewitsch1, Helmut Ritter

  • 1Institute of Organic Chemistry and Macromolecular Chemistry II, Heinrich-Heine-University of Duesseldorf, 40225 Duesseldorf, Germany.

Macromolecular Rapid Communications
|June 4, 2011
PubMed
Summary
This summary is machine-generated.

Novel polymerizable vinylimidazolium ionic liquids (ILs) with mesogenic units were synthesized. These ionic liquid crystals (ILCs) exhibit self-assembly into liquid crystalline phases and can be polymerized via a free-radical mechanism.

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

Microfluidic Preparation of Liquid Crystalline Elastomer Actuators
12:04

Microfluidic Preparation of Liquid Crystalline Elastomer Actuators

Published on: May 20, 2018

Related Experiment Videos

Last Updated: Jun 1, 2026

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
06:44

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding

Published on: March 24, 2018

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

Microfluidic Preparation of Liquid Crystalline Elastomer Actuators
12:04

Microfluidic Preparation of Liquid Crystalline Elastomer Actuators

Published on: May 20, 2018

Area of Science:

  • Materials Science
  • Polymer Chemistry
  • Supramolecular Chemistry

Background:

  • Ionic liquids (ILs) are salts with low melting points, offering unique solvent properties.
  • Incorporating mesogenic units into ILs can lead to liquid crystalline behavior.
  • Vinylimidazolium ILs are promising for polymerization due to their reactive vinyl groups.

Purpose of the Study:

  • To synthesize novel polymerizable vinylimidazolium ionic liquids incorporating coumarin and biphenyl mesogenic units.
  • To investigate the liquid crystalline properties induced by these mesogenic units.
  • To explore the polymerization of these ionic liquid crystals.

Main Methods:

  • Synthesis of N-vinylimidazole derivatives with bromoalkylated coumarin and biphenyl units.
  • Characterization of thermal behavior using differential scanning calorimetry (DSC).
  • Analysis of liquid crystalline phases using polarizing optical microscopy (POM).
  • Free-radical polymerization of the synthesized ionic liquid crystals.

Main Results:

  • Successful synthesis of vinylimidazolium ionic liquids with coumarin and biphenyl moieties.
  • Demonstration of self-assembly and liquid crystalline phase formation in the synthesized ILs.
  • Confirmation of polymerizability of the ionic liquid crystals via a free-radical mechanism.

Conclusions:

  • Mesogenic units effectively induce liquid crystalline behavior in vinylimidazolium ionic liquids.
  • The synthesized ionic liquid crystals are amenable to polymerization, opening avenues for new functional materials.
  • This work contributes to the development of advanced liquid crystalline polymers derived from ionic liquids.