Abstract
Polycyclic aromatic hydrocarbons, (PAHs), constituted by benzene (C6H6) rings, as well as hydrogenated PAHs (Hn-PAHs), compounds with excess peripheral H atoms, emit infrared bands (3-12 μm) due to their vibrational transitions. These molecules are present in different astrophysical environments. For example, the band at 3.3μm, assigned to vibration of aromatic C-H bonds, is generally accompanied by the band at 3.4μm, assigned to vibration of aliphatic C-H bonds. The abundances of these molecules in circumstellar environments depend on the rates of formation and destruction by UV and X-rays radiation. We study experimentally the photoionization and photodissociation of the cyclohexane molecule (C6H12), a prototype Hn-PAH, using synchrotron radiation at UV (10-100 eV) and soft X-ray (280-310 eV) energies and the time-of-flight mass spectrometry. The measurements were performed at Brazilian National Light Synchrotron (LNLS) using the toroidal grating monochromator (TGM) beamline. From the mass spectra of ionic fragments produced by the interaction of photons with the molecule in gas phase, the production of each ion was quantified as a function of the photon energy. Moreover, the stability of C6H12 and C6H6 was analyzed by the identification of the produced ions. A greater production of ethyl (C2Hn+) and propyl (C4Hn+) ion groups was observed from the photodissociation of C6H12. We determined the photon flux as a function of the energy in the photodissociation region (PDR) of the planetary nebula NGC 7027, taking into account the attenuation caused by the H and the dust grains. From these photon flux values and the photoionization and photodissociation cross-sections, the ionization and destruction rates of C6H12 and C6H6 were determined. We concluded that the aromatic structure is more stable than the aliphatic structure against UV and X-ray radiation emitted by central star. Acknowledgments: CNPq, CAPES, LNLS.
