Solubility and Crystallizability: Facile Access to Functionalized π‐Conjugated Compounds with Chlorendylimide Protecting Groups |
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| Authors: | Dr Jan Gebers Damien Rolland Dr Roman Marty Dr Stéphane Suàrez Luca Cervini Dr Rosario Scopelliti Dr Jan Cornelius Brauer Prof Dr Holger Frauenrath |
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| Affiliation: | 1. Institute of Materials, école Polytechnique Fédérale de Lausanne (EPFL), EPFL–STI–IMX–LMOM, MXG 037, Station 12, 1015 Lausanne (Switzerland), Fax: (+41)?21‐69‐35270;2. Institute of Chemical Science and Engineering, école Polytechnique Fédérale de Lausanne (EPFL) |
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| Abstract: | Functional π‐conjugated molecules are relevant for the preparation of new organic electronic materials with improved performance. However, their synthesis is often rendered difficult by their inherently low solubility, and the permanent attachment of solubilizing groups may change the properties of the material. Here, we introduced the chlorendylimidyl moiety as a new temporary protecting group for the straightforward large‐scale synthesis of protected quarter‐, sexi‐, octathiophene, and perylene bisimide diamine and dicarboxylic acid derivatives. The obtained chlorendylimides and chlorendylimidyl active esters were highly soluble in organic solvents, and optical spectroscopy confirmed the low tendency of the compounds to aggregate in solution. At the same time, they could be conveniently purified by recrystallization or precipitation. Single‐crystal X‐ray structures obtained for most compounds showed supramolecular motifs highlighting the role of the rigid, polychlorinated chlorendyl moieties in their crystallization. The obtained protected diamine and dicarboxylic acid derivatives were easily deprotected and converted into various amide‐substituted oligothiophenes and perylene bisimides that are of interest as new functional materials for organic electronic thin film or nanowire devices. |
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| Keywords: | functional molecules polymers protecting groups supramolecular chemistry synthetic methods |
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