Photo-modulation of the two-photon excited fluorescence of dithienylethene bis-(1-pyrenyl) compounds: An experimental and theoretical study

Photomodulation of two-photon excited fluorescence has been effectively controlled in 1-pyrene-based dithienylethenes. The specific molecular design enables photocommutation of two-photon excited fluorescence during sequential one- and two-photon excitations without interference nor destructive optical readout. Theoretical studies have concluded that the internal functionalization of pyrene is responsible for the photoactivity in these systems. Photophysical studies indicate that the presence of a second laterally introduced pyrene is crucial for maintaining high photocommutation contrast and durability. • Synthesis of new unsymmetrical pyrene-based DTE compound. • Photo-control of two-photon excitation signal. • Photo-switchable, all-optical, non-destructive molecular system. • Influence of the position of the pyrenes on the photophysical behavior. • Photo-modulation upon alternation of two- and one-photon excitation.

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Publication Details

Journal
Dyes and Pigments
Published
2024-09-27
DOI
https://doi.org/10.1016/j.dyepig.2024.112473
Citations
5
Primary Topic
Photochromic and Fluorescence Chemistry
Type
article
Field-Weighted Citation Impact
0.59

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article

Photo-modulation of the two-photon excited fluorescence of dithienylethene bis-(1-pyrenyl) compounds: An experimental and theoretical study

Julien Boixel, Elsa Caytan, Muriel Escadeillas, Arnaud Fihey et al.
5 citations
Dyes and Pigments
Photochromic and Fluorescence Chemistry
0.59
article

Photo-modulation of the two-photon excited fluorescence of dithienylethene bis-(1-pyrenyl) compounds: An experimental and theoretical study

Julien Boixel, Elsa Caytan, Muriel Escadeillas, Arnaud Fihey, Grégory Taupier, Yann Molard, Marie Barale, Iulia Turcas, Violette Gousseau
article en
5 citations

Abstract

Photomodulation of two-photon excited fluorescence has been effectively controlled in 1-pyrene-based dithienylethenes. The specific molecular design enables photocommutation of two-photon excited fluorescence during sequential one- and two-photon excitations without interference nor destructive optical readout. Theoretical studies have concluded that the internal functionalization of pyrene is responsible for the photoactivity in these systems. Photophysical studies indicate that the presence of a second laterally introduced pyrene is crucial for maintaining high photocommutation contrast and durability. • Synthesis of new unsymmetrical pyrene-based DTE compound. • Photo-control of two-photon excitation signal. • Photo-switchable, all-optical, non-destructive molecular system. • Influence of the position of the pyrenes on the photophysical behavior. • Photo-modulation upon alternation of two- and one-photon excitation.

Dyes and PigmentsVol. 232
Centre National de la Recherche Scientifique (FR), Université Rennes 2 (FR), Université de Rennes (FR)
Agence Nationale de la Recherche, Centre National de la Recherche Scientifique, Université de Rennes 1, Institut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement
Openalex Percentile: Top 33%
Photochromic and Fluorescence Chemistry
0.59
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