Evidence map›Paper›PMID 38193954›Full record

ArticleJournal of fluorescence2025

Luminescent Properties of β-(hydroxyaryl)-butenolides and Fluorescence Quenching in Water.

Beatriz Miorin Finêncio, Fernanda Amorim Santos, Renato Luis Tame Parreira, Renato Pereira Orenha, Sandro Marcio Lima, Luis Humberto Cunha Andrade, Maryleide Ventura, Rosangela da Silva de Laurentiz

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Journal of fluorescence, 2025. 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
0.2field-weighted citation impact, top 67% of its field
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 citations in OpenAlex.

  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

8 authors at 4 institutions in 2 countries.

Beatriz Miorin FinêncioFaculdade de Engenharia de Ilha Solteira, Departamento de Física e Química, Universidade Estadual Paulista (Unesp), Ilha Solteira, SP, Brazil.
Fernanda Amorim SantosFaculdade de Engenharia de Ilha Solteira, Departamento de Física e Química, Universidade Estadual Paulista (Unesp), Ilha Solteira, SP, Brazil.
Renato Luis Tame ParreiraNúcleo de Pesquisas Em Ciências Exatas e Tecnológicas, Universidade de Franca, Franca, SP, Brazil.
Renato Pereira OrenhaNúcleo de Pesquisas Em Ciências Exatas e Tecnológicas, Universidade de Franca, Franca, SP, Brazil.
Sandro Marcio LimaCentro de Estudos em Recursos Naturais - CERNA, Universidade Estadual de Mato Grosso do Sul - UEMS, Dourados, MS, 79823-351, Brazil.
Luis Humberto Cunha AndradeCentro de Estudos em Recursos Naturais - CERNA, Universidade Estadual de Mato Grosso do Sul - UEMS, Dourados, MS, 79823-351, Brazil.
Maryleide VenturaCentro de Estudos em Recursos Naturais - CERNA, Universidade Estadual de Mato Grosso do Sul - UEMS, Dourados, MS, 79823-351, Brazil.
Rosangela da Silva de LaurentizFaculdade de Engenharia de Ilha Solteira, Departamento de Física e Química, Universidade Estadual Paulista (Unesp), Ilha Solteira, SP, Brazil. rosangela.laurentiz@unesp.br.
Universidade Estadual Paulista (Unesp) · BRNatura (Brazil) · BRUniversidade de Franca · BRUniversidade Estadual de Mato Grosso do Sul · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This work describes the luminescent properties of the new compound β-(hydroxyaryl)-butenolides recently discovered. The compounds were subjected to UV-Vis absorption and fluorescence analyzes when diluted in different solvents. Through the results, it was possible to observe that the β-hydroxyarylutenolides have two absorption bands, one at 289-291 nm and the other with higher intensity at 328-354 nm. The emission band between 385-422 nm is observed under excitation at 324-327 nm. The compounds showed solvatochromism as a function of the analyzed solvent. In water, fluorescence quenching of all compounds occurs. Therefore, studies with compound containing the methylenedioxy group attached in phenyl ring were carried at different concentrations of water in DMSO. The decrease in the fluorescence intensity of this compound is linearly proportional to the increase in the amount of water in the DMSO, with a minimum detection volume of 0.028%. Quantum yields of three compounds were evaluated in different solvents, showing that the relationship between the structure of the compound and the solvent is essential for a high value. The fluorescence quantum yield was also measured by Thermal Lens Spectroscopy (TLS) using DMSO as the solvent, confirming the high value for the analyzed samples. Despite being preliminary, the studies revealed that these compounds have luminescent properties that could be applied in the development of chemical sensors for detecting water in DMSO.

Indexed as

ButenolidesFluorescence quantum yieldFluorescence quenchingSolvatochromism

Identifiers

PMID38193954
OpenAlexW4390727166

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.