ArticleChemistry (Weinheim an der Bergstrasse, Germany)2025
Fluorescent Carbazole-Derived Aza[5]Helicenes: Synthesis, Functionalization, and Characterization.
Article in Chemistry (Weinheim an der Bergstrasse, Germany), 2025. 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
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
2 citing papers in PubMed.
- Aza[6]- and Aza[7]helicenes: Synthesis and Reversible Protonation-Induced Tuning of Photophysical and Chiroptical Properties.JACS Au · 2026Article
- Synthesis and Characterization of Carbazole-Containing Aza[7]helicenes.Chemistry (Weinheim an der Bergstrasse, Germany) · 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
3 authors.
Funding
Abstract
5,8-Dihydroindolo[2,3-c]carbazole (ICz), 9H-cinnolino[3,4-c]carbazole (CnCz), and variously alkyl-, alkenyl-, and aryl-substituted indolo[2,3-k]- and -[3,2-a]phenanthridines (IPs) were synthesized using an ortho fusion strategy with Suzuki cross couplings, intramolecular nitrene insertions, diazo couplings, and Morgan-Walls cyclizations as key reactions. The IPs were additionally transformed into organoboranes and helicene conjugates with tetraphenylethylene derivatives. The compounds fluoresce with large Stokes shifts, exhibit strong acidochromism, and show a good to excellent aggregation-induced emission. Their helical structure was elucidated by x-ray crystallographic analysis and by quantum chemical calculations. HOMO-LUMO gaps of 3.96-4.06 eV and S
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.