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Direct alkylthio-functionalization of unsubstituted perylenediimides
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Title: Direct alkylthio-functionalization of unsubstituted perylenediimides |
Authors: Zink Lorre, Nathalie  Font-Sanchis, Enrique  Sastre-Santos, Ángela  Fernández-Lázaro, Fernando  |
Editor: Royal Society of Chemistry |
Department: Departamentos de la UMH::Farmacología, Pediatría y Química Orgánica |
Issue Date: 2016-10 |
URI: https://hdl.handle.net/11000/38041 |
Abstract:
Herein, we report a simple fluoride-mediated reaction for the direct mono- and dialkylthio-functionalization
of unsubstituted perylenediimides (PDIs) under very mild conditions. The aromatic substitution
reaction offers the possibility to introduce primary, secondary and, even, tertiary alkanethiols either on
the 1- or on the 1,6-bay positions of unsubstituted PDIs. 1,6-DialkylthioPDIs show that absorption and
fluorescence spectra shifted to the red when compared with the unsubstituted PDI, with Stokes shifts
around 70–80 nm.
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Keywords/Subjects: Alkylthio-functionalization Perylenediimides (PDIs) Fluoride-mediated reaction Aromatic substitution |
Type of document: info:eu-repo/semantics/article |
Access rights: info:eu-repo/semantics/closedAccess Attribution-NonCommercial-NoDerivatives 4.0 Internacional |
DOI: https://doi.org/10.1039/c6ob01536k |
Published in: Organic & Biomolecular Chemistry. 2016 Oct 4;14(39):9375-9383 |
Appears in Collections: Artículos Farmacología, Pediatría y Química Orgánica
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