一种极其稳定的19π形体
Takuya Yoshida1, Wen Zhou2, Taniyuki Furuyama1
1†Department of Chemistry, Graduate School of Science, Tohoku University, Sendai 980-8578, Japan.
Journal of the American Chemical Society
|July 10, 2015
概括
一个稳定的,一个电子减少 ((V) tetraazaporphyrin复合物被分离出来. 这种中性π根表现出19π电子结合系统,通过多种分析技术得到证实.
科学领域:
- 无机化学 无机化学 有机化学
- 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:
- (V) 复合物在各种化学应用中至关重要.
- 二氨酸宏循环具有独特的电子和光物理特性.
- 了解激进物种是开发新型功能材料的关键.
研究的目的:
- 合成和表征一个化的一个电子减少物种 ((V) 酸复合体.
- 为了研究这种新型激进物种的电子结构和特性.
- 为了确认 π 根的性质和联电子电路.
主要方法:
- 空气稳定的减少复合体的隔离和特征.
- 循环电压测量和磁感应度测量.
- 单晶X射线衍射分析.
- 磁圆二极化谱学和理论计算.
主要成果:
- 成功分离一个稳定在空气中的,一个电子减少的复合体.
- 通过电化学和磁性数据确认该物种是中性π基.
- 通过X射线衍射对固态结构的解.
- 光谱和计算证据支持19π电子结合系统.
结论:
- 这项研究成功地合成和表征了一种 ((V) 四二氨酸复合物的新型中性π基.
- 这些发现提供了有关减少类系统的电子结构和稳定性的见解.
- 这项工作有助于理解宏循环化学中的基质物种.
更多相关视频
相关概念视频
Five-Membered Heterocyclic Aromatic Compounds: Overview
6.1K
Heterocyclic aromatic compounds are cyclic compounds that are aromatic and have one or more heteroatoms—atoms other than carbon, in the ring. Depending upon the number of atoms present in the ring, they can be either five or six-membered. Examples of five-membered heterocyclic aromatic compounds include pyrrole, furan, thiophene, and imidazole. Pyrrole consists of one nitrogen atom having one lone pair of electrons. Furan and thiophene have one oxygen and one sulfur heteroatom,...
6.1K
Aromatic Hydrocarbon Anions: Structural Overview
4.4K
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...
Due to the absence of continuous...
4.4K
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
4.1K
The reaction of weakly electrophilic aryldiazonium (also called arenediazonium) salts with highly activated aromatic compounds leads to the formation of products with an —N=N— link, called an azo linkage. This reaction, presented in Figure 1, is known as diazo coupling and occurs without the loss of the nitrogen atoms of the aryldiazonium salt. Highly activated aromatic compounds such as phenols or arylamines favor the diazo coupling reaction. The coupling generally occurs at the para...
4.1K
Aromatic Hydrocarbon Cations: Structural Overview
4.4K
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...
Removing one hydrogen from the intervening CH2 group...
4.4K
Structure of Porins
4.2K
Mitochondria, chloroplasts, and gram-negative bacteria have transmembrane, beta-barrel proteins called porins to mediate the free diffusion of ions and metabolites across the membrane. Mitochondrial porin precursors contain conserved amino acid sequences called beta signals at their C-terminal. Beta signals have a motif of PoXGXXHyXHy (Po-Polar, X-Any amino acid, G-Glycine, Hy-LargeHydrophobic), which are crucial for precursor recognition to initiate precursor assembly. Beta-barrel...
4.2K
Aromatic Compounds: Overview
15.7K
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 isolated...
In 1825, Faraday isolated...
15.7K

![Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60786.jpg&w=3840&q=50)
