Evidence map›Paper›PMID 40206553›Full record

ArticleChemical science2025

Water-soluble BODIPY dyes: a novel approach for their sustainable chemistry and applied photonics.

Christopher Schad, Cesar Ray, Carolina Díaz-Norambuena, Sergio Serrano-Buitrago, Florencio Moreno, Beatriz L Maroto, Inmaculada García-Moreno, Mónica Muñoz-Úbeda, Iván López-Montero, Jorge Bañuelos and 1 more

Abstract read
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Article in Chemical science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

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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

11 authors.

Christopher SchadDepartamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n Madrid 28040 Spain santmoya@ucm.es.
Cesar RayDepartamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n Madrid 28040 Spain santmoya@ucm.es.
Carolina Díaz-NorambuenaDepartamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n Madrid 28040 Spain santmoya@ucm.es.
Sergio Serrano-BuitragoDepartamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n Madrid 28040 Spain santmoya@ucm.es.
Florencio MorenoDepartamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n Madrid 28040 Spain santmoya@ucm.es.ORCID https://orcid.org/0000-0002-7966-5157
Beatriz L MarotoDepartamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n Madrid 28040 Spain santmoya@ucm.es.ORCID https://orcid.org/0000-0003-0299-1197
Inmaculada García-MorenoDepartamento de Química-Física de Materiales, Instituto de Química-Física Blas Cabrera, Consejo Superior de Investigaciones Científicas (CSIC) Serrano 119 Madrid 28006 Spain.
Mónica Muñoz-ÚbedaDepartamento de Química Física, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n 28040 Madrid Spain.
Iván López-MonteroDepartamento de Química Física, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n 28040 Madrid Spain.ORCID https://orcid.org/0000-0001-8131-6063
Jorge BañuelosDepartamento de Química-Física, Facultad de Ciencia y Tecnología, Universidad del País Vasco-EHU Bilbao 48080 Spain jorge.banuelos@ehu.eus.ORCID https://orcid.org/0000-0002-8444-4383
Santiago de la MoyaDepartamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria s/n Madrid 28040 Spain santmoya@ucm.es.ORCID https://orcid.org/0000-0002-7406-909X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The BODIPY family of organic dyes has emerged as a cornerstone in photonics research development, driving innovation and advancement in various fields of high socio-economic interest. However, the majority of BODIPY dyes exhibit hydrophobic characteristics, resulting in poor solubility in water and other hydrophilic solvents. This solubility is paramount for their optimal utilization in a myriad of photonic applications, particularly in the realms of biology and medicine. Furthermore, it facilitates safer and more sustainable manipulation and chemical modification of these expansive dyes. Nevertheless, bestowing BODIPYs with water solubility while preserving their other essential properties, notably their photophysical signatures, poses a significant challenge. In this context, we present a straightforward general chemical modification aimed at converting conventional hydrophobic BODIPYs into highly hydrophilic variants, thus enabling their efficient solubilization in water and other hydrophilic solvents with minimal disruption to the dye's inherent photophysics. The efficacy of this methodology is demonstrated through the synthesis of a number of water-soluble BODIPY dyes featuring diverse substitution patterns. Furthermore, we showcase their utility in a spectrum of photonics-related applications, including in-water BODIPY chemistry and dye-laser technology, and fluorescence microscopy.

Identifiers

PMID40206553
PMCPMC11976447

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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.