Acyl Selenyl Sulfides as the Precursors for Reactive Sulfur Species (Hydrogen Sulfide, Polysulfide, and Selenyl Sulfide)
Akil Hamsath, Yingying Wang, Chuntao Yang, Shi Xu, Danica Cañedo, Wei Chen, Ming Xian
Abstract
Akil Hamsath, Yingying Wang, Chuntao Yang, Shi Xu, Danica Cañedo, Wei Chen, Ming Xian
Abstract
Persulfides are receiving increased attention due to their links to hydrogen sulfide (H 2 S) and hydrogen polysulfide (H 2 S n ). Their close analogues selenyl sulfides (RSeSHs), however, have limited literature precedent, and their reactivity and possible role in biology are largely unknown. Here, we devised an acyl selenyl sulfide template to study RSeSH chemistry. Their stability and reactivity toward amines/thiols were studied. These compounds can produce H 2 S or H 2 S 2 under different conditions, suggesting that RSeSHs are possible intermediates.
OpenAlex reports 17 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Persulfides are receiving increased attention due to their links to hydrogen sulfide (H 2 S) and hydrogen polysulfide (H 2 S n ). Their close analogues selenyl sulfides (RSeSHs), however, have limited literature precedent, and their reactivity and possible role in biology are largely unknown. Here, we devised an acyl selenyl sulfide template to study RSeSH chemistry. Their stability and reactivity toward amines/thiols were studied. These compounds can produce H 2 S or H 2 S 2 under different conditions, suggesting that RSeSHs are possible intermediates.
Key concepts: Polysulfide, Chemistry, Hydrogen sulfide, Reactivity (psychology), Sulfur, Sulfide, Hydrogen, Organic chemistry