Related Experiment Video
Updated: Jul 11, 2026

Developing Photosensitizer-Cobaloxime Hybrids for Solar-Driven H2 Production in Aqueous Aerobic Conditions
Published on: October 5, 2019
A photochemical mechanism for homochirogenesis
Richard M Pagni1, John Bartmess
1Department of Chemistry, University of Tennessee, Knoxville, Tennessee 37996-1600, USA.
Abstract:
Theoretical analysis of one-step and multiple-step photoreactions initiated with circularly polarized light shows that the enantiomeric excess of a chiral reactant approaches +/- 1 as the amount of unreacted reactant approaches 0. The final product never has a large enantiomeric excess at any stage of its formation and slowly decreases to 0 at the completion of the reaction. For multiple-step reactions the behavior of the intermediate photoproducts is much more interesting. During certain stages of the overall reaction both the size of the enantiomer excess and the amount of a given intermediate photoproduct are large. Furthermore, the sign of the enantiomeric excess of an intermediate may change during the course of the reaction. Multiple-step photoreactions initiated with circularly polarized light may be a method by which the exogenous and endogenous synthesis of optically active molecules occurred in the prebiotic universe.
Related Concept Videos
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Cycloaddition Reactions: MO Requirements for Photochemical Activation
The Z-Scheme of Electron Transport in Photosynthesis
The Photochemical Reaction Center
Photosystem II
The pigment molecules are arranged across two photosystem domains — the antenna complex and the reaction center. The main aim of the pigment molecules...
Radical Formation: Homolysis
