Double Photoionization of Nitrosyl Chloride by Synchrotron Radiation in the 24–70 eV Photon Energy Range

Author:

Schio Luca1ORCID,Alagia Michele1ORCID,Richter Robert2,Zhaunerchyk Vitali3,Stranges Stefano14ORCID,Pirani Fernando56ORCID,Vecchiocattivi Franco5ORCID,Parriani Marco5ORCID,Falcinelli Stefano5ORCID

Affiliation:

1. IOM CNR Laboratorio TASC, 34012 Trieste, Italy

2. Sincrotrone Trieste, Area Science Park, 34149 Trieste, Italy

3. Department of Physics, University of Gothenburg, 412 96 Gothenburg, Sweden

4. Department of Chemistry and Drug Technology, University of Rome Sapienza, 00185 Rome, Italy

5. Department of Civil and Environmental Engineering, University of Perugia, Via G. Duranti 93, 06125 Perugia, Italy

6. Department of Chemistry, Biology and Biotechnologies, University of Perugia, Via Elce di Sotto 8, 06123 Perugia, Italy

Abstract

The behavior of nitrosyl chloride (ClNO) exposed to ionizing radiation was studied by direct probing valence-shell electrons in temporal coincidence with ions originating from the fragmentation process of the transient ClNO2+. Such a molecular dication was produced by double photoionization with synchrotron radiation in the 24–70 eV photon energy range. The experiment has been conducted at the Elettra Synchrotron Facility of Basovizza (Trieste, Italy) using a light beam linearly polarized with the direction of the polarization vector parallel to the ClNO molecular beam axis. ClNO molecules crossing the photon beam at right angles in the scattering region are generated by effusive expansion and randomly oriented. The threshold energy for the double ionization of ClNO (30.1 ± 0.1 eV) and six dissociation channels producing NO+/Cl+, N+/Cl+, N+/O+, O+/Cl+, ClN+/O+, NO+/Cl2+ ion pairs, with their relative abundance and threshold energies, have been measured.

Funder

Italian MIUR

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

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