Evidence map›Paper›PMID 42289780›Full record

ArticleChemistry, an Asian journal2026

Synthesis, Characterization, and Photobiological Evaluation of Novel Acetyl-Glycosylated Corroles as Potential Photosensitizers.

Carlos C Diniz, Thiago B de Souza, Ricardo J Alves, Eduarda Duarte, Helena C Junqueira, Divinomar Severino, Angela P Y Candela, Diego F de Oliveira, Leonardo De Boni, Vinícius N da Rocha and 3 more

Abstract read
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In one paragraph

Article in Chemistry, an Asian journal, 2026. 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

13 authors.

Carlos C DinizBioinorganic and Porphyrinoid Material Laboratory, Department of Chemistry, Federal University of Santa Maria, Santa Maria, Rio Grande do Sul, Brazil.
Thiago B de SouzaSchool of Pharmacy, Federal University of Ouro Preto, Ouro Preto, Minas Gerais, Brazil.
Ricardo J AlvesFaculty of Pharmacy, Federal University of Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.
Eduarda DuarteInstitute of Chemistry, São Paulo University, São Paulo, São Paulo, Brazil.
Helena C JunqueiraInstitute of Chemistry, São Paulo University, São Paulo, São Paulo, Brazil.
Divinomar SeverinoInstitute of Chemistry, São Paulo University, São Paulo, São Paulo, Brazil.
Angela P Y CandelaInstitute of Chemistry, São Paulo University, São Paulo, São Paulo, Brazil.
Diego F de OliveiraSão Carlos Institute of Physics, São Paulo University, São Carlos, São Paulo, Brazil.
Leonardo De BoniSão Carlos Institute of Physics, São Paulo University, São Carlos, São Paulo, Brazil.ORCID https://orcid.org/0000-0002-1875-1852
Vinícius N da RochaDepartment of Physics, Federal University of Santa Maria, Santa Maria, Rio Grande do Sul, Brazil.
Paulo C PiquiniDepartment of Physics, Federal University of Santa Maria, Santa Maria, Rio Grande do Sul, Brazil.ORCID https://orcid.org/0000-0003-4340-2723
Mauricio S BaptistaInstitute of Chemistry, São Paulo University, São Paulo, São Paulo, Brazil.ORCID https://orcid.org/0000-0001-7079-7666
Bernardo A IglesiasBioinorganic and Porphyrinoid Material Laboratory, Department of Chemistry, Federal University of Santa Maria, Santa Maria, Rio Grande do Sul, Brazil.ORCID https://orcid.org/0000-0002-4039-6316

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 303287/2024-1Coordenação de Aperfeiçoamento de Pessoal de Nível Superior Finance Code 001Fundação de Amparo à Pesquisa do Estado de São Paulo 2021/07350-3Fundação de Amparo à Pesquisa do Estado de São Paulo 2023/05917-1Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul 21/2551-0002114-4Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul 24/2551-0001939-1São Paulo Research Foundation
6 · The paper itself

Abstract

This work reports the synthesis, structural characterization, and photophysical and electrochemical evaluation of a novel series of mono-(acetyl-glycosylated) free-base corroles. The molecules were prepared using classical Gryko methodologies, yielding four new acetyl-glycosylated derivatives alongside a nonglycosylated reference compound. A complete spectroscopic and analytical characterization was performed, including absorption, steady-state, and time-resolved fluorescence, and electrochemical studies. Detailed analysis of the singlet and triplet excited states, supported by DFT calculations and natural transition orbital (NTO) analysis, confirmed the nature of the electronic transitions and provided insight into excited-state geometries. Furthermore, the derivatives were evaluated for key photobiological properties: all compounds demonstrated efficient singlet oxygen (

Indexed as

acetyl‐glycosilated corrolescorrolesphotobiologyphotophysics

Identifiers

PMID42289780
PMCPMC13355094

What OpenQuestion holds

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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.