ArticleAngewandte Chemie (International ed. in English)2025
Azuperylene: The Nonalternant Isomer of Perylene.
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 6 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
6 citing papers in PubMed.
- Azulene-Fused Polycyclic Aromatic Hydrocarbons: Synthesis, Structural, Optical, and Electrochemical Properties of Azuleno[1,2,3-cd]Benzo[mn]Pyrene-8,14-diones and Cyclohepta[1,2]Indeno[6,5,4-de]Anthracen-9-ones.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026Article
- Bottom-Up Approach for the Synthesis of Contorted Nanographenes by Cp*Co(III)-Catalyzed Annulative-π-Extension-Cyclization Cascade.Chemistry (Weinheim an der Bergstrasse, Germany) · 2026Article
- π-Electron reorganization in polycyclic aromatic hydrocarbons toward BT.2020-compliant narrowband red emitters.National science review · 2026Article
- A CJournal of the American Chemical Society · 2026Article
- Azuperylene: The Nonalternant Isomer of Perylene.Angewandte Chemie (International ed. in English) · 2025Article
- Recent advances and future challenges in the bottom-up synthesis of azulene-embedded nanographenes.Beilstein journal of organic chemistry · 2025Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
11 authors.
Funding
Abstract
The isoelectronic isomer of perylene, hereafter called as azuperylene, has been prepared. Electronic structure analysis reveals that the new isomer can be described as a union of two antiparallel azulenes in which the azulene-type aromatic character of the starting azulene is partially retained. Four 2,8-dialkoxy (i.e., ethoxy, n-butoxy, n-hexyloxy, and n-octyloxy) functionalized derivatives of the new isomer core have been prepared. The solid-state structures of the new compounds have been resolved showing exceptional herringbone π-π stacking ideal for charge transport. Organic field-effect transistors on sublimated substrates display an excellent hole transport mobility up to 1.03 cm
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.