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

2.7K
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,...
2.7K
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

3.0K
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...
3.0K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.6K
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...
2.6K
Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

4.2K
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...
4.2K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

4.6K
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...
4.6K

You might also read

Related Articles

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

Sort by
Same author

Photoresponsive Liquid Grippers for Multi-Dimensional Droplet Manipulation.

Small methods·2026
Same author

Nature-Inspired Liquid Crystal Polymer Actuators: From Alignment Regulation to Nano-composition.

Advanced materials (Deerfield Beach, Fla.)·2025
Same author

Shape-Switchable Liquid-Crystal Polymer Actuators with Light-Induced Shape Memory Effect.

ACS applied materials & interfaces·2025
Same author

Liquid crystal polymer actuators with complex and multiple actuations.

Journal of materials chemistry. B·2024
Same author

Dual-Mode Patterns Enabled by Photofluidization of an Azobenzene-Containing Linear Liquid Crystal Copolymer.

Langmuir : the ACS journal of surfaces and colloids·2024
Same author

Photo- and Humidity-Responsive Liquid Crystal Copolymer Actuators Fabricated via Vapor-Assisted Alignment.

ACS applied materials & interfaces·2024

Related Experiment Video

Updated: Mar 9, 2026

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

Visible Light Responsive Liquid Crystal Polymers Containing Reactive Moieties with Good Processability.

Yuyun Liu1, Wei Wu1, Jia Wei1

  • 1Department of Materials Science & State Key Laboratory of Molecular Engineering of Polymers, Fudan University , Shanghai 200433, China.

ACS Applied Materials & Interfaces
|December 22, 2016
PubMed
Summary
This summary is machine-generated.

Novel liquid crystal polymers (LLCPs) were cross-linked to create responsive materials. These cross-linked liquid crystal polymers (CLCPs) exhibit reversible photoinduced bending and unbending when exposed to specific visible light wavelengths.

Keywords:
azotolenegood processabilitylinear polymerliquid crystalphotoinduced deformation

More Related Videos

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

6.9K
Preparation of Liquid Crystal Networks for Macroscopic Oscillatory Motion Induced by Light
07:56

Preparation of Liquid Crystal Networks for Macroscopic Oscillatory Motion Induced by Light

Published on: September 20, 2017

12.2K

Related Experiment Videos

Last Updated: Mar 9, 2026

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

6.9K
Preparation of Liquid Crystal Networks for Macroscopic Oscillatory Motion Induced by Light
07:56

Preparation of Liquid Crystal Networks for Macroscopic Oscillatory Motion Induced by Light

Published on: September 20, 2017

12.2K

Area of Science:

  • Polymer Science
  • Materials Science
  • Photochemistry

Background:

  • Linear liquid crystal polymers (LLCPs) are advanced materials with unique properties.
  • Controlling the cross-linking of LLCPs is crucial for developing photoresponsive materials.
  • Existing methods for creating cross-linked polymers may lack efficiency or versatility.

Purpose of the Study:

  • To synthesize novel reactive linear liquid crystal polymers (LLCPs) with varying azotolene concentrations.
  • To investigate the cross-linking of these LLCPs using difunctional primary amines.
  • To evaluate the photoinduced bending and unbending behaviors of the resulting cross-linked liquid crystal polymers (CLCPs).

Main Methods:

  • Synthesis of two types of reactive linear liquid crystal polymers (LLCPs).
  • Processing of LLCPs into films and fibers via solution and melting methods.
  • Post-cross-linking of LLCPs with difunctional primary amines.
  • Photoresponse testing using 445 nm and 530 nm visible light.

Main Results:

  • Successfully synthesized LLCPs with different azotolene concentrations.
  • Achieved facile cross-linking of LLCPs into cross-linked liquid crystal polymers (CLCPs) in both film and fiber forms.
  • Demonstrated reversible photoinduced bending and unbending of CLCPs upon exposure to 445 nm and 530 nm light at room temperature.
  • Validated the post-cross-linking method for preparing diverse CLCP shapes.

Conclusions:

  • The post-cross-linking approach offers a straightforward route to producing shape-controllable CLCP films and fibers.
  • The developed CLCPs exhibit promising reversible photoactuation, suitable for light-responsive applications.
  • This method allows for the utilization of traditional polymer processing techniques for advanced CLCP materials.