Evidence map›Paper›PMID 40765305›Full record

ArticleAngewandte Chemie (International ed. in English)2025

Copper Single-Atom Catalyst for Efficient C─S Coupling in Thioether Synthesis.

Theodore A Gazis, Shilpa Palit, Luis A Cipriano, Nicolò Allasia, Sean M Collins, Quentin M Ramasse, Ik Seon Kwon, Martin Sterrer, Giovanni Di Liberto, Gianvito Vilé

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Copper Single-Atom Catalyst for Efficient C─S Coupling in Thioether Synthesis.Angewandte Chemie (International ed. in English) · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Theodore A Gazis *Department of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di Milano, Piazza Leonardo da Vinci 32, Milano, 20133, Italy.
Shilpa Palit *Department of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di Milano, Piazza Leonardo da Vinci 32, Milano, 20133, Italy.
Luis A CiprianoDepartment of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di Milano, Piazza Leonardo da Vinci 32, Milano, 20133, Italy.
Nicolò AllasiaDepartment of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di Milano, Piazza Leonardo da Vinci 32, Milano, 20133, Italy.
Sean M CollinsBragg Centre for Materials Research, School of Chemical and Process Engineering & School of Chemistry, University of Leeds, Woodhouse Lane, Leeds, LS2 9JT, UK.
Quentin M RamasseSuperSTEM Laboratory, SciTech Daresbury Campus, Keckwick Lane, Daresbury, WA4 4AD, UK.
Ik Seon KwonDepartment of Energy Science and Engineering, Kunsan National University, 558 Daehak-ro, Gunsan-si, Republic of Korea.
Martin SterrerInstitute of Physics, University of Graz, Universitätsplatz 5, Graz, 8010, Austria.
Giovanni Di LibertoDepartment of Materials Science, University of Milan Bicocca, via Roberto Cozzi 55, Milano, 20125, Italy.
Gianvito ViléDepartment of Chemistry, Materials, and Chemical Engineering "Giulio Natta", Politecnico di Milano, Piazza Leonardo da Vinci 32, Milano, 20133, Italy.ORCID https://orcid.org/0000-0003-0641-8590

Funding

Engineering and Physical Sciences Research Council EP/W021080/1Engineering and Physical Sciences Research Council EP/X035123/1European Commission through a Marie Skłodowska-Curie Fellowship 101152890European Research Council 101075832 SAC_2.0European Union's Horizon Europe programme "Global Challenges and European Industrial Competitiveness" for the "SusPharma" project 101057430European Union under the National Recovery and Resilience Plan (PNRR)Italian "Dottorato Nazionale in Catalisi"Italian Ministry of University and Research (MUR)
6 · The paper itself

Abstract

Carbon-heteroatom cross-coupling reactions have become indispensable tools in synthetic chemistry. However, the formation of carbon-sulfur (C─S) bonds, which are essential for producing thioethers used in pharmaceuticals, agrochemicals, and advanced materials, remains significantly underdeveloped. Industrial C─S coupling methods still rely on expensive, homogeneous catalysts that suffer from poor recyclability and are susceptible to sulfur-induced deactivation. In this work, we report a copper single-atom catalyst, where Cu sites are atomically dispersed on mesoporous graphitic carbon nitride, to enable efficient, selective, and recyclable C─S cross-coupling reactions under mild conditions and on a gram scale. The catalyst exhibits excellent resistance to thiol poisoning and maintains high performance over multiple catalytic cycles. Advanced characterization techniques, including aberration-corrected electron microscopy, X-ray absorption spectroscopy, and single-atom-sensitive electron energy loss spectroscopy, confirm the atomic dispersion and stable coordination environment of Cu sites. Combined with density functional theory simulations and radical scavenging experiments, our mechanistic investigations support a concerted oxidative addition pathway, which excludes radical intermediates. These results provide key insights into heterogeneous C─S coupling and demonstrate the power of single-atom catalysts in addressing long-standing challenges in sulfur chemistry, paving the way toward greener and more scalable processes for fine chemical and pharmaceutical synthesis.

Indexed as

Cross‐coupling reactionsC─S Bond formationDensity functional theoryFine chemical synthesisSingle‐atom catalysis

Identifiers

PMID40765305
PMCPMC12435431

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Registered trials

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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.