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Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

2.1K
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...
2.1K
Radical Chain-Growth Polymerization: Chain Branching01:17

Radical Chain-Growth Polymerization: Chain Branching

1.9K
The skeletal structure of polymers synthesized via radical polymerization is always branched. For example, the polymerization of ethylene by radical polymerization results in a low-density grade of polyethylene with a heavily branched skeletal structure. Here, the radical site abstracts hydrogen from the growing chain, and the radical site shifts from the end (a primary carbon center) to anywhere within the growing chain (a secondary carbon center). Consequently, the part of the chain from the...
1.9K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

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

Anionic Chain-Growth Polymerization: Mechanism

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

Ziegler–Natta Chain-Growth Polymerization: Overview

3.2K
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...
3.2K
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

2.3K
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...
2.3K

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Updated: May 20, 2025

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
09:22

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

Published on: February 7, 2017

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通过宏观循环聚类进行分子硬化.

Hang Yin1, Qian Cheng1, Roselyne Rosas2

  • 1State Key Laboratory of Quality Research in Chinese Medicine, Institute of Chinese Medical Sciences, University of Macau Taipa, Macau, China.

Angewandte Chemie (International ed. in English)
|March 25, 2025
PubMed
概括

黄瓜[n]uril宏循环通过控制它们的动力学来选择性地使客分子变硬. 这种宿主与客人的互动为生物灵感系统,室温光和有机催化剂提供了新的策略.

关键词:
黄瓜比图里尔是一种.宏观循环是一种宏观循环.有价值的标准化这是一个超分子的超分子.这是一种四级土壤 (tetratopic).

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Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
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Studying DNA Looping by Single-Molecule FRET
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相关实验视频

Last Updated: May 20, 2025

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
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Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
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科学领域:

  • 超分子化学 超分子化学
  • 化学生物学 化学生物学
  • 材料科学 材料科学 材料科学

背景情况:

  • 体硬化通过控制寡合化来调节蛋白质功能.
  • 在合成化合物中对分子动态的选择性控制具有挑战性.
  • 大自然利用全osteric 机制进行细胞调节.

研究的目的:

  • 为了研究库库比特[n]uril (CB[n]) 宏循环来选择性控制客分子动态.
  • 探索宿主-客人相互作用在硬化分子部分的潜力.
  • 在合成系统中展示一种全控制的新策略.

主要方法:

  • 在H-NMR (1D,2D),DOSY和VT-NMR光谱学中.
  • 异热定位热度计 (ITC) 和质谱仪.
  • 分子建模和计算分析.

主要成果:

  • 库库尔比特[n]乌里尔 (CB[n]) 宏循环广泛地与四重型客分子结合.
  • 主机-客人相互作用选择性地使客分子的不同部分变硬.
  • 黄瓜比特[8]uril (CB[8]) 结合对于客分子部分的选择性硬化至关重要.

结论:

  • 黄瓜[n]urils可以全质地控制分子动力学,模仿自然系统.
  • 这种方法在增强室温光度方面具有潜在的应用.
  • 该策略可能使在水性介质中对有机催化物的全控制成为可能.