Related Experiment Video
Updated: Aug 12, 2025
![[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
Photochemistry Driven by Excited-State Aromaticity Gain or Antiaromaticity Relief
Jiajie Yan1, Tomáš Slanina1,2, Joakim Bergman3
1Department of Chemistry-Ångström Laboratory, Uppsala University Box 523, 751 20, Uppsala, Sweden.
Abstract:
Gain of aromaticity or relief of antiaromaticity along a reaction path are important factors to consider in mechanism studies. Analysis of such changes along potential energy surfaces has historically focused on reactions in the electronic ground state (S0 ), but can also be used for excited states. In the lowest ππ* states, the electron counts for aromaticity and antiaromaticity follow Baird's rule where 4n π-electrons indicate aromaticity and 4n+2 π-electrons antiaromaticity. Yet, there are also cases where Hückel's rule plays a role in the excited state. The electron count reversals of Baird's rule compared to Hückel's rule explain many altered physicochemical properties upon excitation of (hetero)annulene derivatives. Here we illustrate how the gain of excited-state aromaticity (ESA) and relief of excited-state antiaromaticity (ESAA) have an impact on photoreactivity and photostability. Emphasis is placed on recent findings supported by the results of quantum chemical calculations, and photoreactions in a wide variety of areas are covered.
Related Concept Videos
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds
Photochemical Electrocyclic Reactions: Stereochemistry
Selection Rules: Photochemical Activation
Electrophilic Aromatic Substitution: Overview
Aromatic Hydrocarbon Anions: Structural Overview
Due to the absence of continuous...
Cycloaddition Reactions: MO Requirements for Photochemical Activation
ortho–para-Directing Activators: –CH3, –OH, –⁠NH2, –OCH3

![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)