Gas-Phase
and Model Ice-Surface Reactions of S(<sup>1</sup>D) with Water and
Methanol: A Computational Investigation
and Implications for Cosmochemistry/Astrochemistry
posted on 2024-11-04, 16:26authored byAndrea Giustini, Gabriella Di Genova, Dimitrios Skouteris, Cecilia Ceccarelli, Marzio Rosi, Nadia Balucani
Gas-phase reactions of atomic sulfur in its first electronically
excited metastable state, S(<sup>1</sup>D), with water and methanol
have been theoretically investigated to characterize their potential
energy surfaces, the reaction mechanisms, and the product branching
fractions. According to our results, both reactions proceed with the
formation of bound intermediates that, for the isolated systems, decompose
into products because of the large energy content with which they
are formed. The SO(a <sup>1</sup>Δ) + H<sub>2</sub> channel
is the only open one for the S(<sup>1</sup>D) + H<sub>2</sub>O reaction,
while many channels are open for the S(<sup>1</sup>D) + CH<sub>3</sub>OH reaction. For the latter case, statistical estimates of the product
branching fractions indicate that the main channels are those leading
to CH<sub>2</sub>OH + SH, H<sub>2</sub>CO + H<sub>2</sub>S, H<sub>2</sub>CS + H<sub>2</sub>O, and CH<sub>3</sub> + HSO. The mechanism
of the related O(<sup>1</sup>D) + CH<sub>3</sub>SH reaction has also
been unveiled. Since the reaction intermediates can be stabilized
by energy loss to surrounding species on ice or in liquid water, to
gain some insights into the possible effects of water molecules, we
have also analyzed how the two reactions behave when four additional
water molecules are added. The conclusion is that the initial intermediates
formed by the insertion or addition mechanism, namely, HOSH (hydrogen
thioperoxide) and H<sub>2</sub>OS for S(<sup>1</sup>D) + H<sub>2</sub>O and CH<sub>2</sub>OHSH (mercaptomethanol), CH<sub>4</sub>OS and
CH<sub>3</sub>OSH (methyl thioperoxide) for S(<sup>1</sup>D) + CH<sub>3</sub>OH, as well as CH<sub>3</sub>SOH (methyl sulfenic acid) for
O(<sup>1</sup>D) + CH<sub>3</sub>SH, will probably be stabilized by
the interaction with the additional water molecules. Our results can
help in understanding sulfur chemistry in space, especially in the
case of comets. On the one hand, the S(<sup>1</sup>D) + H<sub>2</sub>O gas-phase reaction could account for the additional SO source necessary
to explain the observed distribution of this species obtained by using
the Plateau de Bure interferometer of Institut de Radioastronomie
Millimétrique (IRAM) for the Hale Bopp comet. On the other
hand, some of the S/O-containing molecules identified by ROSINA (Rosetta
Orbiter Spectrometer for Ion and Neutral Analysis) during the enhanced
dust emission events of the 67/P comet (e.g., species with the gross
formula HSO, H<sub>2</sub>SO, and CH<sub>4</sub>OS) could be the results
of the chemistry occurring on ice that we have exposed in this work.