ArticleAngewandte Chemie (International ed. in English)2026
Tailoring Electronic Properties of Precision Graphene Nanoribbons via Nanopore Engineering.
Article 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.
- Iterative Synthesis of Pyrene-Coronene Molecular Graphene Nanoribbons.Angewandte Chemie (International ed. in English) · 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
20 authors.
Funding
Abstract
The precise incorporation of nanopores into graphene nanoribbons (GNRs) offers a complementary strategy for modulating their opto-electronic properties beyond conventional width and edge engineering. However, a systematic understanding of the relationship between the structure and electronic properties of porous GNRs (pGNRs) remains experimentally unexplored due to the lack of rational synthetic strategies. Herein, we report two novel porous GNRs (pGNR 1 and pGNR 2) synthesized via solution-phase methods, featuring periodically arranged [18]annulene nanopores and gulf-edged architectures, along with a nonporous GNR (npGNR) as a counterpart. Utilizing efficient Diels-Alder polymerization and Scholl-type cyclization, these GNRs attain average lengths of up to 60 nm. The chemical identities of the synthesized GNRs were comprehensively characterized by IR, Raman, and solid-state NMR spectroscopy, complemented by theoretical calculations. To further elucidate the structural features underlying the observed properties, three representative model compounds (1, 2, and 3) corresponding to segments of the respective GNRs were synthesized and analyzed. UV-vis and THz spectroscopic analyses demonstrate that npGNR exhibits a relatively narrow optical bandgap of 1.63 eV and a high intrinsic charge carrier mobility of ∼40 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.