Evidence map›Paper›PMID 41779384›Full record

ArticleAccounts of chemical research2026

Thianthrenium Salts in Photochemistry.

Zibo Bai, Tobias Ritter

Abstract read
In one paragraph

Article in Accounts of chemical research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Modern Cyanine Dye-Based Photosensitizers for Medical Applications.Angewandte Chemie (International ed. in English) · 2026
    Review
  2. 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

2 authors.

Zibo BaiMax-Planck-Institut für Kohlenforschung, D45470 Mülheim an der Ruhr, Germany.ORCID 0000-0002-0486-2519
Tobias RitterMax-Planck-Institut für Kohlenforschung, D45470 Mülheim an der Ruhr, Germany.ORCID 0000-0002-6957-450X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

ConspectusThianthrenium (TT) salts have emerged as versatile reagents with utility across transition-metal (TM) catalysis, photochemistry, biocatalysis, electrochemistry, and polar transformations. Initially introduced as an aryl (pseudo)halide surrogate in traditional TM-catalyzed cross-coupling reactions, thianthrenium salts have since demonstrated conceptually distinct advantages over their (pseudo)halide analogues in single-electron mediated processes, particularly under visible-light irradiation.The positively charged thianthrenium group raises the substrate's reduction potential into the range accessible to common photocatalysts, and upon single-electron transfer, the exocyclic C-S

Identifiers

PMID41779384
PMCPMC13001106

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.