有机氧化物UV光解离动力学:实验和理论
Meijun Zou1, Emmanuel Moya Cruz1, Christopher A Sojdak1
1Department of Chemistry, University of Pennsylvania, Philadelphia, Pennsylvania 19104-6323, United States.
The journal of physical chemistry. A
|March 20, 2025
概括
紫外线可以将有机氧化物 (ROOH) 分解为基. 这项研究揭示了OH基是如何形成的,影响大气化学和氧化循环.
科学领域:
- 摄影化学的使用.
- 大气化学 大气化学
- 化学动力学 化学动力学
背景情况:
- 有机氧化物 (ROOH) 是大气氧化过程中的关键中间体.
- 了解它们的紫外线光解离对于大气模型至关重要.
研究的目的:
- 为了研究三个代表性的有机氧化的紫外线光解离动力学.
- 阐明 (OH) 基产物的形成路径和反弹动力学.
主要方法:
- 实验:从282nm光解离中获得OH产物的速度图像成像.
- 理论:用于ROOH解离的放松潜在能量表面的计算.
- 分析:检查释放的总动能 (TKER) 和角分布.
主要成果:
- 观察到双模态TKER分布,表明多个解离路径.
- OH产物的同位素角分布,与直接光解离预测相反.
- 理论计算支持由于低扭矩障碍,OH在不同方向上的反弹.
结论:
- 光解离包括直接解离和内部转换到基本状态.
- 基团几何变化影响解离产物的能量分布.
- 为 OH 基再生的大气模型提供关键数据.
相关概念视频
Autoxidation of Ethers to Peroxides and Hydroperoxides
Ethers represent a class of chemical compounds that become more dangerous with prolonged storage because they tend to form explosive peroxides when standing in the air. Autoxidation is the spontaneous oxidation of a compound in air. In the presence of oxygen, ethers slowly oxidize to form hydroperoxides and dialkyl peroxides.
Regioselectivity of Electrophilic Additions-Peroxide Effect
In the presence of organic peroxides, the addition of hydrogen bromide to an alkene yields the isomer that is not predicted by Markovnikov’s rule. For example, the addition of hydrogen bromide to 2-methylpropene in the presence of peroxides gives 1-bromo-2-methylpropane. This addition reaction proceeds via a free radical mechanism, which reverses the regioselectivity. The free radical reaction mechanism involves three stages: initiation, propagation, and termination.
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
Diols are compounds with two hydroxyl groups. In addition to syn dihydroxylation, diols can also be synthesized through the process of anti dihydroxylation. The process involves treating an alkene with a peroxycarboxylic acid to form an epoxide. Epoxides are highly strained three-membered rings with oxygen and two carbons occupying the corners of an equilateral triangle. This step is followed by ring-opening of the epoxide in the presence of an aqueous acid to give a trans diol.
Preparation of Epoxides
Overview
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...
Photochemical Electrocyclic Reactions: Stereochemistry
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
Radical Autoxidation
The oxidation of an organic compound in the presence of air or oxygen is called autoxidation. For example, cumene reacts with oxygen to form hydroperoxide. Autoxidation involves initiation, propagation, and termination steps. Many organic compounds are susceptible to autoxidation—especially ethers in the presence of oxygen, which form hydroperoxides. Even though this reaction is slow, old ether bottles contain small amounts of peroxide, which leads to laboratory explosions during ether...


