Fluorescence modulation by fast photochromism ...
Document type :
Article dans une revue scientifique: Article original
DOI :
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Title :
Fluorescence modulation by fast photochromism of a [2.2]paracyclophane-bridged imidazole dimer possessing a perylene bisimide moiety
Author(s) :
Mutoh, Katsuya [Auteur]
Aoyama Gakuin University [AGU]
Sliwa, Michel [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 [LASIRE]
Fron, Eduard [Auteur]
Catholic University of Leuven = Katholieke Universiteit Leuven [KU Leuven]
Hofkens, Johan [Auteur]
Catholic University of Leuven = Katholieke Universiteit Leuven [KU Leuven]
Abe, Jiro [Auteur]
Aoyama Gakuin University [AGU]
Aoyama Gakuin University [AGU]
Sliwa, Michel [Auteur]
Laboratoire Avancé de Spectroscopie pour les Intéractions la Réactivité et l'Environnement - UMR 8516 [LASIRE]
Fron, Eduard [Auteur]
Catholic University of Leuven = Katholieke Universiteit Leuven [KU Leuven]
Hofkens, Johan [Auteur]
Catholic University of Leuven = Katholieke Universiteit Leuven [KU Leuven]
Abe, Jiro [Auteur]
Aoyama Gakuin University [AGU]
Journal title :
Journal of Materials Chemistry C
Volume number :
6
Pages :
9523-9531
Publication date :
2018
HAL domain(s) :
Chimie/Chimie théorique et/ou physique
English abstract : [en]
The development of single-molecule imaging and super-resolution microscopy techniques has promoted the study of fluorescence switchable molecules that have been important for the in-depth understanding of the activities ...
Show more >The development of single-molecule imaging and super-resolution microscopy techniques has promoted the study of fluorescence switchable molecules that have been important for the in-depth understanding of the activities of organelles and the geometries of materials in the nano- and microscale. The utilization of photochromic compounds as the photo-switching trigger is an efficient strategy to reversibly control the fluorescent “ON” and “OFF” states. In this study, we demonstrated the red-color fluorescence switching of a perylene bisimide (PBI) derivative by using a fast photochromic [2.2]paracyclophane-bridged imidazole dimer. The transient colored biradical species as the fluorescence quencher is generated upon UV light irradiation. Because the biradical species has broad absorption bands in the whole visible light and the near-infrared regions (500–900 nm), the fluorescence of PBI could be efficiently quenched by Förster resonance energy transfer (FRET). The fluorescence intensity was switched by means of fast photochromic cycles within a few tens of milliseconds. The potential capability of the transient biradical species to switch the fluorescence in the visible and NIR regions will open up new possibilities in multicolor fluorescence imaging.Show less >
Show more >The development of single-molecule imaging and super-resolution microscopy techniques has promoted the study of fluorescence switchable molecules that have been important for the in-depth understanding of the activities of organelles and the geometries of materials in the nano- and microscale. The utilization of photochromic compounds as the photo-switching trigger is an efficient strategy to reversibly control the fluorescent “ON” and “OFF” states. In this study, we demonstrated the red-color fluorescence switching of a perylene bisimide (PBI) derivative by using a fast photochromic [2.2]paracyclophane-bridged imidazole dimer. The transient colored biradical species as the fluorescence quencher is generated upon UV light irradiation. Because the biradical species has broad absorption bands in the whole visible light and the near-infrared regions (500–900 nm), the fluorescence of PBI could be efficiently quenched by Förster resonance energy transfer (FRET). The fluorescence intensity was switched by means of fast photochromic cycles within a few tens of milliseconds. The potential capability of the transient biradical species to switch the fluorescence in the visible and NIR regions will open up new possibilities in multicolor fluorescence imaging.Show less >
Language :
Anglais
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
CNRS
ENSCL
Université de Lille
ENSCL
Université de Lille
Collections :
Research team(s) :
Dynamics, Nanoscopy & Chemometrics (DyNaChem)
Submission date :
2021-11-16T08:23:30Z
2024-02-21T12:49:02Z
2024-02-21T12:49:02Z