Methoxymethanol formation starting from CO hydrogenation

Abstract

Context. Methoxymethanol (CH3OCH2OH) has been identified through gas-phase signatures in both high- and low-mass star-forming regions. Like several other C-, O-, and H-containing complex organic molecules (COMs), this molecule is expected to form upon hydrogen addition and abstraction reactions in CO-rich ice through radical recombination of CO hydrogenation products. Aims. The goal of this work is to experimentally and theoretically investigate the most likely solid-state methoxymethanol reaction channel athe recombination of CH2OH and CH3O radicals afor dark interstellar cloud conditions and to compare the formation efficiency with that of other species that were shown to form along the CO-hydrogenation line. We also investigate an alternative hydrogenation channel starting from methyl formate. Methods. Hydrogen atoms and CO or H2CO molecules were co-deposited on top of predeposited H2O ice to mimic the conditions associated with the beginning of arapida CO freeze-out. The formation of simple species was monitored in situ using infrared spectroscopy. Quadrupole mass spectrometry was used to analyze the gas-phase COM composition following a temperature-programmed desorption. Monte Carlo simulations were used for an astrochemical model comparing the methoxymethanol formation efficiency with that of other COMs. Results. The laboratory identification of methoxymethanol is found to be challenging, in part because of diagnostic limitations, but possibly also because of low formation efficiencies. Nevertheless, unambiguous detection of newly formed methoxymethanol has been possible in both CO+H and H2CO+H experiments. The resulting abundance of methoxymethanol with respect to CH3OH is about 0.05, which is about six times lower than the value observed toward NGC 6334I and about three times lower than the value reported for IRAS 16293B. Astrochemical simulations predict a similar value for the methoxymethanol abundance with respect to CH3OH, with values ranging between 0.03 and 0.06. Conclusions. We find that methoxymethanol is formed by co-deposition of CO and H2CO with H atoms through the recombination of CH2OH and CH3O radicals. In both the experimental and modeling studies, it is found that the efficiency of this channel alone is not sufficient to explain the observed abundance of methoxymethanol with respect to methanol. The rate of a proposed alternative channel, the direct hydrogenation of methyl formate, is found to be even less efficient. These results suggest that our knowledge of the reaction network is incomplete or involving alternative solid-state or gas-phase formation mechanisms. ©