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      Hetero‐Substituted αβ‐Fused BODIPY

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          Abstract

          Here, we report the synthesis and properties of heterosubtituted αβ‐fused BODIPY fluorophores. The compounds were obtained in good yields by sequential and selective Stille cross‐coupling reactions from 2,3,5,6‐tetrahalo‐BODIPY, allowing the introduction of different substituents at the 3,5 and 2,6 positions of the BODIPY ring. The final fused compounds were synthesized using oxidative cyclisation with ferrous chloride. The fully fused compounds show a strong bathochromically shifted emission along with a hyperchromic shift of the absorption maxima. The fluorescence quantum yields remain relatively large for compounds emitting in this wavelength range. Computational studies have been carried out to fully understand the photophysical behaviour of these dyes.

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          The chemistry of fluorescent bodipy dyes: versatility unsurpassed.

          The world of organic luminophores has been confined for a long time to fairly standard biological labeling applications and to certain analytical tests. Recently, however, the field has undergone a major change of direction, driven by the dual needs to develop novel organic electronic materials and to fuel the rapidly emerging nanotechnologies. Among the many diverse fluorescent molecules, the Bodipy family, first developed as luminescent tags and laser dyes, has become a cornerstone for these new applications. The near future looks extremely bright for "porphyrin's little sister".
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            Nonfullerene Acceptor Molecules for Bulk Heterojunction Organic Solar Cells

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              BODIPY dyes and their derivatives: syntheses and spectroscopic properties.

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                Author and article information

                Contributors
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                Journal
                Chemistry – A European Journal
                Chemistry A European J
                Wiley
                0947-6539
                1521-3765
                May 02 2022
                March 23 2022
                May 02 2022
                : 28
                : 25
                Affiliations
                [1 ] Institut de Chimie et Procédés pour l'Énergie l'Environnement et la Santé (ICPEES), UMR CNRS 7515 École Européenne de Chimie, Polymères et Matériaux (ECPM) 25 Rue Becquerel 67087 Strasbourg Cedex 02 France
                [2 ] Université de Nantes, CEISAM UMR 6230, CNRS 44000 Nantes France
                Article
                10.1002/chem.202200130
                f2f8ac20-f412-4349-bdb4-77336344a732
                © 2022

                http://onlinelibrary.wiley.com/termsAndConditions#vor

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