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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.
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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