Evidence map›Paper›PMID 41634251›Full record

ArticleScientific reports2026

Schleyer-type hyperconjugative aromaticity in CH isomers of diazoles revealed by DFT and NBO analysis.

Pardis Naderi Dehkordi, Hamid Saeidian, Zohreh Mirjafary, Morteza Rouhani

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

4 authors.

Pardis Naderi DehkordiDepartment of Chemistry, SR.C, Islamic Azad University, Tehran, Iran.
Hamid SaeidianDepartment of Science, Payame Noor University (PNU), PO Box: 19395 - 4697, Tehran, Iran. saeidian1980@pnu.ac.ir.
Zohreh MirjafaryDepartment of Chemistry, SR.C, Islamic Azad University, Tehran, Iran.
Morteza RouhaniDepartment of Chemistry, SR.C, Islamic Azad University, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aromaticity is a central concept in organic chemistry, traditionally evaluated through structural, magnetic, and electronic criteria. In this study, density functional theory (DFT) calculations were performed to systematically investigate the impact of various substituents (-H, -Me, -CH₂-CH₂-, -F, -Cl, -SiH₃, -GeH

Indexed as

AromaticityCH tautomer of diazole derivativesDFTHOMEDHyperconjugationNBONICSSchleyer-type aromaticity

Identifiers

PMID41634251
PMCPMC12921015

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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.