Related Experiment Video
Updated: Apr 13, 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
Generating hydrated electrons through photoredox catalysis with 9-anthrolate
Christoph Kerzig1, Martin Goez
1Martin-Luther-Universität Halle-Wittenberg, Institut für Chemie, Kurt-Mothes-Str. 2, D-06120 Halle (Saale), Germany. martin.goez@chemie.uni-halle.de.
This study demonstrates a sustainable method for generating hydrated electrons using 9-anthrolate and ascorbate under near-UV light. The catalyst is regenerated, enabling efficient in situ production of these powerful reductants.
Area of Science:
- Photochemistry
- Physical Chemistry
- Chemical Kinetics
Background:
- Hydrated electrons are potent reductants with significant applications.
- Efficient and sustainable methods for their in situ generation are highly sought after.
Purpose of the Study:
- To develop a catalytic cycle for the in situ production of hydrated electrons.
- To utilize near-UV light (355 nm) for this process.
- To investigate the role of ascorbate as a sacrificial donor and catalyst regenerator.
Main Methods:
- Photoionization of 9-anthrolate in water using near-UV light.
- Employing ascorbate dianion as a sacrificial donor.
- Monitoring electron yields and catalyst regeneration through control experiments.
Main Results:
- A biphotonic photoionization pathway via the first excited singlet state of 9-anthrolate was identified.
- The anthroxy radical by-product is efficiently reduced by ascorbate dianion, regenerating the catalyst.
- Electron yields significantly exceeded catalyst concentration, confirming sustainable generation.
Conclusions:
- A catalytic cycle for sustainable in situ generation of hydrated electrons has been established.
- The process relies on efficient catalyst regeneration by the ascorbate dianion.
- This method offers a controlled and efficient route to produce powerful reductants.
Related Concept Videos
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Oxidation of Phenols to Quinones
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...
Redox Reactions
Redox Reactions
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
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...
Thermal and Photochemical Electrocyclic Reactions: Overview

