Evidence map›Paper›PMID 41965387›Full record

ArticleScientific reports2026

Photophysical investigation of green vitamin C adducts as synthetic pH indicators: solvatochromism, halochromism, and DFT calculations integrating optical band gap and electronic transition analysis.

Srood Omer Rashid

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Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

1 author.

Srood Omer RashidDepartment of Chemistry, College of Science, University of Sulaimani, Qlyasan Street, Sulaymaniyah, 46001, Iraq. srood.rashid@univsul.edu.iq.ORCID http://orcid.org/0000-0002-0179-2981

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The chemistry of vitamin C adducts was revisited to investigate their pH sensitivity, photophysical properties, optical behavior, and assess their potential as eco-friendly pH indicators. In this study, a series of ascorbic acid adducts were synthesized through a straightforward, high-yield method. Their acid-base responsiveness is driven by a reversible protonation-deprotonation process between the hydrazineyl and azo groups, causing observable color changes. Analysis of substituent effects demonstrated that strong electron-withdrawing groups like nitro (-NO₂) significantly impact the electronic structure, particularly when located at the ortho or para positions of the aromatic ring. Solvatochromic studies revealed that the ortho-nitro adduct 3(b) and para-nitro adduct 3(d) exhibited positive solvatochromism, with their absorption wavelengths increasing in more polar solvents. Notably, 3(b) displayed a consistent yellow color with λ

Indexed as

Acid–base indicatorsAscorbic acidBand gapComputational chemistryOptical propertiespH sensorSynthetic dyes

Identifiers

PMID41965387

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.