Evidence map›Paper›PMID 40575836›Full record

ArticleChemistry, an Asian journal2025

Synthesis, Structures, and Properties of Dehydrobiphenyleno[12]Annulenes: Carbon-Rich Compounds Comprising Two Different Antiaromatic Units.

Komari Suzuki, Daisuke Asai, Robert J Herman, Sheila W Njoroge, Satoshi Yoshida, Sota Sato, Semin Lee, Kazukuni Tahara

Abstract read
In one paragraph

Article in Chemistry, an Asian journal, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Komari SuzukiDepartment of Applied Chemistry, School of Science and Technology, Meiji University, 1-1-1 Higashimita, Tama-ku, Kawasaki, Kanagawa, 214-8571, Japan.
Daisuke AsaiDepartment of Applied Chemistry, School of Science and Technology, Meiji University, 1-1-1 Higashimita, Tama-ku, Kawasaki, Kanagawa, 214-8571, Japan.
Robert J HermanDepartment of Chemistry, Louisiana State University, Baton Rouge, Louisiana, 70803, USA.ORCID https://orcid.org/0000-0003-4812-6246
Sheila W NjorogeDepartment of Chemistry, Louisiana State University, Baton Rouge, Louisiana, 70803, USA.ORCID https://orcid.org/0009-0007-9723-8849
Satoshi YoshidaDepartment of Applied Chemistry, School of Engineering, The University of Tokyo, Mitsui Link Lab Kashiwanoha 1, FS CREATION, 6-6-2 Kashiwanoha, Kashiwa, Chiba, 277-0882, Japan.
Sota SatoDepartment of Applied Chemistry, School of Engineering, The University of Tokyo, Mitsui Link Lab Kashiwanoha 1, FS CREATION, 6-6-2 Kashiwanoha, Kashiwa, Chiba, 277-0882, Japan.
Semin LeeDepartment of Chemistry, Louisiana State University, Baton Rouge, Louisiana, 70803, USA.ORCID https://orcid.org/0000-0003-0873-9507
Kazukuni TaharaDepartment of Applied Chemistry, School of Science and Technology, Meiji University, 1-1-1 Higashimita, Tama-ku, Kawasaki, Kanagawa, 214-8571, Japan.

Funding

Iketani Science and Technology FoundationInstitute of Science and TechnologyMeiji University, Tokuyama Science FoundationNational Science Foundation NSF CHE 1956302
6 · The paper itself

Abstract

In this work we report the synthesis, structure, and electronic properties of carbon-rich compounds dehydrobiphenyleno[12]annulenes (DBP[12]As) comprising antiaromatic four-membered rings (4MR) and 12-membered ring (12MR). Ultraviolet-visible absorption spectra and electrochemical behaviors of DBP[12]As confirmed their relatively narrow highest occupied molecular orbital (HOMO)-lowest unoccupied molecular orbital (LUMO) gap values and high HOMO energy levels, which were supported by density functional theory simulations. Parent DBP[12]A adopts a slipped herringbone structure in a crystalline state, with the molecules forming 1D stacks via π-π interactions. The experimentally derived bond lengths, bonding analyses using the Wiberg bond indices, and localized orbital locator calculation support a stronger double bond character for the 12MR bonds than the 4MR bonds in the inner six-membered ring. The chemical shifts of hydrogens in

Indexed as

AntiaromaticityBiphenyleneCarbon rich compoundsDehydro[12]annuleneElectronic properties

Identifiers

PMID40575836
PMCPMC12450042

What OpenQuestion holds

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Registered trials

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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.