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Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.4K
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...
2.4K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.1K
The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael...
2.1K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

3.6K
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...
3.6K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

2.6K
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...
2.6K
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

3.4K
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...
3.4K
Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

2.9K
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...
2.9K

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Related Experiment Video

Updated: Aug 10, 2025

Using Polystyrene-block-polyacrylic acid-coated Metal Nanoparticles as Monomers for Their Homo- and Co-polymerization
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Using Polystyrene-block-polyacrylic acid-coated Metal Nanoparticles as Monomers for Their Homo- and Co-polymerization

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Processive Pathways to Metastability in Block Copolymer Thin Films.

Nayanathara Hendeniya1, Kaitlyn Hillery1, Boyce S Chang1

  • 1Department of Materials Science and Engineering, Iowa State University, Ames, IA 50011, USA.

Polymers
|February 11, 2023
PubMed
Summary
This summary is machine-generated.

Block copolymers (BCPs) self-assemble into nanostructures for advanced applications. This review explores solvent and thermal processing pathways to control non-equilibrium BCP phases, expanding structural diversity beyond synthesis.

Keywords:
block copolymermetastablenonequilibriumpost-processingself-assemblysolvent annealingthermal annealing

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Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions

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Area of Science:

  • Materials Science
  • Polymer Chemistry
  • Nanotechnology

Background:

  • Block copolymers (BCPs) self-assemble into complex nanostructures vital for applications like semiconductor processing and membranes.
  • Controlling BCP nanostructures relies on understanding self-assembly kinetics and thermodynamics.
  • While equilibrium structures are well-studied, non-equilibrium phases offer broader structural diversity but are less explored due to stabilization challenges.

Purpose of the Study:

  • To review solvent-induced and thermally induced processing pathways for controlling non-equilibrium block copolymer phases.
  • To highlight the advantages and limitations of these processing techniques.
  • To identify future research directions for inducing and controlling non-equilibrium BCP structures.

Main Methods:

  • Review of existing literature on block copolymer self-assembly.
  • Analysis of solvent-induced processing techniques.
  • Analysis of thermally induced processing techniques.

Main Results:

  • Solvent and thermal processing pathways can influence BCP phase transformations.
  • These pathways offer potential for achieving a wider range of BCP morphologies.
  • Stabilizing non-equilibrium BCP phases remains a significant challenge.

Conclusions:

  • Processing techniques provide an alternative to synthesis for accessing diverse BCP nanostructures.
  • Further investigation into controlled processing is needed to fully exploit non-equilibrium BCP phases.
  • Understanding these pathways can reduce reliance on complex synthesis and improve material compatibility.