Evidence map›Paper›PMID 35458640›Full record

ReviewMolecules (Basel, Switzerland)2022

Excited-State Intramolecular Proton Transfer Dyes with Dual-State Emission Properties: Concept, Examples and Applications.

Timothée Stoerkler, Thibault Pariat, Adèle D Laurent, Denis Jacquemin, Gilles Ulrich, Julien Massue

Abstract readReview
In one paragraph

Review in Molecules (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Article
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  15. ESIPT-Capable 4-(2-Hydroxyphenyl)-2-(Pyridin-2-yl)-1Molecules (Basel, Switzerland) · 2023
    Article
  16. Review
  17. 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

6 authors.

Timothée StoerklerInstitut de Chimie et Procédés pour l'Energie, l'Environnement et la Santé (ICPEES), Equipe Chimie Organique pour la Biologie, les Matériaux et l'Optique (COMBO), UMR CNRS 7515, Ecole Européenne de Chimie, Polymères et Matériaux (ECPM), Université de Strasbourg, 25 Rue Becquerel, CEDEX 02, 67087 Strasbourg, France.
Thibault PariatInstitut de Chimie et Procédés pour l'Energie, l'Environnement et la Santé (ICPEES), Equipe Chimie Organique pour la Biologie, les Matériaux et l'Optique (COMBO), UMR CNRS 7515, Ecole Européenne de Chimie, Polymères et Matériaux (ECPM), Université de Strasbourg, 25 Rue Becquerel, CEDEX 02, 67087 Strasbourg, France.
Adèle D LaurentChimie et Interdisciplinarités: Synthèse, Analyse et Modélisation (CEISAM), UMR CNRS 6230, Nantes University, 44322 Nantes, France.ORCID 0000-0001-9553-9014
Denis JacqueminChimie et Interdisciplinarités: Synthèse, Analyse et Modélisation (CEISAM), UMR CNRS 6230, Nantes University, 44322 Nantes, France.
Gilles UlrichInstitut de Chimie et Procédés pour l'Energie, l'Environnement et la Santé (ICPEES), Equipe Chimie Organique pour la Biologie, les Matériaux et l'Optique (COMBO), UMR CNRS 7515, Ecole Européenne de Chimie, Polymères et Matériaux (ECPM), Université de Strasbourg, 25 Rue Becquerel, CEDEX 02, 67087 Strasbourg, France.
Julien MassueInstitut de Chimie et Procédés pour l'Energie, l'Environnement et la Santé (ICPEES), Equipe Chimie Organique pour la Biologie, les Matériaux et l'Optique (COMBO), UMR CNRS 7515, Ecole Européenne de Chimie, Polymères et Matériaux (ECPM), Université de Strasbourg, 25 Rue Becquerel, CEDEX 02, 67087 Strasbourg, France.ORCID 0000-0002-0629-4949

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dual-state emissive (DSE) fluorophores are organic dyes displaying fluorescence emission both in dilute and concentrated solution and in the solid-state, as amorphous, single crystal, polycrystalline samples or thin films. This comes in contrast to the vast majority of organic fluorescent dyes which typically show intense fluorescence in solution but are quenched in concentrated media and in the solid-state owing to π-stacking interactions; a well-known phenomenon called aggregation-caused quenching (ACQ). On the contrary, molecular rotors with a significant number of free rotations have been engineered to show quenched emission in solution but strong fluorescence in the aggregated-state thanks to restriction of the intramolecular motions. This is the concept of aggregation-induced emission (AIE). DSE fluorophores have been far less explored despite the fact that they are at the crossroad of ACQ and AIE phenomena and allow targeting applications both in solution (bio-conjugation, sensing, imaging) and solid-state (organic electronics, data encryption, lasing, luminescent displays). Excited-State Intramolecular Proton Transfer (ESIPT) fluorescence is particularly suitable to engineer DSE dyes. Indeed, ESIPT fluorescence, which relies on a phototautomerism between normal and tautomeric species, is characterized by a strong emission in the solid-state along with a large Stokes' shift, an enhanced photostability and a strong sensitivity to the close environment, a feature prone to be used in bio-sensing. A drawback that needs to be overcome is their weak emission intensity in solution, owing to detrimental molecular motions in the excited-state. Several strategies have been proposed in that regard. In the past few years, a growing number of examples of DSE-ESIPT dyes have indeed emerged in the literature, enriching the database of such attractive dyes. This review aims at a brief but concise overview on the exploitation of ESIPT luminescence for the optimization of DSE dyes properties. In that perspective, a synergistic approach between organic synthesis, fluorescence spectroscopy and ab initio calculations has proven to be an efficient tool for the construction and optimization of DSE-ESIPT fluorophores.

Indexed as

Fluorescent DyesProtonsIonophoresLuminescenceSpectrometry, FluorescenceFluorescent DyesIonophoresProtonsab initio calculationsdual-state emissionESIPT fluorescencefluorophores

Identifiers

PMID35458640
PMCPMC9024454

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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.