Zobrazeno 1 - 10
of 278
pro vyhledávání: '"Eugen, Illenberger"'
Autor:
Rebecca Meißner, Jaroslav Kočišek, Linda Feketeová, Juraj Fedor, Michal Fárník, Paulo Limão-Vieira, Eugen Illenberger, Stephan Denifl
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-7 (2019)
Radiosensitisers are believed to interfere with cancer cells by dissociating upon interaction with electrons. Here the authors observe instead that the dominant path for nitroimidazolic radiosensitisers involves formation of a non-dissociated radical
Externí odkaz:
https://doaj.org/article/cd9cad2156bb416a9e119dc7b675e27c
Publikováno v:
Int.J.Mol.Sc.
Int.J.Mol.Sc., 2019, 20 (14), pp.3496. ⟨10.3390/ijms20143496⟩
International Journal of Molecular Sciences, Vol 20, Iss 14, p 3496 (2019)
International Journal of Molecular Sciences
Volume 20
Issue 14
Int.J.Mol.Sc., 2019, 20 (14), pp.3496. ⟨10.3390/ijms20143496⟩
International Journal of Molecular Sciences, Vol 20, Iss 14, p 3496 (2019)
International Journal of Molecular Sciences
Volume 20
Issue 14
Misonidazole (MISO) was considered as radiosensitizer for the treatment of hypoxic tumors. A prerequisite for entering a hypoxic cell is reduction of the drug, which may occur in the early physical-chemical stage of radiation damage. Here we study el
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7797512877b8343e56f5c3b02c1adc50
https://hal.archives-ouvertes.fr/hal-02277850
https://hal.archives-ouvertes.fr/hal-02277850
Publikováno v:
J.Phys.Chem.C
J.Phys.Chem.C, 2018, 122 (42), pp.24137-24142. ⟨10.1021/acs.jpcc.8b07377⟩
J.Phys.Chem.C, 2018, 122 (42), pp.24137-24142. ⟨10.1021/acs.jpcc.8b07377⟩
International audience; One of the major challenges in chemical synthesis is to trigger and control a specific reaction route leading to a specific final product, while side products are avoided. Methodologies based on resonant processes at the molec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::089251f3620082802dd2abae9a7938b3
https://hal.archives-ouvertes.fr/hal-01909209
https://hal.archives-ouvertes.fr/hal-01909209
Autor:
Eugen Illenberger, Martina C. Meinke
Publikováno v:
International Journal of Mass Spectrometry. :80-85
Dissociative electron attachment (DEA) to acetone (CH3COCH3), perfluoroacetone (CF3COCF3) and acetylene (HCCH) is studied in the gas phase under collision-free conditions. The results are compared with those recently obtained from a study on electron
Autor:
Eugen Illenberger, Janina Kopyra
Publikováno v:
International Journal of Mass Spectrometry. :98-105
Relative cross sections obtained in dissociative electron attachment (DEA) reactions from crossed beams experiment are often normalised using absolute rate coefficients obtained from electron swarm experiments. Both methods, however, are carried out
Publikováno v:
Chemical Physics Letters. 578:54-58
Dissociative electron attachment (DEA) to the simplest hetero dipeptide (alanyl-glycine) is studied by means of a beam experiment. The results are compared with those previously obtained from the single compounds alanine and glycine from which the di
Autor:
Christian Mitterdorfer, Paul Scheier, Katrin Tanzer, Eugen Illenberger, S. Karolczak, Peter Bartl, Stephan Denifl
Publikováno v:
Rapid Communications in Mass Spectrometry. 27:298-304
RATIONALE Electron ionization of three perfluoroethers (PFEs), C6F14O3, C8F18O4, and C10F20O5, is studied in the gas phase and when the molecules are embedded in ultracold helium (He) droplets. The molecules investigated are model compounds for perfl
Publikováno v:
Chemical Physics Letters. 550:47-51
Dissociative electron attachment (DEA) to N -acetylglycine has been studied in the gas phase by means of a crossed beams apparatus. In this Letter we present the results obtained from the target molecule and compare these with the results from its co
Publikováno v:
International Journal of Mass Spectrometry. :95-99
Dissociative electron attachment (DEA) to perfluorohexane (C 6 F 14 ), perfluoro(methylcyclo-hexane) (C 6 F 11 CF 3 ) and perfluorocyclohexanecarbonyl chloride (C 6 F 11 C(O)Cl) is studied in a crossed electron-molecular beam experiment with mass spe
Publikováno v:
International Journal of Mass Spectrometry. 315:40-45
The formation of negative ions following low energy (0–12 eV) electron attachment to the title compounds is studied in a crossed electron-molecular beam experiment applying mass spectrometric detection of the anions. All silane derivatives presentl