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相关概念视频

Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

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

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

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...
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)01:16

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

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...
Radical Anti-Markovnikov Addition to Alkenes: Overview01:25

Radical Anti-Markovnikov Addition to Alkenes: Overview

The addition of hydrogen bromide to alkenes in the presence of hydroperoxides or peroxides proceeds via an anti-Markovnikov pathway and yields alkyl bromides.
Preparation of Alkynes: Alkylation Reaction02:27

Preparation of Alkynes: Alkylation Reaction

Introduction
Alkylation of terminal alkynes with primary alkyl halides in the presence of a strong base like sodium amide is one of the common methods for the synthesis of longer carbon-chain alkynes. For example, treatment of 1-propyne with sodium amide followed by reaction with ethyl bromide yields 2-pentyne.
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation02:24

Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation

Introduction
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.

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相关实验视频

Updated: May 27, 2026

Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene
09:45

Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene

Published on: March 20, 2017

一个高度选择性的C70形状持久的矩形镜,通过一阶段的基因转化构建.

Chenxi Zhang1, Qi Wang, Hai Long

  • 1Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309, USA.

Journal of the American Chemical Society
|November 17, 2011
PubMed
概括

研究人员开发了一种新的3D分子,COP-5,使用动态共价化学 (DCC) 和基基转化. 这种子有效地结合和分离富勒,对C70比C60具有很高的亲和力和选择性.

科学领域:

  • 超分子化学 超分子化学
  • 有机合成 有机合成
  • 材料科学 材料科学 材料科学

背景情况:

  • 动态共价化学 (DCC) 提供了高效的分子结构,但复杂的3D架构的方法是有限的.
  • 开发强大的方法来创建复杂的分子子对于先进的应用至关重要.

研究的目的:

  • 为了利用基基转化,一种DCC方法,为新型3D分子子的一步合成.
  • 研究合成的富勒结合特性,重点关注亲和力,选择性和可逆性.

主要方法:

  • 使用基甲基合成的3D矩形镜分子COP-5的一步合成.
  • 描述COP-5的结构和形状持久性.
  • 谱分析以确定C60和C70富勒烯的结合常数和选择性.

主要成果:

  • 从基于氨酸的前体中成功合成了新型3D子COP-5的单步合成.
  • COP-5对C60 (1.4 × 10^5 M^-1) 和C70 (1.5 × 10^8 M^-1) 具有很高的结合亲和力.
  • COP-5显示出C70对C60 (K (C70) /K (C60) >1000) 的异常选择性,以及在酸刺激下可逆结合.

结论:

更多相关视频

Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
09:35

Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units

Published on: September 18, 2016

相关实验视频

Last Updated: May 27, 2026

Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene
09:45

Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene

Published on: March 20, 2017

Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units
09:35

Preparation of a Corannulene-functionalized Hexahelicene by Copper(I)-catalyzed Alkyne-azide Cycloaddition of Nonplanar Polyaromatic Units

Published on: September 18, 2016

  • 基基因转化是一种强大的DCC策略,用于构建复杂的3D分子,如COP-5.
  • COP-5是富勒伦的高效纯有机受体,具有前所未有的C70选择性.
  • 可逆结合允许从富勒烯混合物中分离C70,展示了实际应用的潜力.