Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Covalent Bonding and Lewis Structures02:46

Covalent Bonding and Lewis Structures

49.3K
Compared to ionic bonds, which results from the transfer of electrons between metallic and nonmetallic atoms, covalent bonds result from the mutual attraction of atoms for a “shared” pair of electrons.
49.3K
[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction01:16

[4+2] Cycloaddition of Conjugated Dienes: Diels–Alder Reaction

10.2K
The Diels–Alder reaction is an example of a thermal pericyclic reaction between a conjugated diene and an alkene or alkyne, commonly referred to as a dienophile. The reaction involves a concerted movement of six π electrons, four from the diene and two from the dienophile, forming an unsaturated six-membered ring. As a result, these reactions are classified as [4+2] cycloadditions.
10.2K
Dehydration Synthesis01:15

Dehydration Synthesis

133.3K
Overview
Dehydration synthesis (also called a condensation reaction) is the chemical process in which two molecules covalently link together to form a new molecule, along with the release of a water molecule. Many physiologically important compounds form by dehydration synthesis reactions, such as complex carbohydrates, proteins, DNA, and RNA.
Synthesis of carbohydrates
Sugar molecules are covalently linked together by dehydration synthesis. During the reaction, the hydroxyl (-OH) group from...
133.3K
Covalent Bonds01:08

Covalent Bonds

7.4K
Overview
When two atoms share electrons to complete their valence shells, they create a covalent bond. An atom's electronegativity—the force with which shared electrons are pulled towards an atom—determines how the electrons are shared. Molecules formed with covalent bonds can be either polar or nonpolar. Atoms with similar electronegativities form nonpolar covalent bonds; the electrons are shared equally. Atoms with different electronegativities share electrons unequally,...
7.4K
Cycloaddition Reactions: Overview01:16

Cycloaddition Reactions: Overview

2.6K
Cycloadditions are one of the most valuable and effective synthesis routes to form cyclic compounds. These are concerted pericyclic reactions between two unsaturated compounds resulting in a cyclic product with two new σ bonds formed at the expense of π bonds. The [4 + 2] cycloaddition, known as the Diels–Alder reaction, is the most common. The other example is a [2 + 2] cycloaddition.
2.6K
Network Covalent Solids02:18

Network Covalent Solids

13.5K
Network covalent solids contain a three-dimensional network of covalently bonded atoms as found in the crystal structures of nonmetals like diamond, graphite, silicon, and some covalent compounds, such as silicon dioxide (sand) and silicon carbide (carborundum, the abrasive on sandpaper). Many minerals have networks of covalent bonds.
To break or to melt a covalent network solid, covalent bonds must be broken. Because covalent bonds are relatively strong, covalent network solids are typically...
13.5K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Asymmetric Diphosphane Dioxides With A-π-A-π'-D Scaffolds for High-Purity Deep-Blue Luminescence.

Chemistry (Weinheim an der Bergstrasse, Germany)·2026
Same author

Design and application of amino acid-derived aromatic scaffolds in supramolecular covalent and non-covalent systems.

Chemical communications (Cambridge, England)·2026
Same author

Dynamic Control of Nucleic Acids Self-Assembly and Expression Using Photoswitches.

Chemistry (Weinheim an der Bergstrasse, Germany)·2026
Same author

Ligand Side-Chains Control the Formation of an M<sub>8</sub>L<sub>4</sub> Molecular Barrel: Unveiling Selective Encapsulation and Sequential Separation Properties.

Inorganic chemistry·2026
Same author

Programmable Assembly of Multistranded Helices in Water.

Nature communications·2025
Same author

2D Assemblies Based on a Tetraphenylethylene D,L-Cyclic Peptide Scaffold.

Angewandte Chemie (International ed. in English)·2025
Same journal

From cyclic diaryl λ<sup>3</sup>-bromanes/chloranes to polyfuntionalized biarylsilanes <i>via</i> aryne σ-bonds.

Chemical science·2026
Same journal

Non-equilibrium formation of the elusive dibridged diboranyl (B<sub>2</sub>H<sub>5</sub>) radical and boranes in low-temperature diborane ices.

Chemical science·2026
Same journal

Visible-light-driven ruthenium-catalyzed hydrogenation of manganese nitride complexes to ammonia under ambient conditions.

Chemical science·2026
Same journal

Quantification of mesopore infiltration in a polymer-grafted metal-organic framework.

Chemical science·2026
Same journal

Enhanced and selective oxygen reduction by iron porphyrin with a biguanide residue in the second coordination sphere.

Chemical science·2026
Same journal

Excited-state orbital angular momentum enables all-optical molecular spin coherence.

Chemical science·2026
查看所有相关文章

相关实验视频

Updated: Jul 5, 2025

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
09:34

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly

Published on: February 6, 2020

7.3K

动态共价合成 动态共价合成

Fabien B L Cougnon1, Artur R Stefankiewicz2, Sébastien Ulrich3

  • 1Department of Chemistry and Nanoscience Centre, University of Jyväskylä Jyväskylä Finland fabien.b.l.cougnon@jyu.fi.

Chemical science
|January 19, 2024
PubMed
概括
此摘要是机器生成的。

动态共价合成使用可逆键构建复杂分子. 这些适应性结构可以通过刺激来稳定或触发,从而使智能化学系统和分子设备成为可能.

更多相关视频

Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides
07:50

Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides

Published on: May 26, 2019

9.3K
Synthesis of a Water-soluble Metal&#8211;Organic Complex Array
06:40

Synthesis of a Water-soluble Metal–Organic Complex Array

Published on: October 8, 2016

9.9K

相关实验视频

Last Updated: Jul 5, 2025

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
09:34

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly

Published on: February 6, 2020

7.3K
Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides
07:50

Efficient Synthesis of All-Carbon Quaternary Centers via the Conjugate Addition of Functionalized Monoorganozinc Bromides

Published on: May 26, 2019

9.3K
Synthesis of a Water-soluble Metal&#8211;Organic Complex Array
06:40

Synthesis of a Water-soluble Metal–Organic Complex Array

Published on: October 8, 2016

9.9K

科学领域:

  • 化学合成 化学合成
  • 材料科学 材料科学 材料科学
  • 超分子化学 超分子化学

背景情况:

  • 动态共价化学 (DCC) 允许使用可逆共价键进行受控的分子组合.
  • 最近的进步已经扩大了DCC,以创建各种复杂的结构,如宏循环,子和机械互锁的分子.
  • 这些键的可逆性允许刺激反应行为和适应性材料的形成.

研究的目的:

  • 突出动态共价系统的可编程性和多功能性.
  • 展示动态共价组合在创造复杂物质和功能分子装置方面的潜力.
  • 为了强调这些组件的刺激响应性,用于适应性应用.

主要方法:

  • 利用可逆共价键形成用于分子组装.
  • 为特定的结构结果编程动态共价系统.
  • 通过外部刺激 (例如化学,热) 控制债券可逆性.

主要成果:

  • 成功合成了各种复杂的组件,包括宏观循环,子和机械互锁结构.
  • 展示刺激反应行为,使组件能够适应环境变化.
  • 通过关闭债券可逆性来实现稳定,可分离的产品.

结论:

  • 动态共价合成为分子组装提供了精确的控制.
  • 动态共价组件的刺激响应性是设计智能材料和分子设备的关键.
  • 这一领域对创建先进的化学系统和失衡物质具有重大前景.