Evidence map›Paper›PMID 40521459›Full record

ArticleACS omega2025

Radical Formation by Direct Single Electron Transfer between Nitrobenzene and Anionic Organo Bases.

Shivaprasad Achary Balahoju, Nicholus Bhattacharjee, Luis Lezama, Xabier Lopez, Pablo Salcedo-Abraira, Antonio Rodríguez-Diéguez, Daniel Reta

Abstract read
In one paragraph

Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Shivaprasad Achary BalahojuDonostia International Physics Centre (DIPC), Paseo Manuel Lardizabal 4, Donostia 20018, Euskadi, Spain.
Nicholus BhattacharjeeDonostia International Physics Centre (DIPC), Paseo Manuel Lardizabal 4, Donostia 20018, Euskadi, Spain.
Luis LezamaInorganic Chemistry, University of the Basque Country, Barrio Sarriena, s/n, 48940 Leioa, Bizkaia, Spain.ORCID https://orcid.org/0000-0001-6183-2052
Xabier LopezDepartment of Polymers and Advanced Materials, Faculty of Chemistry, The University of the Basque Country, UPV/EHU, Paseo Manuel Lardizabal 3, Donostia 20018, Euskadi, Spain.ORCID https://orcid.org/0000-0002-2711-3588
Pablo Salcedo-AbrairaDepartment of Inorganic Chemistry, University of Granada. Av. Fuente Nueva s/n, 18071 Granada, Spain.ORCID https://orcid.org/0000-0003-4812-8938
Antonio Rodríguez-DiéguezDepartment of Inorganic Chemistry, University of Granada. Av. Fuente Nueva s/n, 18071 Granada, Spain.ORCID https://orcid.org/0000-0003-3198-5378
Daniel RetaDonostia International Physics Centre (DIPC), Paseo Manuel Lardizabal 4, Donostia 20018, Euskadi, Spain.ORCID https://orcid.org/0000-0003-0000-9892

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The presence of unpaired electrons, i.e., radicals, equips organic molecules with unique magnetic and reactivity properties. However, due to the reactive nature of radicals and the nontrivial chemistry required for their preparation, strict structural and electronic limitations are imposed on the available systems, limiting their potential applications. Thus, developing mechanisms that enable facile radical formation in simple reaction conditions, employing available and inexpensive reactants and applicable to general types of molecules, holds the key to capitalize on the extraordinary properties that radicals have to offer. Here, combining electron paramagnetic resonance spectroscopy and ab initio calculations, we uncover an unprecedented single electron transfer from multiple anionic organic bases (B

Identifiers

PMID40521459
PMCPMC12163852

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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.