: We report the x-ray absorption spectrum (XAS) of the tert-butyl radical, C4H9. The radical was generated pyrolytically from azo-tert-butane, and the XAS of the pure radical was obtained by subtraction of spectra recorded at different temperatures. The bands in the XAS were assigned by ab initio calculations that are in very good agreement with the experimental data. The lowest energy signal in the XAS is assigned to the C1s electron transition from the central carbon atom to the singly occupied molecular orbital (SOMO), while higher transitions correspond to C1s excitations from terminal carbon atoms. Furthermore, we investigated the fragmentation of the radical following resonant C1s excitation by electron-ion-coincidence spectroscopy. Several fragmentation channels were identified. The C1s excitation of the terminal carbons is associated with a stronger fragmentation tendency compared to the lowest C1s excitation of the central carbon into the SOMO. For this core excited state, we still observe an intact parent ion, C4H9+, and a comparatively higher tendency to dissociate into CH3+ + C3H6+.

The x-ray absorption spectrum of the tert-butyl radical: An experimental and computational investigation

Michele Alagia;Stefano Stranges;
2024

Abstract

: We report the x-ray absorption spectrum (XAS) of the tert-butyl radical, C4H9. The radical was generated pyrolytically from azo-tert-butane, and the XAS of the pure radical was obtained by subtraction of spectra recorded at different temperatures. The bands in the XAS were assigned by ab initio calculations that are in very good agreement with the experimental data. The lowest energy signal in the XAS is assigned to the C1s electron transition from the central carbon atom to the singly occupied molecular orbital (SOMO), while higher transitions correspond to C1s excitations from terminal carbon atoms. Furthermore, we investigated the fragmentation of the radical following resonant C1s excitation by electron-ion-coincidence spectroscopy. Several fragmentation channels were identified. The C1s excitation of the terminal carbons is associated with a stronger fragmentation tendency compared to the lowest C1s excitation of the central carbon into the SOMO. For this core excited state, we still observe an intact parent ion, C4H9+, and a comparatively higher tendency to dissociate into CH3+ + C3H6+.
2024
Istituto Officina dei Materiali - IOM -
x-ray, nexafs, radicals, frozen-core core–valence, Natural Transition Orbitals
File in questo prodotto:
File Dimensione Formato  
The X-ray absorption spectrum of the tert-butyl radical_AIP2024.pdf

Open Access dal 18/12/2025

Descrizione: This article may be downloaded for personal use only. Any other use requires prior permission of the author and AIP Publishing. This article appeared in Dorothee Schaffner, Theo Juncker von Buchwald, Emil Karaev, Michele Alagia, Robert Richter, Stefano Stranges, Sonia Coriani, Ingo Fischer; The x-ray absorption spectrum of the tert-butyl radical: An experimental and computational investigation. J. Chem. Phys. 21 July 2024; 161 (3): 034309 and may be found at https://doi.org/10.1063/5.0216364
Tipologia: Versione Editoriale (PDF)
Licenza: Altro tipo di licenza
Dimensione 4.35 MB
Formato Adobe PDF
4.35 MB Adobe PDF Visualizza/Apri
2024_t-butyl-Accepted_JCP24-AR-01820.pdf

accesso aperto

Descrizione: This article may be downloaded for personal use only. Any other use requires prior permission of the author and AIP Publishing. This article appeared in Dorothee Schaffner, Theo Juncker von Buchwald, Emil Karaev, Michele Alagia, Robert Richter, Stefano Stranges, Sonia Coriani, Ingo Fischer; The x-ray absorption spectrum of the tert-butyl radical: An experimental and computational investigation. J. Chem. Phys. 21 July 2024; 161 (3): 034309 and may be found at https://doi.org/10.1063/5.0216364
Tipologia: Documento in Post-print
Licenza: Altro tipo di licenza
Dimensione 1.85 MB
Formato Adobe PDF
1.85 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/487381
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 2
  • ???jsp.display-item.citation.isi??? 2
social impact