ArticleNature communications2024
A Janus carbaporphyrin pseudo-dimer.
Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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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.
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Who cites it
4 citing papers in PubMed.
- Bis(10-oxacorrole) with Fused Pyridine as a Linker: Synthesis, Structure, and Interaction between the Subunits in the Neutral, Mono-, and Dicationic States.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025Article
- Pyridine-Fused Bis(azacorrole)s: Easily Accessible NIR III Absorbing Cation Radicals and Biradicaloids of Antiaromatic Ground State.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
- Ruthenocenoporphyrinoids─π-Conjugation Transmitted across 1,3-Substituted Ruthenocene.Inorganic chemistry · 2025Article
- Precisely metal doped nanographenes via a carbaporphyrin approach.Nature communications · 2025Article
Corrections and comments
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Authors and funding
9 authors.
Funding
Abstract
Carbaporphyrin dimers, investigated for their distinctive electronic structures and exceptional properties, have predominantly consisted of systems containing identical subunits. This study addresses the associated knowledge gap by focusing on asymmetric carbaporphyrin dimers with Janus-like characteristics. The synthesis of a Janus-type carbaporphyrin pseudo-dimer 5 is presented. It displays antiaromatic characteristics on the fused side and nonaromatic behavior on the unfused side. A newly synthesized tetraphenylene (TPE) linked bis-dibenzihomoporphyrin 8 and a previously reported dibenzo[g,p]chrysene (DBC) linked bis-dicarbacorrole 9 were prepared as controls. Comprehensive analyses, including
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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.