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相关概念视频

Formation of Halohydrin from Alkenes02:41

Formation of Halohydrin from Alkenes

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An alkene, such as propene, reacts with bromine in the presence of water to yield a halohydrin. Halohydrins contain a halogen and a hydroxyl group attached to adjacent carbons. When the halogen is bromine, it is called a bromohydrin, while a chlorohydrin has chlorine as the halogen.
14.7K
Halogenation of Alkenes02:46

Halogenation of Alkenes

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Halogenation is the addition of chlorine or bromine across the double bond in an alkene to yield a vicinal dihalide. The reaction occurs in the presence of inert and non-nucleophilic solvents, such as methylene chloride, chloroform, or carbon tetrachloride.
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
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Radical Substitution: Allylic Bromination01:27

Radical Substitution: Allylic Bromination

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In organic synthesis, the formation of products can be altered by changing the reaction conditions. For example, a dibromo addition product is formed when propene is treated with bromine at room temperature. In contrast, propene undergoes allylic substitution in non-polar solvents at high temperatures to give 3-bromopropene. In order to avoid the addition reaction, the bromine concentration must be kept as low as possible throughout the reaction. This can be achieved using N-bromosuccinimide...
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Hybridization of Atomic Orbitals I03:24

Hybridization of Atomic Orbitals I

65.8K
The mathematical expression known as the wave function, ψ, contains information about each orbital and the wavelike properties of electrons in an isolated atom. When atoms are bound together in a molecule, the wave functions combine to produce new mathematical descriptions that have different shapes. This process of combining the wave functions for atomic orbitals is called hybridization and is mathematically accomplished by the linear combination of atomic orbitals. The new orbitals that...
65.8K
Hydrogen Bonds01:04

Hydrogen Bonds

13.2K
A hydrogen bond is formed when a weakly positive hydrogen atom already bonded to one electronegative atom (for example, the oxygen in the water molecule) is attracted to another electronegative atom from another polar molecule, such as water (H2O), hydrogen fluoride (HF), or ammonia (NH3). The huge electronegativity difference between the H atom (2.1) and the atom to which it is bonded (4.0 for an F atom, 3.5 for an O atom, or 3.0 for an N atom), combined with the very small size of an H atom...
13.2K
Hydrogen Bonds00:26

Hydrogen Bonds

130.9K
Hydrogen bonds are weak attractions between atoms that have formed other chemical bonds. One of these atoms is electronegative, like oxygen, and has a partial negative charge. The other is a hydrogen atom that has bonded with another electronegative atom and has a partial positive charge.
Hydrogen Bonds Control the World!
Because hydrogen has very weak electronegativity when it binds with a strongly electronegative atom, such as oxygen or nitrogen, electrons in the bond are unequally shared....
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Updated: Jan 18, 2026

From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding
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From Molecules to Materials: Engineering New Ionic Liquid Crystals Through Halogen Bonding

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[NBrN]+类型素结合:从结构到应用

Meimei Zhang1, Xuguan Bai1, Zhennan Tian1

  • 1The Institute for Advanced Studies, Hubei Key Lab on Organic and Polymeric Opto-Electronic Materials, Wuhan University, Wuhan, Hubei, China.

Chemistry (Weinheim an der Bergstrasse, Germany)
|January 16, 2026
PubMed
概括

新兴的[NBrN]+素结合在素结合有机框架 (XOF) 中,在催化和生物医学应用中提供了卓越的性能. 这些Br+桥式XOF显示了未来功能材料设计的巨大潜力.

关键词:
[NBrN]+ 素键的存在素结合有机框架 (XOFs) 是一种有机框架.非对应相互作用的非对应相互作用.这是一个超分子组件.

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Probe Type II Band Alignment in One-Dimensional Van Der Waals Heterostructures Using First-Principles Calculations
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科学领域:

  • 超分子化学 超分子化学
  • 材料科学 材料科学 材料科学
  • 有机化学 有机化学

背景情况:

  • 非共价素结合,特别是[NXN]+动机,在超分子化学中至关重要.
  • 建立了基于I+的系统,但[NBrN]+图案因其独特的特性而受到关注.

研究的目的:

  • 审查素结合有机框架 (XOFs) 中新出现的[NBrN]+动图.
  • 总结一下用于稳定Br+物种的合成策略.
  • 突出 Br+ 桥接 XOF 的优点和应用.

主要方法:

  • 对[NBrN]+图案的合成策略进行了全面的文献综述.
  • 对Br+桥接的XOF进行结构分析.
  • 在催化和生物医学应用中的性能评估.

主要成果:

  • 合成策略包括空间约束,阴离子替代,联结体交换和阳离子调节.
  • [NBrN]+基因表现出较短的NBr键长度和增强的电子缺陷.
  • 在酒精氧化,H2O2生产,抗微生物活性和光热疗法方面,XOFs (Br) 的性能优于I类类似物.

结论:

  • [NBrN]+图案在基于I+的系统上提供了显著的优势.
  • 稳定的Br+桥接XOF在催化和精密医学方面具有巨大的潜力.
  • 这项工作为设计使用Br+桥接XOF的先进功能材料铺平了道路.