ArticleNature chemistry2026
Spontaneous trisulfide metathesis in polar aprotic solvents.
Article in Nature chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
2 citing papers in PubMed.
- A poly(trisulfide) oligomer with antimicrobial activity.Chemical science · 2026Article
- Kinetically Enhanced Access to a Dynamic Polyester Platform via Sequence Selective Terpolymerisation of Elemental Sulphur.Angewandte Chemie (International ed. in English) · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
17 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Sulfur-sulfur bonds are ubiquitous across broad classes of natural products, peptides and proteins, drug molecules, and synthetic polymers and materials. The ability to make and break these bonds in a controlled manner is critical for their many scientific and technological applications. Here we report the discovery of an unusual S-S metathesis reaction of organic trisulfides. When exposed to certain polar aprotic solvents, trisulfides were found to undergo spontaneous metathesis, with the reaction equilibrium established in seconds in some cases. No exogenous reagents, heat, light or other stimuli were required to provoke this reaction. Furthermore, the trisulfide metathesis process can occur both inter- and intramolecularly. Understanding the scope and mechanism of this reaction enabled diverse applications of this chemistry in dynamic combinatorial library synthesis, the covalent modification of complex natural products, and S-S metathesis polymerization and depolymerization as a platform for chemically recyclable plastics.
Identifiers
41826675What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.