循环 π 结合分子及其二离子和单离子二离子的合成和特性
Runjie Xu1, Yoichiro Kuninobu2,1
1Department of Interdisciplinary Engineering Sciences, Interdisciplinary Graduate School of Engineering Sciences, Kyushu University, 6-1 Kasugakoen, Kasuga-shi, Fukuoka 816-8580, Japan.
Organic letters
|June 20, 2024
概括
研究人员使用双Friedel-Crafts反应创造了新的循环 π 结合分子. 这些分子表现出了显著的热稳定性和独特的电子性质,包括近红外吸收在它们的基离子状态.
科学领域:
- 有机化学 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:
- π-结合分子对于有机电子学至关重要.
- 开发稳定,功能性的π-结合系统仍然是一个关键的挑战.
- 弗里德尔-克拉夫茨反应为复杂的有机结构提供了多功能途径.
研究的目的:
- 为了合成新的循环 π 结合分子.
- 研究这些新化合物的结构和电子特性.
- 探索它们在材料科学中的潜在应用.
主要方法:
- 氨基组替代的1,2-bis(2-phenylethynyl) 与一种梅尔德鲁姆酸衍生物的双Friedel-Crafts反应.
- 单晶X射线结构分析用于结构阐明.
- 使用NOBF4进行电化学氧化,以产生基离子和二离子.
主要成果:
- 成功合成和表征了新的循环 π 结合分子.
- 通过单晶X射线衍射来确定分子结构.
- 观察到高热稳定性 (>210°C) 对于一个封闭的外.
- 证明了一个单基离子在溶液中的稳定性,近红外吸收.
结论:
- 合成的循环 π 结合分子具有独特的结构和电子特性.
- 这些化合物具有显著的热稳定性和有趣的氧化还原行为.
- 观察到的近红外吸收表明了光电子应用的潜力.
相关概念视频
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...
Removing one hydrogen from the intervening CH2 group...
2.8K
Pericyclic Reactions: Introduction
8.3K
Pericyclic reactions are organic reactions that occur via a concerted mechanism without generating any intermediates. The reactions proceed through the movement of electrons in a closed loop to form a cyclic transition state, where rearrangement of the σ and π bonds yields specific products.
Pericyclic reactions can be classified into three categories: electrocyclic reactions, cycloaddition reactions, and sigmatropic rearrangements. Electrocyclic reactions and sigmatropic...
Pericyclic reactions can be classified into three categories: electrocyclic reactions, cycloaddition reactions, and sigmatropic rearrangements. Electrocyclic reactions and sigmatropic...
8.3K
Aromatic Hydrocarbon Anions: Structural Overview
2.8K
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...
2.8K
π Molecular Orbitals of the Allyl Cation and Anion
4.2K
An allyl group is a three-carbon conjugated system where the sp³-hybridized allylic carbon is bonded to a CH=CH2 group via a single bond. Allyl anions can be obtained by treating propene with a strong base that can deprotonate methyl groups. Allyl cations are formed as intermediates during substitution reactions involving allylic halides. In both cases, the hybridization of the allylic carbon changes from sp3 to sp2, giving rise to a carbon chain with three sp2-hybridized carbons, each with...
4.2K
Photochemical Electrocyclic Reactions: Stereochemistry
1.8K
The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
Selection Rules: Photochemical Activation
Selection Rules: Photochemical Activation
1.8K
Thermal Electrocyclic Reactions: Stereochemistry
2.0K
The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
2.0K


