Formation of methane and cyclohexane through the hydrogenation of toluene
arXiv:2508.13864 · doi:10.1051/0004-6361/202556920
Abstract
Methylated polycyclic aromatic hydrocarbons (PAHs) have been hypothesised to be present in the interstellar medium (ISM) through their 3.4 and 6.9 m absorption bands. To investigate the hydrogenation of these methylated PAHs, the simplest, toluene (), was exposed to H-atoms. This demonstrated how the presence of a methyl group changes the reactivity towards atomic hydrogen as compared to benzene and other PAHs and how this may alter its chemistry in the ISM. Toluene was deposited onto a graphite surface in an ultrahigh vacuum (UHV) chamber and then exposed to a H-atom beam. Temperature programmed desorption (TPD) measurements were used to investigate the reaction between H-atoms and toluene and the masses of hydrogenation products were measured with a quadrupole mass spectrometer (QMS). H-atom exposure of toluene leads to superhydrogenation of toluene and the formation of methyl-cyclohexane () at long exposure times. The initial cross-section of H-addition is lower than that of other PAHs. Methyl-cyclohexane can be further hydrogenated, leading to the detachment of the methyl group and production of cyclohexane () and methane (). Toluene may be fully hydrogenated through its interaction with H-atoms, although it has a smaller initial cross-section for H-atom addition compared to other PAHs. This likely reflects it having a smaller geometric cross-section and the low flexibility of the benzene ring when undergoing sp hybridization. The removal of the methyl group at high H-atom fluences provides a top down formation route to smaller molecules with the possibility of the formation of a radical cyclohexane combining with other species in an interstellar environment to form prebiotic molecules.
9 pages, 9 figures, 1 table, 2 appendix figures. Post peer-review and layout corrections. Accepted for publication in A&A
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