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Related Concept Videos

Characteristics and Nomenclature of Copolymers01:24

Characteristics and Nomenclature of Copolymers

Copolymers are the products obtained from the polymerization of multiple monomer species. So, in a polymer chain itself, there can be multiple repeating units that come from different monomers. The process of synthesizing a polymer from different monomer species is called copolymerization. When two monomers are involved, the polymer is known as a bipolymer. Polymers with three and four monomers are termed terpolymers and quaterpolymers, respectively. Figure 1 depicts the copolymerization of...
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

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

Cationic Chain-Growth Polymerization: Mechanism

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 generated carbocation,...
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

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,...
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

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 acceptor.
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

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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Amino-acid-based block copolymers by RAFT polymerization.

Hideharu Mori1, Takeshi Endo

  • 1Department of Polymer Science and Engineering, Graduate School of Science and Engineering, Yamagata University, 4-3-16, Jonan, Yonezawa 992-8510, Japan. h.mori@yz.yamagata-u.ac.jp

Macromolecular Rapid Communications
|April 18, 2012
PubMed
Summary
This summary is machine-generated.

Recent advances in amino-acid-based block copolymers synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization are reviewed. This includes stimuli-responsive and self-assembled copolymers with tunable properties and applications.

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Area of Science:

  • Polymer Chemistry
  • Materials Science

Background:

  • Amino-acid-based block copolymers offer unique properties for advanced applications.
  • Reversible Addition-Fragmentation chain transfer (RAFT) polymerization is a versatile technique for synthesizing complex polymer architectures.

Purpose of the Study:

  • To review recent progress in the design and synthesis of amino-acid-based block copolymers using RAFT polymerization.
  • To highlight the development of stimuli-responsive and self-assembled block copolymers with tailored functionalities.

Main Methods:

  • Focus on RAFT polymerization of amino-acid-bearing monomers.
  • Discussion of synthesis strategies for various block copolymer architectures.
  • Exploration of methods for achieving tunable properties.

Main Results:

  • Successful synthesis of pH-, thermo-, and dual-stimuli-responsive block copolymers.
  • Development of amphiphilic and double-hydrophilic block copolymers with tunable chiroptical properties.
  • Creation of copolymers with catalytic, optoelectronic properties, cross-linked micelles, unimolecular micelles, and organic-inorganic hybrids.

Conclusions:

  • RAFT polymerization enables precise control over amino-acid-based block copolymer synthesis.
  • These advanced materials exhibit diverse stimuli-responsive and self-assembly behaviors.
  • The reviewed copolymers hold promise for applications in catalysis, electronics, and nanomedicine.