Carotenoid radical formation after multi-photon excitation of 8′-apo-β-carotenal

Abstract

Carotenoids containing a conjugated C[double bond, length as m-dash]O group exhibit complex excited-state dynamics that are influenced by solvent polarity due to the involvement of an intramolecular charge transfer (ICT) state. Our study explores the excited-state behavior of 8′-apo-β-carotenal under multi-photon excitation conditions. Using near-infrared (1300 nm) multi-photon excitation, we observe the formation of a cation radical of 8′-apo-β-carotenal, a process distinct from those following one-photon visible or UV excitation. Our findings suggest that this radical formation results from multi-photon excitation involving a higher-lying dark state, supported by intensity-dependent experiments. This work demonstrates that radical generation is a characteristic of this higher excited state and is not produced during relaxation from the S1/ICT state. The results open new pathways for understanding carotenoid radical formation mechanisms under intense multi-photon excitation.

Graphical abstract: Carotenoid radical formation after multi-photon excitation of 8′-apo-β-carotenal

Supplementary files

Article information

Article type
Paper
Submitted
16 Nov 2024
Accepted
16 Feb 2025
First published
17 Feb 2025

Phys. Chem. Chem. Phys., 2025, Advance Article

Carotenoid radical formation after multi-photon excitation of 8′-apo-β-carotenal

V. Šebelík, V. Kuznetsova, I. Šímová and T. Polívka, Phys. Chem. Chem. Phys., 2025, Advance Article , DOI: 10.1039/D4CP04373A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements