ArticleJACS Au2026
Long-Lived Terphenyl Radical Anion Super-Reductant for Photocatalysis Formed via Blue-to-UV Upconversion with Fully Resolved Mechanism.
Article in JACS Au, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
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.
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
3 citing papers in PubMed.
- Evidence of static quenching in the photoredox activity of perylene diimide radical anions: implications for consecutive photoinduced electron transfer photocatalysis.Chemical science · 2026Article
- A Metal-Organic Framework Platform Enabling Visible-to-Ultraviolet Upconversion-Driven Heterogeneous Photochemistry.JACS Au · 2026Article
- Mechanistic Design in Photocatalysis.Accounts of chemical research · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Biphotonic mechanisms with visible light excitation can generate highly reactive species for thermodynamically challenging reactions. Particularly prominent is the consecutive photoinduced electron transfer mechanism, in which excited radical ions are the presumed key catalytically active species. They benefit from extremely high redox powers but suffer from excited state lifetimes in the low picosecond range and are susceptible to photodegradation. This makes mechanistic elucidation difficult and sometimes leads to debate around the identity of the true catalytically active species. In this study, we address these challenges by presenting a fully resolved mechanism, in which a spectroscopically observable and quantifiable ground state
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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 Socratic graph.