二 (利) 盐的战略合成和超分子组织
Elizaveta V Knyazeva1, Natalia S Soldatova1, Pavel A Abramov1,2
1Research School of Chemistry and Applied Biomedical Sciences, Tomsk Polytechnic University, Tomsk 634034, Russian Federation.
The Journal of organic chemistry
|October 30, 2025
概括
研究人员使用m-CPBA氧化开发了一种多功能合成工具包,用于arylenebis ((aryliodonium) 盐. 这种方法为各种基质提供了高效的合成途径,为水晶工程应用产生高纯度化合物.
科学领域:
- 有机合成 有机合成
- 超分子化学 超分子化学
- 晶体工程 晶体工程
背景情况:
- 二 (二) 盐是有机合成中的重要前体.
- 开发这些化合物的高效和多功能合成途径仍然是一个挑战.
- 了解它们的固态行为对于晶体工程应用至关重要.
研究的目的:
- 开发一套全面的合成工具包,用于制备基 (aryliodonium) 盐.
- 建立多功能合成路径,适应不同的基质特性.
- 研究这些盐的超分子组织和潜在应用.
主要方法:
- 通过m-CPBA氧化,从二二烯中合成二 (二) 盐.
- 基于中间溶解度的单和两阶段合成途径的开发.
- 使用分析技术和X射线晶体学对合成化合物的表征.
主要成果:
- 为二 (aryliodonium) 盐建立了一个多功能合成工具包.
- 优化了四种不同的合成方法,以适应不同的烯和二烯基底.
- 实现了 bis () 盐的高产量 (高达99%).
- X射线晶体学通过素结合揭示了1D链的形成,这表明了晶体工程的潜力.
结论:
- 开发的方法提供了一个高效和可适应的途径,以arylenebis ((aryliodonium) 盐.
- 合成的盐表现出有趣的超分子结构,由素结合驱动.
- 这些化合物作为先进的晶体工程应用的有价值的构建块.
相关概念视频
Nucleophilic Aromatic Substitution of Aryldiazonium Salts: Aromatic SN1
2.6K
Treating arylamines with nitrous acid gives aryldiazonium salts that are effective substrates in nucleophilic aromatic substitution reactions. The diazonio group in these salts can be easily displaced by different nucleophiles, yielding a wide variety of substituted benzenes. The leaving group departs as nitrogen gas, and this easy elimination is the driving force for the substitution reaction.
In the Sandmeyer reaction, for example, the diazonio group is replaced by a chloro, bromo,...
In the Sandmeyer reaction, for example, the diazonio group is replaced by a chloro, bromo,...
2.6K
Aryldiazonium Salts to Azo Dyes: Diazo Coupling
3.6K
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...
3.6K
Diazonium Group Substitution with Halogens and Cyanide: Sandmeyer and Schiemann Reactions
2.4K
Arenediazonium substitution reactions occur when the diazonium group is substituted by various functional groups such as halides, hydroxyl, nitrile, etc. For instance, arenediazonium salts react with copper(I) salts of chloride, bromide, or cyanide to form corresponding aryl chlorides, bromides, and nitriles. These reactions are named Sandmeyer reactions. Although the mechanism of this reaction is complicated, as illustrated in Figure 1, they are believed to progress via an aryl copper...
2.4K
Diazonium Group Substitution: –OH and –H
3.3K
Nitrous acid, a weak acid, is prepared in situ via the reaction of sodium nitrite with a strong acid under cold conditions. This nitrous acid prepared in situ reacts with primary arylamines to form arenediazonium salts. Such reactions are known as diazotization reactions. As shown in Figure 1, the formation of arenediazonium salts begins with the decomposition of nitrous acid in an acidic solution to give nitrosonium ions.
3.3K
Structural Isomerism
21.4K
Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can...
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can...
21.4K
Valence Bond Theory
11.2K
Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
11.2K


