Photodissociation of organic molecules in star-forming regions II: Acetic acid

Details Photodissociation of organic molecules in star-forming regions II: Acetic acid Photodissociation of organic molecules in star-forming regions II: Acetic acid

2005-12-22

arxiv.org/abs/astro-ph/0512561v1

Astron.Astrophys. 449 (2006) 1289-1296

Astronomy and Astrophysics

Astrophysics

Comments: 8 pages, 5 figures, 3 tables. Accepted to be printed in A&A

Scientific paper

10.1051/0004-6361:20053927

Fragments from organic molecule dissociation (such as reactive ions and radicals) can form interstellar complex molecules like amino acids. The goal of this work is to experimentally study photoionization and photodissociation processes of acetic acid (CH$_3$COOH), a glycine (NH$_2$CH$_2$COOH) precursor molecule, by soft X-ray photons. The measurements were taken at the Brazilian Synchrotron Light Laboratory (LNLS), employing soft X-ray photons from a toroidal grating monochromator (TGM) beamline (100 - 310 eV). Mass spectra were obtained using the photoelectron photoion coincidence (PEPICO) method. Kinetic energy distribution and abundances for each ionic fragment have been obtained from the analysis of the corresponding peak shapes in the mass spectra. Absolute photoionization and photodissociation cross sections were also determined. We have found, among the channels leading to ionization, that only 4-6% of CH$_3$COOH survive the strong ionization field. CH$_3$CO$^+$, COOH$^+$ and CH$_3^+$ ions are the main fragments, and the presence of the former may indicate that the production-destruction process of acetic acid in hot molecular cores (HMCs) could decrease the H$_2$O abundance since the net result of this process converts H$_2$O into OH + H$^+$. The COOH$^+$ ion plays an important role in ion-molecule reactions to form large biomolecules like glycine.

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