ReviewAngewandte Chemie (International ed. in English)2026
Color-Pure Organic Luminophores: Characteristics, Definitions, Physical Basis and Fundamental Design Principles.
Review in Angewandte Chemie (International ed. in English), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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
1 citing paper in PubMed.
- Topological design yields MR-TADF emitters with sub-10 nm emission bandwidths.National science review · 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
7 authors.
Funding
Abstract
Color-pure all-organic emitters, i.e., with narrow spectral characteristics, are intensively studied for high-definition organic LEDs (mainly based on multi-resonance structures), as well as for multi-color bioimaging (mainly based on polymethine-like structures). To guide targeted materials design beyond tedious trial-and-error procedures, this educative review discusses the spectral characteristics (including units and unambiguous definition of the spectral width, and the occurrence of artifacts), the physical basis of the spectral broadening (vibronic coupling, environmental effects, and a basal understanding of geometries in the ground and excited states). Subsequently, the structural factors are distilled, which govern reduced geometry change between ground and excited state (GS, ES)-quantified as the change in bond-length alternation (Δ
Indexed as
Identifiers
What 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.