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Aromatic Hydrocarbon Anions: Structural Overview01:18

Aromatic Hydrocarbon Anions: Structural Overview

2.7K
Neutral hydrocarbons like cyclopentadiene with an odd number of carbon atoms and one intervening CH2 group in the ring are not aromatic. Cyclopentadiene with 4 π electrons does not satisfy the 4n + 2 π electron rule. Additionally, the intervening CH2 group is sp3 hybridized and lacks a vacant p orbital, thereby interrupting the overlap of p orbitals in a continuous manner and preventing the delocalization of π electrons throughout the ring.
Due to the absence of continuous...
2.7K
Aromatic Hydrocarbon Cations: Structural Overview01:18

Aromatic Hydrocarbon Cations: Structural Overview

2.8K
Cycloheptatriene is a neutral monocyclic unsaturated hydrocarbon that consists of an odd number of carbon atoms and an intervening sp3 carbon in the ring. The three double bonds in the ring correspond to 6 π electrons, which is a Huckel number, and therefore satisfies the criteria of 4n + 2 π electrons. However, the intervening sp3 carbon disrupts the continuous overlap of p orbitals. As a result, cycloheptatriene is not aromatic.
Removing one hydrogen from the intervening CH2 group...
2.8K
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds01:14

π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds

1.2K
In aromatic compounds, such as benzene, the circulation of (4n + 2) π-electrons sets up a diamagnetic or diatropic ring current around the perimeter of the molecule. This current induces a magnetic field that opposes the external field inside the ring and reinforces it on the outside. The protons in benzene are deshielded and exhibit high chemical shifts in the range 6.5–8.5 ppm. The shielding effect at the center of the ring is evident in complex aromatic molecules, such as...
1.2K
Thermal Sigmatropic Reactions: Overview01:16

Thermal Sigmatropic Reactions: Overview

2.1K
Sigmatropic rearrangements are a class of pericyclic reactions in which a σ bond migrates from one part of a π system to another. These are intramolecular rearrangements where the total number of σ and π bonds remain unchanged.
Sigmatropic shifts are classified based on an order term [i, j ], where i and j indicate the number of atoms across which each end of the σ bond migrates. Below are examples of a [3,3] sigmatropic shift in...
2.1K
Aromatic Compounds: Overview01:25

Aromatic Compounds: Overview

10.4K
In general, the term ‘aromatic’ indicates a pleasant smell or fragrance from fresh flowers, freshly prepared coffee, etc. In the early history of organic chemistry, many benzene derivatives were isolated from the pleasant odor oils of the plants. For example, vanillin was isolated from the oil of vanilla, methyl salicylate from the oil of wintergreen, and cinnamaldehyde from the oil of cinnamon. They all had a pleasant odor; hence the name aromatic was given.
In 1825, Faraday...
10.4K
Molecular Models02:00

Molecular Models

37.9K
Physical models representing molecular architectures of chemical compounds play essential roles in understanding chemistry. The use of molecular models makes it easier to visualize the structures and shapes of atoms and molecules.
37.9K

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Updated: Jun 8, 2025

Formation of Ordered Biomolecular Structures by the Self-assembly of Short Peptides
07:26

Formation of Ordered Biomolecular Structures by the Self-assembly of Short Peptides

Published on: November 21, 2013

12.9K

在分子组件和材料中的反芳香性.

Roy Lavendomme1,2, Masahiro Yamashina3

  • 1Laboratoire de Chimie Organique, Université libre de Bruxelles (ULB) Avenue F. D. Roosevelt 50, CP160/06 B-1050 Brussels Belgium roy.lavendomme@ulb.be.

Chemical science
|November 8, 2024
PubMed
概括

反芳香环虽然不稳定,但具有独特的电子特性. 本综述探讨了它们在离散和聚合物组件中的使用,突出了有机电子产品的潜力,并指导了未来的应用.

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Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
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Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates

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Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
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Controlling the Size, Shape and Stability of Supramolecular Polymers in Water

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Last Updated: Jun 8, 2025

Formation of Ordered Biomolecular Structures by the Self-assembly of Short Peptides
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Formation of Ordered Biomolecular Structures by the Self-assembly of Short Peptides

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Construction and Systematical Symmetric Studies of a Series of Supramolecular Clusters with Binary or Ternary Ammonium Triphenylacetates
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Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
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Controlling the Size, Shape and Stability of Supramolecular Polymers in Water

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科学领域:

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

背景情况:

  • 反芳香环以其不稳定性和独特的电子特性而闻名.
  • 这些特性使得它们对基础研究和潜在应用都很有吸引力.
  • 然而,它们固有的不稳定性在合成和处理方面带来了挑战.

研究的目的:

  • 审查使用抗芳香构件的离散和聚合组件.
  • 评估各种抗芳香化合物的适合性,以构建更大的组件.
  • 确定有前途的应用领域,特别是在有机电子领域.

主要方法:

  • 对抗芳香组件现有研究的文献综述.
  • 对组装抗芳香单元的共价和超分子策略的分析.
  • 报告的基本特性和建议应用的评估.

主要成果:

  • 离散的抗芳香组件比聚合物组件更频繁地被研究.
  • 大多数研究都集中在制备和基本性质上,应用开发有限.
  • 现有的抗芳香材料显示出有机电子应用的前景.

结论:

  • 未来的研究应该优先考虑开发利用抗芳香系统独特特性的应用程序.
  • 基于抗芳香材料的材料代表了未来有机电子技术进步的一个有希望的类别.
  • 为非专家提供了关于选择安装抗芳香构建块的指导.