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相关概念视频

Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

4.5K
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...
4.5K
Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

2.9K
Step growth polymerization involves bi or multifunctional monomers. Bifunctional monomers react to form linear step growth polymers, whereas multifunctional monomers react to form non-linear or branched polymers.
As the step-growth polymerization involves step-wise condensation of monomers, the molecular weight also builds up eventually. Consequently, high molecular weight polymers are obtained at the late stages of the polymerization, where 99% of monomers have been consumed.
The extent of the...
2.9K
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)01:16

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

3.2K
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...
3.2K
Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

2.7K
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...
2.7K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

3.7K
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...
3.7K
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

3.0K
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...
3.0K

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相关实验视频

Updated: Mar 3, 2026

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
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Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly

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种子寡合体通过模板效应调节序列发育,在模拟不可逆转的阶段增长共聚化中进行模拟.

Wenxin Xu1, Nhu Q Nguyen1,2, Kateri H DuBay1

  • 1Department of Chemistry, University of Virginia, Charlottesville, Virginia 22904, United States.

Macromolecules
|March 2, 2026
PubMed
概括

将预制种子链添加到阶段生长共聚合物中,会影响最终的聚合物序列. 这种模板效应取决于种子特性,溶剂粘度和反应障碍,为改善序列控制提供了一条途径.

科学领域:

  • 聚合物化学 聚合物化学
  • 材料科学 材料科学 材料科学
  • 计算化学计算化学

背景情况:

  • 共聚合物序列决定了材料特性,需要对合成序列进行控制.
  • 预制种子模板是对测序控制聚合物的有希望的策略.
  • 新兴的自我模板效应源于链条的刚性和链际吸引力.

研究的目的:

  • 直接研究预成形种子链在阶段生长共聚合中的模板效应.
  • 了解种子特征如何影响序列控制.
  • 识别影响反应动力学和微相分离的因素.

主要方法:

  • 模拟不可逆转的阶段增长共聚变.
  • 包括具有不同性质的预制种子链.
  • 分析出现的微相分离和反应动力学.

主要成果:

  • 种子链的添加显著影响最终的共聚合物序列.
  • 新兴的微相分离和反应动力学受到种子添加的影响.
  • 最后的序列对种子序列,长度,刚度,溶剂粘度和反应障碍敏感.

结论:

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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
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Protocol for the Solid-phase Synthesis of Oligomers of RNA Containing a 2'-O-thiophenylmethyl Modification and Characterization via Circular Dichroism
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Protocol for the Solid-phase Synthesis of Oligomers of RNA Containing a 2'-O-thiophenylmethyl Modification and Characterization via Circular Dichroism

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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

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  • 预制的种子链提供了一种可行的方法,以增强阶段生长共聚化中的序列控制.
  • 了解种子特性和反应条件的相互作用对于优化模板设计至关重要.
  • 这种方法提供了一个潜在的简单路线,精确设计的共聚合物序列.