Evidence map›Paper›PMID 40944394›Full record

ArticleAngewandte Chemie (International ed. in English)2025

Spatiotemporal Control of the Formation of Luminescent Lanthanide Complexes in Liposome-Based Nanoreactors.

Aaron Torres-Huerta, Miriam de J Velásquez-Hernández, Elena Tamarit-Amoros, Marina Raschetti, Daniel Pinkas, Ondřej Jurček, Javier Pérez, Hennie Valkenier

Abstract read
In one paragraph

Article in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Color-tunable luminescent TbCell reports. Physical science · 2026
    Article
  2. Article
  3. 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.

Aaron Torres-HuertaEngineering of Molecular NanoSystems (EMNS), Université libre de Bruxelles, Avenue F. Roosevelt 50, CP165/64, Brussels, B-1050, Belgium.ORCID 0000-0002-3251-1855
Miriam de J Velásquez-HernándezCenter for Membrane Separations, Adsorption, Catalysis, and Spectroscopy (cMACS), KU Leuven, Leuven, 3001, Belgium.ORCID 0000-0002-1338-4459
Elena Tamarit-AmorosEngineering of Molecular NanoSystems (EMNS), Université libre de Bruxelles, Avenue F. Roosevelt 50, CP165/64, Brussels, B-1050, Belgium.
Marina RaschettiCNRS, Institut FEMTO-ST, Université Marie et Louis Pasteur, Besançon, F-25000, France.
Daniel PinkasCEITEC - Central European Institute of Technology, Masaryk University, Kamenice 5, Brno, CZ-62500, Czechia.ORCID 0000-0002-4365-4181
Ondřej JurčekDepartment of Natural Drugs, Faculty of Pharmacy, Masaryk University, Palackého 1946/1, Brno, CZ-61200, Czechia.ORCID 0000-0002-9809-656X
Javier PérezSynchrotron SOLEIL, Gif-sur-Yvette, F-91192, France.ORCID 0000-0003-3083-4754
Hennie ValkenierEngineering of Molecular NanoSystems (EMNS), Université libre de Bruxelles, Avenue F. Roosevelt 50, CP165/64, Brussels, B-1050, Belgium.ORCID 0000-0002-4409-0154

Funding

European Research Council 802727European Union's Horizon 2020 research and innovation programme 101007417European Union's Horizon Europe research and innovation programme 101065037Fonds de la Recherche Scientifique - FNRSInnovation of Czech Infrastructure for Integrative Structural Biology CZ.02.01.01/00/23_015/0008175Ministerstvo školství, mládeže a tělovýchovy (in English: Ministry of Education Youth and Sports, MEYS) LM2023042
6 · The paper itself

Abstract

The controlled mass transfer across compartmentalised environments in synthetic nanoreactors is essential for enhancing precise spatiotemporal manipulation of chemical transformations within confined spaces. In this study, we present a strategy that integrates a synthetic anion transporter in liposome-based nanoreactors, allowing for spatiotemporal control over the formation of metal-organic complexes in liposomes. This approach enables us to effectively modulate the assembly of luminescent lanthanide-benzenedicarboxylate nanostructures. Fluorescence studies demonstrate that the reaction rate can be customised by varying the anion transporter concentration, which dictates the rate of entry of the carboxylate ligand. Changes in the morphology of the liposome nanoreactors due to the assisted transmembrane transport of benzenedicarboxylate were investigated using cryo-TEM and time-resolved SAXS measurements, which revealed a structural transformation of the lipid bilayer during the complex formation. Our findings provide a novel platform for exploring coordination chemistry in nanoscale confinements, opening avenues for the design of biohybrid materials.

Indexed as

Coordination ComplexesLanthanoid Series ElementsLiposomesNanostructuresLuminescenceCoordination ComplexesLanthanoid Series ElementsLiposomesIon transportLanthanide complexesLiposomesNanoreactorsNanostructures

Identifiers

PMID40944394
PMCPMC12582006

What OpenQuestion holds

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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.