Evidence map›Paper›PMID 37576679›Full record

ArticleACS omega2023

Synthesis and Photophysical, Electrochemical, and DFT Studies of Piperidyl and Pyrrolidinyl Chalcones.

Humera Baig, Amber Iqbal, Alvina Rasool, Syed Zajif Hussain, Javed Iqbal, Meshari Alazmi, Nawaf Alshammari, Amira Alazmi, Amer AlGhadhban, Abdel Moneim E Sulieman and 3 more

Abstract read
In one paragraph

Article in ACS omega, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
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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

13 authors.

Humera BaigDepartment of Chemistry and Chemical Engineering, Syed Babar Ali School of Science and Engineering, Lahore University of Management Sciences, Lahore 54792, Pakistan.ORCID https://orcid.org/0000-0002-8550-9775
Amber IqbalDepartment of Chemistry and Chemical Engineering, Syed Babar Ali School of Science and Engineering, Lahore University of Management Sciences, Lahore 54792, Pakistan.
Alvina RasoolDepartment of Chemistry, University of Agriculture, Faisalabad 38000, Pakistan.
Syed Zajif HussainDepartment of Chemistry and Chemical Engineering, Syed Babar Ali School of Science and Engineering, Lahore University of Management Sciences, Lahore 54792, Pakistan.ORCID https://orcid.org/0000-0002-3834-6061
Javed IqbalDepartment of Chemistry, University of Agriculture, Faisalabad 38000, Pakistan.
Meshari AlazmiCollege of Computer Science and Engineering, University of Ha'il, P.O. Box 2440, Ha'il 81481, Saudi Arabia.
Nawaf AlshammariCollege of Sciences, University of Ha'il, P.O. Box 2440, Ha'il 81481, Saudi Arabia.
Amira AlazmiDepartment of Science and Technology, University Colleges at Nairiyah, University of Hafr Al Batin, Nairiyah, 31981, Saudi Arabia.
Amer AlGhadhbanCollege of Engineering, University of Ha'il, P.O. Box 2440, Ha'il 81481, Saudi Arabia.
Abdel Moneim E SuliemanCollege of Sciences, University of Ha'il, P.O. Box 2440, Ha'il 81481, Saudi Arabia.
Kamaleldin B SaidDepartment of Pathology and Microbiology, College of Medicine, University of Ha'il, Ha'il, 55476, Saudi Arabia.
Habib-Ur RehmanDepartment of Chemistry and Chemical Engineering, Syed Babar Ali School of Science and Engineering, Lahore University of Management Sciences, Lahore 54792, Pakistan.ORCID https://orcid.org/0000-0003-3407-5986
Rahman Shah Zaib SaleemDepartment of Chemistry and Chemical Engineering, Syed Babar Ali School of Science and Engineering, Lahore University of Management Sciences, Lahore 54792, Pakistan.ORCID https://orcid.org/0000-0002-9615-4471

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Small organic molecules with interesting optical and electrochemical properties find applications as organic luminescent materials. In this work, we report the synthesis of novel chalcones with D-A-D and D-A-D-A architecture, followed by their optical, electrochemical, and computational studies. The absorption band of these compounds occurs at 360-480 nm with emission maxima appearing around 513-552 nm. The large Stokes shifts (Δλ) for all compounds (90-132 nm) suggest intramolecular charge transfer (ICT) in the excited states. The molar absorptivity and fluorescence quantum yields were found to be in the range of 1.7-4.26 × 10

Identifiers

PMID37576679
PMCPMC10413825

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LicenceCC BY-NC-ND
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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.