Related Experiment Video
Updated: Jan 7, 2026
![[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F59739.jpg&w=3840&q=50)
[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst
Published on: May 21, 2019
Photosynthesis of Urea by Cooperative Radicals Addition Using a Peptide as a Photocatalyst
Yuanzhi Zhong1, Lihua Mo2, Xudan Chen1
1State Key Laboratory of Medicinal Chemical Biology, Key Laboratory of Bioactive Materials, Ministry of Education, College of Life Sciences, Nankai University, Tianjin, 300073, P.R. China.
Abstract:
Innovative strategies for efficient photocatalytic urea production are desirable due to the wide applications of urea and derivatives in agriculture and pharmaceuticals, which remain highly challenging. Here, we introduce a simple but efficient radical addition approach to address this challenge by fully utilizing the in situ, synchronously generated aminyl radical (·NH2) and hydroperoxyl radical (HO2·) via the coupling of photocatalytic NH3 oxidation and O2 reduction. The two radicals reassembled and cooperatively reacted with NH2COOH to form urea with markedly lower kinetic barrier than the industrial process. This approach not only achieved record-high urea production and conversion rates (42.6 mmol gcat -1 h-1 and 70%, respectively) but also enabled the direct, single-step synthesis of unsymmetrical urea derivatives with good yields.
Related Concept Videos
Cycloaddition Reactions: MO Requirements for Photochemical Activation
Urea Cycle
Radical Formation: Addition
Similar to charge conservation in chemical reactions, spin conservation is implicit for radical reactions. Accordingly, the product formed must possess an...
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Preparation of Amines: Reductive Amination of Aldehydes and Ketones
The Photochemical Reaction Center
![Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60786.jpg&w=3840&q=50)
