EGAS41 - Swansea University
EGAS41 - Swansea University
EGAS41 - Swansea University
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
41 st EGAS CP 92 Gdańsk 2009<br />
Mass-spectrometric studies of electron-impact dissociative<br />
ionization of glycine molecule<br />
V.S. Vukstich, A.I. Imre, O.A. Sitalo, A.V. Snegursky ∗<br />
Institute of Electron Physics, Ukrainian National Academy of Sciences, 21 Universitetska<br />
street, Uzhgorod 88017, Ukraine<br />
∗ Corresponding author: sneg@mail.uzhgorod.ua<br />
We have developed a mass-spectrometric apparatus based on the magnetic mass-analyzer<br />
intended for studying ionization of atoms and single/dissociative ionization of polyatomic<br />
molecules by low-energy electron impact. A primary emphasis was given to the production<br />
of ionic fragments following dissociation of complex molecules, mainly those having<br />
biological relevance. Such data are of specific interest in view of tracing the possible effects<br />
occurring in the live tissue under the influence of ionizing radiation accompanied by the<br />
production of slow secondary electrons, which, in turn, cause a series of structural transformations<br />
in the cells resulted in degradation of constituent elements of human/animal<br />
body [1]. Amino acids, which glycine belongs to, are one of the basic building blocks of<br />
the live body. Moreover, recent investigations have shown that amino acids are present<br />
in various space objects (say, meteorites and/or comets), proving, thus, the idea of life<br />
”import” to the Earth [2]. Of special interest is the fact that such molecules take an active<br />
part in constructing live cells and repairing damaged tissues, in particular, in forming<br />
antibodies, which fight against the viruses and bacteria that destroy the immune system<br />
of living organism. Experiment was carried out using a crossed-beam technique combined<br />
with mass separation of electron-molecule interaction products. The measuring procedure<br />
was fully automated using the PC control. Besides measuring the mass-spectra of<br />
the initial molecule, we have determined the energy dependences of the ionized fragment<br />
yield with the 0.3 eV energy step and the 0.2 − 0.5 eV (FWHM) energy resolution from<br />
the threshold up to 150 eV using a specially-designed electron gun instead of the conventional<br />
one used in the original version of mass-spectrometer ion source. It has been found<br />
that the main ionic fragments of the initial C 2 H 5 NO 2 molecule are CH 4 N + , CH 3 N + and<br />
CH 2 N + , which can be produced in various isomer states. Since the initial molecule may<br />
undergo strong fragmentation due to the thermal processes, special studies of possible<br />
temperature-induced fragmentation of the glycine molecule were carried out allowing one<br />
to choose the regime of molecular beam generation, minimizing, thus, the influence of<br />
thermal effects. Application of special least-square fitting procedure [3] enabled the absolute<br />
values of the appearance potentials for the above fragments to be found. Out data<br />
demonstrate fairly good agreement with the results of recent photoioniozation studies [4].<br />
More detailed analysis of experimental data and possible mechanisms of electron-impact<br />
glycine molecule fragmentation will be presented at the conference.<br />
References<br />
[1] B.D. Michael, P.A. O’Neill, Science 287, 1603 (2000)<br />
[2] Ed. A. Brack, The Molecular Origins of Life (Cambridge <strong>University</strong> press, Cambridge,<br />
UK, 1998)<br />
[3] G. Hanel, B. Gstir, T. Fiegele et al., J. Chem. Phys. 116, 2456 (2002)<br />
[4] H.-W. Jochims, M. Schwell, J-L. Chotin, J. Chem. Phys. 298, 279 (2004)<br />
152