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相关概念视频

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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[3,3] Sigmatropic Rearrangement of Allyl Vinyl Ethers: Claisen Rearrangement01:24

[3,3] Sigmatropic Rearrangement of Allyl Vinyl Ethers: Claisen Rearrangement

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The Claisen rearrangement is a [3,3] sigmatropic rearrangement of allyl vinyl ethers to unsaturated carbonyl compounds. The rearrangement is a concerted pericyclic reaction proceeding via a chair-like transition state.
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What is an Electrochemical Gradient?01:26

What is an Electrochemical Gradient?

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Adenosine triphosphate, or ATP, is considered the primary energy source in cells. However, energy can also be stored in the electrochemical gradient of an ion across the plasma membrane, which is determined by two factors: its chemical and electrical gradients.
The chemical gradient relies on differences in the abundance of a substance on the outside versus the inside of a cell and flows from areas of high to low ion concentration. In contrast, the electrical gradient revolves around an...
128.7K
Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis02:29

Ethers from Alcohols: Alcohol Dehydration and Williamson Ether Synthesis

13.0K
Overview
Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.
13.0K
Crown Ethers02:36

Crown Ethers

6.1K
Crown ethers are cyclic polyethers that contain multiple oxygen atoms, usually arranged in a regular pattern. The first crown ether was synthesized by Charles Pederson while working at DuPont in 1967. For this work, Pedersen was co-awarded the 1987 Nobel Prize in Chemistry. Crown ethers are named using the formula x-crown-y, where x is the total number of atoms in the ring and y is the number of ether oxygen atoms. The term 'crown' refers to the crown-like shape that these ether molecules...
6.1K
Structure and Nomenclature of Ethers02:28

Structure and Nomenclature of Ethers

14.9K
Structure and Bonding
Ethers are organic compounds with an ether functional group which is characterized by an oxygen atom connected to two — identical or different — alkyl, aryl, or vinyl groups. The C–O–C linkage in dimethyl ether — the simplest ether — has an approximately tetrahedral bond angle of 110.3 degrees. The oxygen atom is sp3- hybridized, with the C–O distance being about 140 pm.
Classification of Ethers
Based on their attached substituent...
14.9K

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Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
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Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst

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电子化学控制的乙烯基乙烯的阴性聚合

Brian M Peterson1, Song Lin1, Brett P Fors1

  • 1Cornell University , Ithaca, New York 14853, United States.

Journal of the American Chemical Society
|February 1, 2018
PubMed
概括

研究人员使用电化学实现了对阴离子聚合物的时间控制. 这种方法调节了聚合物生长,分子量和分散性,从而实现了块共聚合物合成.

科学领域:

  • 聚合物化学
  • 电化学
  • 材料科学

背景情况:

  • 精确控制聚合物启动,传播和终结对于创建先进材料至关重要.
  • 虽然对激素聚合物建立了电化学控制,但对阴离子聚合物没有实现.
  • 现有的聚合物合成方法通常缺乏对链生长动态的微调控制.

研究的目的:

  • 通过电化学技术来实现对阴离子聚合物的时间控制的方法.
  • 通过电化学手段来调节聚合物分子量和分散性的能力.
  • 通过受控的阴性聚合物合成复杂的聚合物结构,如块共聚物.

主要方法:

  • 使用电化学介质可逆氧化聚合物链末端.
  • 使用稳定的有机基作为中间体和链传递剂.
  • 应用氧化电流来控制聚合过程.

主要成果:

  • 在阴离子聚合过程中对聚合物链生长的时间控制.
  • 控制了聚合物分子重量和分散性.
  • 证实了极好的链末忠实性,促进了块共聚物的合成.

结论:

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  • 现在可以通过介质辅助链末氧化对阴离子聚合物的电化学控制.
  • 这种技术为精确合成具有控制架构的聚合物提供了新的途径.
  • 合成块共聚物的能力为开发新型先进材料开辟了道路.