Tomographic reconstruction of photoelectron elliptical dichroism in chiral terpenes and terpenoids

Velocity-map imaging was combined with a novel tomographic reconstruction algorithm to investigate photoelectron elliptical dichroism (PEELD) in the 400 nm multiphoton ionization of the chiral molecules (+)-fenchone, (+)-α-pinene, and (+)-3-carene. Building on our recent study of the related species camphor [C. Sparling et al., J. Chem. Phys. 159, 214301 (2023)], we again find that cylindrical symmetry-breaking contributions to the photoelectron angular distributions play a non-negligible role. Furthermore, the angular structure of the PEELD response exhibits a more complex dependency on the ellipticity of the ionizing light than previously observed. Nevertheless, these features can be qualitatively rationalized using an extension of the simple two-basis-function model employed in our earlier work. Taken together, these results further underscore the value of efficient and robust tomographic approaches for interrogating PEELD phenomena across a range of different molecules.

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Publication Details

Journal
The Journal of Chemical Physics
Published
2026-08-18
DOI
https://doi.org/10.1063/5.0346143
Primary Topic
Laser-Matter Interactions and Applications
Type
article
Field-Weighted Citation Impact
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article

Tomographic reconstruction of photoelectron elliptical dichroism in chiral terpenes and terpenoids

Chris Sparling, Martin J. Paterson, Lewis Ireland, Dave Townsend et al.
The Journal of Chemical Physics
Laser-Matter Interactions and Applications
article

Tomographic reconstruction of photoelectron elliptical dichroism in chiral terpenes and terpenoids

Chris Sparling, Martin J. Paterson, Lewis Ireland, Dave Townsend, Ross Anderson, Justyna M. Żurek
article en

Abstract

Velocity-map imaging was combined with a novel tomographic reconstruction algorithm to investigate photoelectron elliptical dichroism (PEELD) in the 400 nm multiphoton ionization of the chiral molecules (+)-fenchone, (+)-α-pinene, and (+)-3-carene. Building on our recent study of the related species camphor [C. Sparling et al., J. Chem. Phys. 159, 214301 (2023)], we again find that cylindrical symmetry-breaking contributions to the photoelectron angular distributions play a non-negligible role. Furthermore, the angular structure of the PEELD response exhibits a more complex dependency on the ellipticity of the ionizing light than previously observed. Nevertheless, these features can be qualitatively rationalized using an extension of the simple two-basis-function model employed in our earlier work. Taken together, these results further underscore the value of efficient and robust tomographic approaches for interrogating PEELD phenomena across a range of different molecules.

The Journal of Chemical PhysicsVol. 165(7)
Heriot-Watt University (GB), Heriot-Watt University Malaysia (MY)
Openalex Percentile: Top 12%
Laser-Matter Interactions and Applications
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