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Tilmann D. Märk

Researcher at University of Innsbruck

Publications -  668
Citations -  19726

Tilmann D. Märk is an academic researcher from University of Innsbruck. The author has contributed to research in topics: Ion & Electron ionization. The author has an hindex of 64, co-authored 662 publications receiving 18712 citations. Previous affiliations of Tilmann D. Märk include University of New Hampshire & Claude Bernard University Lyon 1.

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Journal ArticleDOI

Dissociative electron attachment to nitroaromatic compounds – resonances as fingerprints for isomers

TL;DR: In this article, the authors present detailed free electron attachment measurements on nitroaromatic compounds in the gas phase and show that dissociative electron attachment can act as a selective and sensitive probe for the identification of isomeric forms of nitrotoluene and dinitrobenzene.
Journal ArticleDOI

Some investigations of the ignition and development of breakdown in cylindrical hollow cathode glow discharges

TL;DR: In this article, the breakdown behavior of hollow cathode glow discharge was investigated in a cylindrical, hollow cathodes structure having an internal diameter of 2 cm, where the anode is a plane electrode across one end of the cathode cylinder.
Journal ArticleDOI

Electron transfer processes in binary van der Waals clusters via the N2−(2Πg) resonance

TL;DR: In this paper, free electron attachment in the energy range 0-4 eV to binary van der Waals clusters composed of N2/SF6 and O2/O2 is studied with high resolution (< 0.1 eV).
Book ChapterDOI

Spontaneous Decay of Ionized Atomic Clusters: Statistical and Non-Statistical Channels

TL;DR: In this paper, the authors describe the formation of hot ions, i.e., the deposition of excess energy into various degrees of freedom, which leads to spontaneous decay reactions of these hot ions on time scales ranging from a few vibrational oscillations for prompt dissociations up to several 100 µs for metastable dissociation.
Proceedings ArticleDOI

Dissociative Electron Attachment to Thymine: Bond and Site Selectivity in Different Molecular Environments

TL;DR: Experiments with partially deuterated or methylated thymine show that the site of dehydrogenation can be precisely controlled by the incident electron energy, and such bond and site selectivity remains in more complex environments when thymine is a moiety of thymidine (base+sugar unit) and of a thymine cluster embedded in a superfluid helium droplet.