绿色化学的聚光灯:由硫酸盐介导的无金属有机转化
Rapelly Venkatesh1, Priyanka Chaudhary2
1Institute of Chemistry, Academia Sinica Taipei 115201 Taiwan.
RSC advances
|November 10, 2025
概括
硫酸盐 (K2S2O8) 是一种绿色氧化剂,用于C-C和C-原子键的无金属合成. 本综述强调了最近对K2S2O8促进的氧化转换的进展和机制性见解.
科学领域:
- 有机化学 有机化学
- 绿色化学 绿色化学
- 合成方法论 合成方法论
背景情况:
- 硫酸盐 (K2S2O8) 是一种廉价的氧化剂.
- 它促进了无金属的氧化转化.
- K2S2O8被认为是化学合成中的绿色替代品.
研究的目的:
- 审查K2S2O8在有机合成中的最新应用 (2018-2024年).
- 为了突出无金属氧化反应的进步.
- 确定研究缺口,并鼓励新的K2S2O8推广的方法.
主要方法:
- 关于K2S2O8在有机转化中的应用的文献综述.
- 对无金属反应的关键进展进行分析.
- 详细检查反应机制,重点关注自由基路径.
主要成果:
- 总结了K2S2O8在形成C-C和C-异原子键中的作用.
- 确定了无金属氧化合反应的关键进展.
- 提供了对K2S2O8介导的激进过程的机械洞察力.
结论:
- K2S2O8是一种用于绿色氧化转换的多功能试剂.
- 进一步的研究可以利用K2S2O8用于新的合成策略.
- 了解反应机制对于开发新方法至关重要.
相关概念视频
Oxidation of Alkenes: Syn Dihydroxylation with Potassium Permanganate
16.3K
Alkenes can be dihydroxylated using potassium permanganate. The method encompasses the reaction of an alkene with a cold, dilute solution of potassium permanganate under basic conditions to form a cis-diol along with a brown precipitate of manganese dioxide.
16.3K
Electrophilic Aromatic Substitution: Sulfonation of Benzene
7.7K
Sulfonation of benzene is a reaction wherein benzene is treated with fuming sulfuric acid at room temperature to produce benzenesulfonic acid. Fuming sulfuric acid is a mixture of sulfur trioxide and concentrated sulfuric acid.
7.7K
Oxidation and Reduction of Organic Molecules
9.1K
Energy production within a cell involves many coordinated chemical pathways. Most of these pathways are combinations of oxidation and reduction reactions, which occur at the same time. An oxidation reaction strips an electron from an atom in a compound, and the addition of this electron to another compound is a reduction reaction. Because oxidation and reduction usually occur together, these pairs of reactions are called redox reactions.
The removal of an electron from a molecule, results in a...
The removal of an electron from a molecule, results in a...
9.1K
Oxidation of Alcohols
15.6K
In this lesson, the oxidation of alcohols is discussed in depth. The various reagents used for oxidation of primary and secondary alcohols are detailed, and their mechanism of action is provided.
The process of oxidation in a chemical reaction is observed in any of the three forms:
The process of oxidation in a chemical reaction is observed in any of the three forms:
15.6K
Preparation and Reactions of Sulfides
5.7K
Sulfides are the sulfur analog of ethers, just as thiols are the sulfur analog of alcohol. Like ethers, sulfides also consist of two hydrocarbon groups bonded to the central sulfur atom. Depending upon the type of groups present, sulfides can be symmetrical or asymmetrical. Symmetrical sulfides can be prepared via an SN2 reaction between 2 equivalents of an alkyl halide and one equivalent of sodium sulfide.
5.7K
Preparation and Reactions of Thiols
7.4K
Thiols are prepared using the hydrosulfide anion as a nucleophile in a nucleophilic substitution reaction with alkyl halides. For instance, bromobutane reacts with sodium hydrosulfide to give butanethiol.
7.4K


