Evidence map›Paper›PMID 38035251›Full record

ArticleRSC advances2023

Synthesis and evaluation of photophysical, electrochemical, and ROS generation properties of new chalcogen-naphthoquinones-1,2,3-triazole hybrids.

Luana S Gomes, Érica O Costa, Thuany G Duarte, Mateus H Köhler, Bruna M Rodrigues, Vitor F Ferreira, Fernando de C da Silva, Bernardo A Iglesias, Vanessa Nascimento

Abstract read
In one paragraph

Article in RSC advances, 2023. 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

9 authors.

Luana S GomesDepartment of Chemistry, SupraSelen Laboratory, Federal University Fluminense, Institute of Chemistry Campus do Valonguinho, Niterói 24020-141 RJ Brazil nascimentovanessa@id.uff.br.ORCID https://orcid.org/0000-0002-9159-4603
Érica O CostaDepartment of Chemistry, SupraSelen Laboratory, Federal University Fluminense, Institute of Chemistry Campus do Valonguinho, Niterói 24020-141 RJ Brazil nascimentovanessa@id.uff.br.
Thuany G DuarteDepartment of Chemistry, SupraSelen Laboratory, Federal University Fluminense, Institute of Chemistry Campus do Valonguinho, Niterói 24020-141 RJ Brazil nascimentovanessa@id.uff.br.
Mateus H KöhlerDepartment of Physics, Federal University of Santa Maria Santa Maria 97105-900 RS Brazil.ORCID https://orcid.org/0000-0001-9733-9630
Bruna M RodriguesDepartment of Chemistry, Bioinorganic and Porphyrin Materials Laboratory, Federal University of Santa Maria Santa Maria 97105-900 RS Brazil bernardopgq@gmail.com.
Vitor F FerreiraFaculty of Pharmacy, Department of Pharmaceutical Technology Niterói 24241-000 RJ Brazil.
Fernando de C da SilvaLaboratório de Síntese Orgânica Aplicada (LabSOA), Institute of Chemistry, Universidade Federal Fluminense Niterói 24020-141 RJ Brazil.ORCID https://orcid.org/0000-0002-2042-3778
Bernardo A IglesiasDepartment of Chemistry, Bioinorganic and Porphyrin Materials Laboratory, Federal University of Santa Maria Santa Maria 97105-900 RS Brazil bernardopgq@gmail.com.ORCID https://orcid.org/0000-0002-4039-6316
Vanessa NascimentoDepartment of Chemistry, SupraSelen Laboratory, Federal University Fluminense, Institute of Chemistry Campus do Valonguinho, Niterói 24020-141 RJ Brazil nascimentovanessa@id.uff.br.ORCID https://orcid.org/0000-0001-9413-7638

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study presents a comprehensive analysis encompassing the synthesis, structural elucidation, photophysical behavior, and electrochemical properties of a novel series of chalcogen-naphthoquinone-1,2,3-triazole hybrids. Employing a meticulously designed protocol, the synthesis of these hybrids, denoted as 11a-j, was achieved with remarkable efficiency (yielding up to 81%). This synthesis used a regioselective copper-catalyzed azide-alkyne cycloaddition reaction (CuAAC). Furthermore, a detailed investigation into the photophysical characteristics, TDDFT calculations, electrochemical profiles, and photobiological attributes of compounds 11a-j was conducted. This exploration aimed to unravel insights into the excited state behaviors of these molecules, as well as their redox properties. Such insights are crucial for future applications of these derivatives in diverse biological assays.

Identifiers

PMID38035251
PMCPMC10686195

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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.