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Polymer Classification: Architecture01:14

Polymer Classification: Architecture

3.1K
Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...
3.1K
Polymer Classification: Stereospecificity01:26

Polymer Classification: Stereospecificity

2.7K
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...
2.7K
Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

3.2K
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...
3.2K
Characteristics and Nomenclature of Copolymers01:24

Characteristics and Nomenclature of Copolymers

2.7K
Copolymers are the products obtained from the polymerization of multiple monomer species. So, in a polymer chain itself, there can be multiple repeating units that come from different monomers. The process of synthesizing a polymer from different monomer species is called copolymerization. When two monomers are involved, the polymer is known as a bipolymer. Polymers with three and four monomers are termed terpolymers and quaterpolymers, respectively. Figure 1 depicts the copolymerization of...
2.7K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

3.8K
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...
3.8K
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.2K
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,...
2.2K

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Related Experiment Video

Updated: Oct 4, 2025

Synthesis of Programmable Main-chain Liquid-crystalline Elastomers Using a Two-stage Thiol-acrylate Reaction
11:17

Synthesis of Programmable Main-chain Liquid-crystalline Elastomers Using a Two-stage Thiol-acrylate Reaction

Published on: January 19, 2016

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Topological alternation from structurally adaptable to mechanically stable crosslinked polymer.

Wei-Hsun Hu1,2, Ta-Te Chen2,3, Ryo Tamura4

  • 1Research and Services Division of Materials Data and Integrated System (MaDIS), National Institute for Materials Science (NIMS), Ibaraki, Japan.

Science and Technology of Advanced Materials
|February 7, 2022
PubMed
Summary

Researchers developed a dynamic polymer that can change shape and resist creep. By altering its network structure with heat, the material gains dimensional stability, enhancing its use in advanced devices.

Keywords:
20 Organic and soft materials (colloids, liquid crystals, gel, polymers)301 Chemical syntheses / processing < 300 Processing / Synthesis and Recycling501 Chemical analyses < 500 CharacterizationCovalent adaptable network polymercreep deformationshape-morphing polymer materialtopological alternation

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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

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Related Experiment Videos

Last Updated: Oct 4, 2025

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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

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Area of Science:

  • Materials Science
  • Polymer Chemistry
  • Mechanical Engineering

Background:

  • Stimuli-responsive polymers with controllable shape-morphing are crucial for engineering applications.
  • Dynamic cross-linked polymers offer shape-morphing via solid-state plasticity but suffer from creep deformation and dimensional instability.

Purpose of the Study:

  • To develop a dynamic cross-linked polymer with tunable creep behavior and enhanced dimensional stability.
  • To investigate a topological alternation mechanism for reducing creep in shape-morphing polymers.

Main Methods:

  • Utilized a thermally triggered disulfide-ene reaction to alter the polymer's network topology.
  • Evaluated shape-morphing capabilities at 130°C for topological rearrangement (dynamic state).
  • Assessed creep reduction after topological alternation to a static state at 180°C.

Main Results:

  • The polymer exhibited topological rearrangement for plasticity at 130°C.
  • Creep deformation was reduced by over 85% after topological alternation to a static network at 180°C.
  • The material demonstrated shape-morphing ability combined with enhanced creep resistance.

Conclusions:

  • Sequential topological alternation allows for temperature-dependent control over shape-morphing and creep resistance.
  • This design enhances dimensional stability and service longevity of dynamic covalent polymers.
  • The developed polymer expands possibilities for fabricating sophisticated multifunctional devices.