Contributions from Grain Surface and Gas Phase Chemistry to the Formation of Methyl Formate and Its Structural Isomers

Details Contributions from Grain Surface and Gas Phase Chemistry to the Formation of Methyl Formate and Its Structural Isomers Contributions from Grain Surface and Gas Phase Chemistry to the Formation of Methyl Formate and Its Structural Isomers

Feb 2011

adsabs.harvard.edu/cgi-bin/nph-data_query?bibcode=2011apj...728...71l&link_type=abstract

The Astrophysical Journal, Volume 728, Issue 1, article id. 71 (2011).

Astronomy and Astrophysics

Astronomy

9

Astrochemistry, Ism: Abundances, Ism: Clouds, Ism: Molecules

Scientific paper

Both grain surface and gas phase chemistry have been invoked to explain the disparate relative abundances of methyl formate and its structural isomers acetic acid and glycolaldehyde in the Sgr B2(N) star-forming region. While a network of grain surface chemistry involving radical-radical reactions during the warm-up phase of a hot core is the most chemically viable option proposed to date, neither qualitative nor quantitative agreement between modeling and observation has yet been obtained. In this study, we seek to test additional grain surface and gas phase processes to further investigate methyl formate-related chemistry by implementing several modifications to the Ohio State University gas/grain chemical network. We added two new gas phase chemical pathways leading to methyl formate, one involving an exothermic, barrierless reaction of protonated methanol with neutral formic acid; and one involving the reaction of protonated formic acid with neutral methanol to form both the cis and trans forms of protonated methyl formate. In addition to these gas phase processes, we have also investigated whether the relative product branching ratios for methanol photodissociation on grains influence the relative abundances of methyl formate and its structural isomers. We find that while the new gas phase formation pathways do not alter the relative abundances of methyl formate and its structural isomers, changes in the photodissociation branching ratios and adjustment of the overall timescale for warm-up can be used to explain their relative ratios in Sgr B2(N).

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