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Related Concept Videos

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 of a...
2.3K
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

2.0K
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...
2.0K
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

3.6K
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...
3.6K
Base-Catalyzed Ring-Opening of Epoxides02:26

Base-Catalyzed Ring-Opening of Epoxides

9.1K
Due to their highly strained structures, epoxides can readily undergo ring-opening reactions through nucleophilic substitution, either in the presence of an acid or a base. The nucleophilic substitution reactions in the presence of acid are called acid-catalyzed ring-opening reactions, and nucleophilic substitution reactions in the presence of a base are called base-catalyzed ring-opening reactions. Epoxides undergo base-catalyzed ring-opening reactions in the presence of a strong nucleophile...
9.1K
Acid-Catalyzed Ring-Opening of Epoxides02:24

Acid-Catalyzed Ring-Opening of Epoxides

7.9K
Epoxides that are three-membered ring systems are more reactive than other cyclic and acyclic ethers. The high reactivity of epoxides originates from the strain present in the ring. This ring strain acts as a driving force for epoxides to undergo ring-opening reactions either with halogen acids or weak nucleophiles in the presence of mild acid. The acid catalyst converts the epoxide oxygen, a poor leaving group, into an oxonium ion, a better leaving group, making the reaction feasible. The...
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Photogeneration of N-Heterocyclic Carbenes: Application in Photoinduced Ring-Opening Metathesis Polymerization
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Advances in heterometallic ring-opening (co)polymerisation catalysis.

Weronika Gruszka1, Jennifer A Garden2

  • 1EaStCHEM School of Chemistry, University of Edinburgh, Edinburgh, UK.

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|June 1, 2021
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Summary

Heterometallic catalysts enhance sustainable plastic production via ring-opening polymerization. This review explores their design, focusing on structure-activity trends for improved performance in creating degradable polymers.

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Area of Science:

  • Polymer Chemistry
  • Organometallic Catalysis
  • Sustainable Materials Science

Background:

  • Truly sustainable plastics necessitate renewable feedstocks, efficient production, and effective end-of-life management.
  • Aliphatic polyesters, polycarbonates, and polyamides are key degradable polymers often synthesized via ring-opening (co)polymerisation (RO(CO)P).
  • Organometallic catalysts are crucial for RO(CO)P, with ongoing research into ligand development.

Purpose of the Study:

  • To review advances in heterometallic catalyst design for RO(CO)P.
  • To highlight structure-activity trends and reactivity patterns in heterometallic catalysts.
  • To provide insights for future development of high-performance catalysts for sustainable polymer synthesis.

Main Methods:

  • Review of existing literature on heterometallic catalysts for RO(CO)P.
  • Analysis of structure-activity relationships in catalyst performance.
  • Identification of reactivity patterns associated with heterometallic systems.

Main Results:

  • Heterometallic catalysts offer significant potential for enhancing activity and selectivity in RO(CO)P compared to homometallic counterparts.
  • Exploration of heterometallic cooperativity is an underexplored yet promising strategy for catalyst improvement.
  • Overarching structure-activity trends and reactivity patterns have been identified.

Conclusions:

  • Heterometallic catalysts are a key strategy for advancing sustainable polymer production.
  • Further research into heterometallic RO(CO)P catalyst design can lead to more efficient and selective polymerization processes.
  • Understanding structure-activity relationships is vital for designing next-generation catalysts for degradable plastics.