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相关概念视频

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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Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

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Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
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Polymer Classification: Architecture01:14

Polymer Classification: Architecture

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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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Radical Chain-Growth Polymerization: Chain Branching01:17

Radical Chain-Growth Polymerization: Chain Branching

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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...
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Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

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

Cationic Chain-Growth Polymerization: Mechanism

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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...
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相关实验视频

Updated: Jun 18, 2025

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
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基于分支的寡合体的可逆粘合剂通过可控制的自我聚合来实现.

Chenxi Qin1, Hao Yang1,2, Bin Li1,3

  • 1State Key Laboratory of Solid Lubrication, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou, 730000, China.

Advanced materials (Deerfield Beach, Fla.)
|August 3, 2024
PubMed
概括

研究人员使用分支寡合物开发了一种新的可逆粘合剂. 这种材料实现了超高的粘合强度和广泛的可逆粘合跨度,可通过温度和电压控制.

关键词:
粘附性 粘附性 粘附性 粘附性有分支的寡合体有分支的寡合体动态互动 动态互动电化学 电化学 电化学可逆性的可逆性

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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
  • 粘附科学 粘附科学 粘附科学

背景情况:

  • 超分子粘附材料在平衡强粘附与可逆性方面面临着挑战.
  • 基于小分子的系统在粘附强度,可设计性和相互作用多样性上表现出局限性,这是由于共价键含量低.

研究的目的:

  • 开发一种超高强度和大跨度可逆粘合剂.
  • 通过一种新的策略,克服基于小分子的超分子粘合剂的局限性.

主要方法:

  • 利用一个分支的寡头可控的自我聚合策略.
  • 在寡合体结构中内置密集的共价键.
  • 为了稳定性,采用可逆动态双交叉连接.
  • 研究了温度诱导和电压控制的粘附开关.

主要成果:

  • 实现了大跨度可逆粘附,差异约为140倍.
  • 证明了超强的附着力 (5.58 MPa,5093.92 N m-1) 和超低的附着力 (0.04 MPa,87.656 N m-1).
  • 在100个循环中表现出稳定的可逆粘附过渡.
  • 展示了通过45秒持续时间的8V电压通过粘附的遥控器.

结论:

  • 分支寡合体策略使得超高强度和大跨度可逆粘附成为可能.
  • 密集的共价键增强了强度,而不牺牲可逆性.
  • 开发的粘合剂具有强大的性和特殊的可逆性,适用于先进的应用.