用于非水性还原电合成的子介导极
Jack Twilton1, Mathew R Johnson1, Vinayak Sidana1
1Department of Chemistry, University of Wisconsin-Madison, Madison, WI, USA.
Nature
|August 21, 2023
概括
一个新的介导 (H2) 阳极通过间接电化学氧化H2来实现可持续的电合成减少. 这项技术支持催化交叉电友合反应,促进更绿色的化学合成.
科学领域:
- 绿色化学
- 电化学
- 有机合成
背景情况:
- 电化学合成为工业化学品提供了可持续的途径.
- 电合成减少通常需要外部电子源,通常依赖于牺牲阳极.
- 阳极水氧化具有吸引力,但由于无水反应条件的要求而受到限制,突出显示了像H2这样的替代减少剂来源的需要.
研究的目的:
- 在非水性条件下开发可持续的中介阳极.
- 用介质使H2的间接电化学氧化成为可能.
- 将这项技术应用于具有挑战性的反应,例如催化交叉电友合 (XEC).
主要方法:
- 通过将 antraquinone 中介的热催化化与 anthrahydroquinone 的电化学氧化结合而开发出一个介导的 H2 阳极.
- 介导阳极用于支持催化交叉电友合 (XEC) 反应.
- 该方法在小规模批量反应中得到验证,并在循环流反应器中扩大规模.
主要成果:
- 介导的H2阳极成功支持催化XEC反应.
- 使用循环流反应器实现了制药中间体的度合成.
- 开发的技术为H2驱动的电合成减少提供了总体策略.
结论:
- 介导H2阳极技术为电合成减少提供了牺牲阳极的可持续替代方案.
- 这种方法促进了更环保的化学制造,特别是在制药行业.
- 该系统可适应小规模验证和大规模合成.
相关概念视频
Anoxygenic Photosynthesis
50
Anoxygenic photosynthesis is a phototrophic process that captures light energy to drive carbon fixation without producing molecular oxygen. Unlike oxygenic photosynthesis, which utilizes water as an electron donor and releases oxygen, anoxygenic phototrophs use alternative electron donors such as hydrogen sulfide (H₂S), elemental sulfur (S⁰), or thiosulfate (S₂O₃²⁻). This process is carried out by diverse groups of bacteria, including purple bacteria, green...
50
The Z-Scheme of Electron Transport in Photosynthesis
10.2K
The light reactions of photosynthesis assume a linear flow of electrons from water to NADP+. During this process, light energy drives the splitting of water molecules to produce oxygen. However, oxidation of water molecules is a thermodynamically unfavorable reaction and requires a strong oxidizing agent. This is accomplished by the first product of light reactions: oxidized P680 (or P680+), the most powerful oxidizing agent known in biology. The oxidized P680 that acquires an electron from the...
10.2K
Oxidation of Phenols to Quinones
3.1K
In the presence of oxidizing agents, phenols are oxidized to quinones. Quinones can be easily reduced back to phenols using mild reducing agents. The electron-donating hydroxyl group enhances the reactivity of the aromatic ring, enabling oxidation of the ring even in the absence of an α hydrogen.
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox...
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox...
3.1K
Electrolysis
26.6K
In a galvanic cell, the electrical work is done by a redox system on its surroundings as electrons produced by the spontaneous redox reactions are transferred through an external circuit. Alternatively, an external circuit does work on a redox system by imposing a voltage sufficient to drive an otherwise nonspontaneous reaction in a process known as electrolysis. For instance, recharging a battery involves the use of an external power source to drive the spontaneous (discharge) cell reaction in...
26.6K
Voltaic/Galvanic Cells
57.5K
Spontaneous Chemical Reactions
Spontaneous redox reactions occur abundantly in nature. The chemical reaction occurring in a disposable AA battery powering our remote controls is one such example of a spontaneous redox reaction. Another example is the immersion of coiled copper wire into an aqueous silver nitrate solution. The reaction shows a gradual, visually impressive color change from colorless to bright blue and the formation of a grey precipitate on the copper wire. In this experiment,...
Spontaneous redox reactions occur abundantly in nature. The chemical reaction occurring in a disposable AA battery powering our remote controls is one such example of a spontaneous redox reaction. Another example is the immersion of coiled copper wire into an aqueous silver nitrate solution. The reaction shows a gradual, visually impressive color change from colorless to bright blue and the formation of a grey precipitate on the copper wire. In this experiment,...
57.5K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
3.4K
Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
3.4K


![Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F55858.jpg&w=3840&q=50)