Revisiting the synthesis of the benzothioxanthene imide five decades later
Author:
Affiliation:
1. Univ Angers, CNRS, MOLTECH-ANJOU, SFR MATRIX, F-49000 Angers, France
2. Univ Rennes, CNRS UMR6226, F-3500 Rennes, France
3. Building Blocks for FUture Electronics Laboratory (2BFUEL), IRL2002, CNRS-Yonsei University, Seoul, South Korea
Abstract
Funder
Agence Nationale de la Recherche
Centre National de la Recherche Scientifique
Publisher
Royal Society of Chemistry (RSC)
Subject
Materials Chemistry,General Chemistry,Catalysis
Link
http://pubs.rsc.org/en/content/articlepdf/2022/NJ/D2NJ00955B
Reference9 articles.
1. Heterocyclic derivalives of naphthalene-1,8-dicar boxylie anhydride. Part III. Benzo[k,l] thioxanthene-3,4-dicarboximides
2. A new intramolecular cyclisation reaction—I
3. Bromination of the benzothioxanthene Bloc: toward new π-conjugated systems for organic electronic applications
4. Synthesis, characterization and use of benzothioxanthene imide based dimers
5. Ternary organic solar cells: using molecular donor or acceptor third components to increase open circuit voltage
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