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Delayed fragmentation of isolated nucleobases induced by MeV ions.
Nakao, T; Takasu, R; Tsuchida, H; Saito, M; Majima, T.
Afiliação
  • Nakao T; Department of Nuclear Engineering, Kyoto University, Kyoto 615-8540, Japan.
  • Takasu R; Department of Nuclear Engineering, Kyoto University, Kyoto 615-8540, Japan.
  • Tsuchida H; Department of Nuclear Engineering, Kyoto University, Kyoto 615-8540, Japan.
  • Saito M; Quantum Science and Engineering Center, Kyoto University, Uji 611-0011, Japan.
  • Majima T; Department of Nuclear Engineering, Kyoto University, Kyoto 615-8540, Japan.
J Chem Phys ; 161(5)2024 Aug 07.
Article em En | MEDLINE | ID: mdl-39087542
ABSTRACT
We evaluated the dissociation of isolated gas-phase nucleobase molecules induced by mega electron volt (MeV)-energy ions to gain fundamental insights into the reactions of nucleobases upon fast ion irradiation. We studied five nucleobase molecules-adenine, guanine, cytosine, thymine, and uracil-as gas-phase targets. We compared the fragmentation patterns obtained from carbon ion impacts with those obtained from proton impacts to clarify the effect of heavy ion irradiation. We also compared the results with electron impact and photoionization results. In addition, we identified several delayed fragmentation pathways by analyzing the correlation between fragment pairs generated from singly and doubly charged intermediate ions. To determine the lifetimes of delayed fragmentation from singly charged intermediate ions, we evaluated the detection efficiencies of the microchannel plate detector for the neutral fragment HCN as a function of kinetic energy using a new methodology. As the first demonstration of this method, we estimated the lifetimes of C5H5N5+ generated by 1.2-MeV C+ and 0.5-MeV H+ collisions to be 0.87 ± 0.43 and 0.67 ± 0.09 µs, respectively. These lifetimes were approximately one order of magnitude longer than those of the doubly charged intermediate ion C5H5N52+.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article