The formation pathways to silicon- and sulfur-containing molecules are crucial to the understanding of silicon-sulfur chemistry in interstellar and circumstellar environments. While multiple silicon- and sulfur-containing species have been observed in deep space, their fundamental formation mechanisms are largely unknown. The crossed molecular beams technique combined with electronic structure and Rice-Ramsperger-Kassel-Marcus (RRKM) calculations was utilized to study the bimolecular reaction of atomic silicon (Si(P)) with thiomethanol (CHSH, XA') leading to the thiosilaformyl radical (HSiS, XA') via an exclusive methyl radical (CH, XA″) loss via indirect scattering dynamics which involves barrierless addition and hydrogen migration in an overall exoergic reaction, indicating the possibility that HSiS can form in cold molecular clouds. The astronomically elusive thiosilaformyl radical may act as a tracer of an exotic silicon-sulfur chemistry to be deciphered toward, for example, the star-forming region SgrB2, thus leading to a better understanding of the formation of silicon-sulfur bonds in deep space.
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http://dx.doi.org/10.1021/acs.jpclett.1c01706 | DOI Listing |
J Phys Chem Lett
July 2021
Department of Chemistry, University of Hawai'i at Ma̅noa, Honolulu, Hawaii 96822, United States.
The formation pathways to silicon- and sulfur-containing molecules are crucial to the understanding of silicon-sulfur chemistry in interstellar and circumstellar environments. While multiple silicon- and sulfur-containing species have been observed in deep space, their fundamental formation mechanisms are largely unknown. The crossed molecular beams technique combined with electronic structure and Rice-Ramsperger-Kassel-Marcus (RRKM) calculations was utilized to study the bimolecular reaction of atomic silicon (Si(P)) with thiomethanol (CHSH, XA') leading to the thiosilaformyl radical (HSiS, XA') via an exclusive methyl radical (CH, XA″) loss via indirect scattering dynamics which involves barrierless addition and hydrogen migration in an overall exoergic reaction, indicating the possibility that HSiS can form in cold molecular clouds.
View Article and Find Full Text PDFPhys Chem Chem Phys
June 2021
School of Maths and Physics, Queen's University Belfast, University Road, Belfast BT7 1NN, Northern Ireland, UK.
The reactions of the D1-silylidyne radical (SiD; X2Π) with deuterium sulfide (D2S; X1A1) and hydrogen sulfide (H2S; X1A1) were conducted utilizing a crossed molecular beams machine under single collision conditions. The experimental work was carried out in conjunction with electronic structure calculations. The elementary reaction commences with a barrierless addition of the D1-silylidyne radical to one of the non-bonding electron pairs of the sulfur atom of hydrogen (deuterium) sulfide followed by possible bond rotation isomerization and multiple atomic hydrogen (deuterium) migrations.
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