ReviewRSC advances2021
Scholl reaction as a powerful tool for the synthesis of nanographenes: a systematic review.
Review in RSC advances, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 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
16 citing papers in PubMed, 86 citations in OpenAlex.
- Diversity-Oriented Two-Step Annulative π-Extension Enables Access to Structurally Complex Nanographenes.Angewandte Chemie (International ed. in English) · 2026Article
- π-Radical Cascades to Peri-Fused Triangulene Dimers.Angewandte Chemie (International ed. in English) · 2026Article
- 1,4-Diazatriphenylene and Its Hetero-Fused Analogs: Synthesis and Applications.Molecules (Basel, Switzerland) · 2026Review
- Triphenylene as a versatile scaffold for advanced functional materials.RSC advances · 2026Review
- Indeno[2,1-c]fluorene Quasi[8]circulenes Through Intramolecular Cyclization.Angewandte Chemie (International ed. in English) · 2025Article
- Twenty Years of Graphene: From Pristine to Chemically Engineered Nano-Sized Flakes.Journal of the American Chemical Society · 2024Review
- Phenylsulfonate as a photolabile group for intramolecular carbon-carbon cross-coupling reactions.RSC advances · 2024Article
- Theoretical Study on Vibrationally Resolved Electronic Spectra of Chiral Nanographenes.Molecules (Basel, Switzerland) · 2024Article
- A π-extended β-diketiminate ligandChemical communications (Cambridge, England) · 2024Article
- Copper-catalysed perarylation of cyclopentadiene: synthesis of hexaarylcyclopentadienes.Chemical science · 2024Article
- Synthesis and Structural and Optical Behavior of Dehydrohelicene-Containing Polycyclic Compounds.Molecules (Basel, Switzerland) · 2024Review
- Understanding the Optical Properties of Doped and Undoped 9-Armchair Graphene Nanoribbons in Dispersion.ACS nano · 2023Article
- Helical Bilayer Nanographenes: Impact of the Helicene Length on the Structural, Electrochemical, Photophysical, and Chiroptical Properties.Journal of the American Chemical Society · 2023Article
- Electronic Control of the Scholl Reaction: Selective Synthesis of Spiro vs Helical Nanographenes.Angewandte Chemie (International ed. in English) · 2023Article
- Exploring the Acid-Catalyzed Reactions of 10,11-Epoxy-Dibenzo[ACS omega · 2022Article
- Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors at 5 institutions in 4 countries.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Nanographenes, or extended polycyclic aromatic hydrocarbons, have been attracting increasing attention owing to their widespread applications in organic electronics. However, the atomically precise fabrication of nanographenes has thus far been achieved only through synthetic organic chemistry. Polycyclic aromatic hydrocarbons (PAHs) are popular research subjects due to their high stability, rigid planar structure, and characteristic optical spectra. The recent discovery of graphene, which can be regarded as giant PAH, has further stimulated research interest in this area. Chemists working with nanographene and heterocyclic analogs thereof have chosen it as their preferred tool for the assembly of large and complex architectures. The Scholl reaction has maintained significant relevance in contemporary organic synthesis with many advances in recent years and now ranks among the most useful C-C bond-forming processes for the generation of the π-conjugated frameworks of nanographene or their heterocyclic analogs. A broad range of oxidants and Lewis acids have found use in Scholl-type processes, including Cu(OTf)
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.