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Polymer Classification: Architecture01:14

Polymer Classification: Architecture

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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...
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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
Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

2.3K
Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...
2.3K
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
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)01:16

Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)

2.8K
Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring...
2.8K
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

8.4K
The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
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Updated: Oct 5, 2025

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

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Highly Impact-Resistant Block Polymer-Based Thermoplastic Elastomers with an Ionically Functionalized Rubber Phase.

Takato Kajita1, Atsushi Noro1,2, Ryoji Oda3

  • 1Department of Molecular & Macromolecular Chemistry, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, Nagoya 464-8603, Japan.

ACS Omega
|January 31, 2022
PubMed
Summary

New ionically functionalized elastomers (i-SIS) demonstrate high tensile toughness and excellent impact resistance. These materials, synthesized at scale, show promise as advanced, durable elastomeric solutions.

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The Preparation and Properties of Thermo-reversibly Cross-linked Rubber Via Diels-Alder Chemistry
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Area of Science:

  • Materials Science
  • Polymer Chemistry

Background:

  • Elastomers with noncovalent bonding groups show high strength but lack impact resistance data.
  • Large-scale synthesis of such advanced elastomers has been a significant challenge.

Purpose of the Study:

  • To develop and evaluate ionically functionalized elastomers with enhanced mechanical properties, including impact resistance.
  • To establish a scalable synthetic route for these novel materials.

Main Methods:

  • Ionization of the rubber phase in polystyrene-block-polyisoprene-block-polystyrene (SIS) to create ionically functionalized elastomers.
  • Preparation of elastomers with sodium (i-SIS(Na)) and barium (i-SIS(Ba)) cations.
  • Evaluation of tensile toughness, compressive resistance, and impact resistance.

Main Results:

  • Synthesized several tens of grams of i-SIS(Na) and i-SIS(Ba) elastomers.
  • Achieved high tensile toughness: 520 MJ m⁻³ for i-SIS(Na) and 280 MJ m⁻³ for i-SIS(Ba).
  • Demonstrated superior impact resistance for i-SIS(Ba) compared to glass fiber-reinforced plastic.

Conclusions:

  • Ionically functionalized elastomers exhibit exceptional tensile toughness and compressive resistance.
  • i-SIS(Ba) offers significant advantages in impact protection, surpassing conventional materials.
  • Scalable production potential positions these elastomers as next-generation materials.