Evidence map›Paper›PMID 39684606›Full record

ArticleInternational journal of molecular sciences2024

Methoxyquinolone-Benzothiazole Hybrids as New Aggregation-Induced Emission Luminogens and Efficient Fluorescent Chemosensors for Cyanide Ions.

Mario Mutis-Ayala, Jorge Trilleras, Richard D'Vries, Mario A Macías, Alberto Insuasty, Rodrigo Abonia, Jairo Quiroga, Luis A Illicachi, Edgar Márquez, Daniel Insuasty

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2024. 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
–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

1 citing paper in PubMed.

  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

10 authors.

Mario Mutis-AyalaGrupo de Investigación en Compuestos Heterocíclicos, Universidad del Atlántico, Puerto Colombia 081007, Colombia.ORCID 0000-0003-4446-4774
Jorge TrillerasGrupo de Investigación en Compuestos Heterocíclicos, Universidad del Atlántico, Puerto Colombia 081007, Colombia.ORCID 0000-0002-4516-213X
Richard D'VriesGrupo de Investigación en Química de Productos Naturales, Departamento de Química, Facultad de Ciencias Naturales, Exactas y de la Educación, Universidad del Cauca, Calle 5 # 4-70, Popayán 190003, Colombia.ORCID 0000-0002-3655-1838
Mario A MacíasCristalografía y Química de Materiales, CrisQuimMat, Facultad de Ciencias, Departamento de Química, Universidad de los Andes, Cra. 1 #18a-12, Bogotá 111711, Colombia.ORCID 0000-0003-2749-8489
Alberto InsuastyGrupo de Investigación de Compuestos Heterocíclicos, Departamento de Química, Universidad del Valle, Calle 13 # 100-00, Cali 760032, Colombia.
Rodrigo AboniaGrupo de Investigación de Compuestos Heterocíclicos, Departamento de Química, Universidad del Valle, Calle 13 # 100-00, Cali 760032, Colombia.ORCID 0000-0003-3256-0961
Jairo QuirogaGrupo de Investigación de Compuestos Heterocíclicos, Departamento de Química, Universidad del Valle, Calle 13 # 100-00, Cali 760032, Colombia.ORCID 0000-0002-9451-3063
Luis A IllicachiGrupo de Investigación en Química y Biotecnología, Facultad de Ciencias Básicas, Universidad Santiago de Cali, Calle 5 # 62-00, Cali 760035, Colombia.ORCID 0000-0003-2062-9589
Edgar MárquezDepartamento de Química y Biología, División de Ciencias Básicas, Universidad del Norte, Km 5 vía Puerto Colombia, Barranquilla 081007, Colombia.ORCID 0000-0002-7503-1528
Daniel InsuastyDepartamento de Química y Biología, División de Ciencias Básicas, Universidad del Norte, Km 5 vía Puerto Colombia, Barranquilla 081007, Colombia.ORCID 0000-0001-9662-9505

Funding

Dirección General de Investigaciones of Universidad Santiago de Cali No. DGI-01-2024. 367
6 · The paper itself

Abstract

This work describes the synthesis and characterization of new quinolone-benzothiazole hybrids, the study of their aggregation-induced emission (AIE) properties, and the use of these systems as efficient fluorescent probes for cyanide ions. These conjugated derivatives are linked through a double bond favoring electronic communication, and together with their planar geometry, can strongly aggregate under solvophobic environments, leading to aggregation and exhibiting significant AIE behavior. The double bond between electroactive units is prone to nucleophilic addition reactions by cyanide ions, selectively, conducive to turning off the fluorescence properties, making this hybrid system an efficient probe for cyanide ions. These studies were theoretically explained using DFT and TD-DFT calculations.

Indexed as

BenzothiazolesCyanidesFluorescent DyesIonsMolecular StructureQuinolonesSpectrometry, FluorescencebenzothiazoleBenzothiazolesCyanidesFluorescent DyesIonsQuinolonesaggregation-induced emissionbenzothiazolechemosensorscyanidequinolone

Identifiers

PMID39684606
PMCPMC11641556

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.