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Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)01:16

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

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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...
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Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

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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...
2.0K
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

1.9K
Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
1.9K
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

3.2K
Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
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Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

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Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
2.4K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

2.5K
The radical chain-growth polymerization mechanism consists of three steps: initiation, propagation, and termination of polymerization. The polymerization initiates when a free radical generated from the radical initiator adds to the unsaturated bond in the monomer. The unpaired electron of the free radical and one π electron in the unsaturated bond creates a σ bond between the free radical and the monomer. As a result, the other π electron in the unsaturated bond converts this...
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Related Experiment Video

Updated: Jun 12, 2025

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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Concentration-Driven Ring Expansion Metathesis Polymerization via Tunable Ring Transfer Processes.

Meredith N Pomfret1, Nicholas P Serck1, Lucy P Miller1

  • 1Department of Chemistry and Molecular Engineering and Science Institute, University of Washington, Seattle, Washington 98115, United States.

Journal of the American Chemical Society
|May 27, 2025
PubMed
Summary
This summary is machine-generated.

Ring expansion metathesis polymerization (REMP) using catalyst CB6 produces high-molar-mass cyclic polymers initially, then decreases. This study reveals CB6 acts as both initiator and ring transfer agent, enabling better control over REMP.

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Area of Science:

  • Polymer Chemistry
  • Catalysis
  • Materials Science

Background:

  • Ring expansion metathesis polymerization (REMP) is vital for creating cyclic polymer architectures.
  • Cyclic Ru-benzylidene catalyst CB6 offers enhanced stability and polymerization rates.
  • CB6 exhibits an unusual molar mass evolution, decreasing over time.

Purpose of the Study:

  • To mechanistically understand the polymerization profiles of CB6 in REMP.
  • To investigate the ring transfer steps responsible for CB6's unique molar mass behavior.
  • To establish control over REMP for novel cyclic material development.

Main Methods:

  • Mechanistic studies of CB6 polymerization.
  • Analysis of molar mass evolution profiles.
  • Investigation of reaction concentration effects.

Main Results:

  • CB6 acts as both an initiator and a catalytic ring transfer agent.
  • An intricate relationship between reaction concentration and molar mass was identified.
  • High molar mass cyclic polymers are formed early, followed by a decrease.

Conclusions:

  • A deeper mechanistic understanding of REMP with CB6 was achieved.
  • Control over REMP is enhanced through understanding catalyst behavior.
  • This work provides a toolkit for optimizing catalyst design and creating new cyclic materials.