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Related Concept Videos

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 of a...
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Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

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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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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...
3.1K
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.8K
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...
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Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

3.4K
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 species into...
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Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

3.2K
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...
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Updated: Jan 19, 2026

Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex
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Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex

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Polymerizations Mediated by Well-Defined Rhodium Complexes.

Nicholas Sheng Loong Tan1, Andrew B Lowe1

  • 1Curtin Institute for Functional Molecules and Interfaces (CIFMI) & School of Molecular and Life Sciences (MLS), Curtin University, Bentley, Perth, WA, 6102, Australia.

Angewandte Chemie (International Ed. in English)
|September 26, 2019
PubMed
Summary
This summary is machine-generated.

This review covers Rhodium(I) complexes for polymerization of alkynes, isocyanides, and esters. These catalysts enable controlled synthesis of advanced polymer materials.

Keywords:
arylisocyanidescontrolled polymerizationpolyphenylacetylenesrhodium complexesstereoregularity

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Synthesis of a Water-soluble Metal&#8211;Organic Complex Array
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Area of Science:

  • Polymer Chemistry
  • Organometallic Chemistry

Background:

  • Rhodium(I) complexes are effective catalysts for polymerization reactions.
  • Controlled polymerization of unsaturated monomers is crucial for advanced materials.

Purpose of the Study:

  • To review the state-of-the-art in Rh(I)-mediated (co)polymerizations.
  • To highlight Rh(I) complexes for specific monomer classes.

Main Methods:

  • Review of literature on Rh(I)-catalyzed polymerizations.
  • Focus on ethynyl, vinyl, and aryl Rh(I) complexes.

Main Results:

  • Detailed overview of Rh(I) complexes for phenylacetylene polymerization.
  • Discussion of Rh(I) species for arylisocyanide and propargyl ester/amide polymerization.

Conclusions:

  • Rh(I) complexes offer versatile catalytic pathways for polymer synthesis.
  • Well-defined Rh(I) systems are key to controlling polymer structure and properties.