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相关概念视频

Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

3.9K
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...
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Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

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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,...
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Polymer Classification: Stereospecificity01:26

Polymer Classification: Stereospecificity

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Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...
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Characteristics and Nomenclature of Homopolymers01:00

Characteristics and Nomenclature of Homopolymers

3.8K
Polymers that are made up of identical monomer units are called homopolymers. Only one repeating unit is involved in the construction of the homopolymer structure. For example, as depicted in Figure 1, polypropylene is a homopolymer constituted of propylene monomers. Here, the only repeating unit in the polymer chain is propylene.
3.8K
Polymer Classification: Architecture01:14

Polymer Classification: Architecture

3.7K
Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...
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相关实验视频

Updated: Jan 15, 2026

Synthesis of Soft Polysiloxane-urea Elastomers for Intraocular Lens Application
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对于弹性体网络,具有受控终端组的烯功能化聚烯.

Jana Wolf1,2, Patrick M Danner1,2, Dorina M Opris1,2

  • 1Laboratory for Functional Polymers, Swiss Federal Laboratories for Materials Science and Technology (Empa), Ueberlandstrasse 129, 8600 Dübendorf, Switzerland.

ACS polymers Au
|October 13, 2025
PubMed
概括

我们开发了一种新方法来合成具有受控分子量和末端组的高允许性聚氧. 这种方法最大限度地减少循环副产品,提高它们对先进材料应用的适用性.

关键词:
控制的终端组控制的终端组弹性弹性体弹性体是什么化聚氧的化聚氧.极极的多氧化.电性聚合物 电性聚合物

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科学领域:

  • 材料科学 材料科学 材料科学
  • 聚合物化学 聚合物化学

背景情况:

  • 高允许性聚氧对于介电驱动器,传感器,能源设备和电解质至关重要.
  • 一个关键的挑战是合成这些聚合物,以精确的终端组控制和最小的循环含量.

研究的目的:

  • 开发一种可控制分子量和末端组的极性多氧化物合成方法.
  • 为了最大限度地减少在聚氧合成过程中循环副产品的形成.

主要方法:

  • 在无溶剂条件下的 (3-烯) - 甲基二西兰的水解-凝结.
  • 阳离子环开放聚合的孤立的循环多.
  • 量化转化西拉诺尔末端组到阿米诺或维尼尔组.

主要成果:

  • 获得高分子量聚氨酸 (高达25公斤mol-1) 与降低循环含量 (11%的烯提取后).
  • 证明了西兰醇末端组的定量转化为阿米诺 (100%) 和乙烯基 (92%) 组.
  • 成功合成了具有3 - 烯酸侧组的聚氧,并控制了终端组的功能.

结论:

  • 无溶剂合成提供了对聚氧中分子量和循环含量的优越控制.
  • 开发的方法可以生产功能化的聚氧,用于控制的交叉链接到弹性网络中.
  • 这些量身定制的聚氧化对先进的介电和能源应用有前途.