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| Naji, M. |
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| Motta, Antonella |
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| Aletan, Dirar |
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| Mohamed, Tarek |
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| Ertürk, Emre |
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| Taccardi, Nicola |
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| Kononenko, Denys |
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| Petrov, R. H. | Madrid |
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| Alshaaer, Mazen | Brussels |
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| Bih, L. |
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| Casati, R. |
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| Muller, Hermance |
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| Kočí, Jan | Prague |
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| Šuljagić, Marija |
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| Kalteremidou, Kalliopi-Artemi | Brussels |
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| Azam, Siraj |
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| Ospanova, Alyiya |
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| Blanpain, Bart |
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| Ali, M. A. |
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| Popa, V. |
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| Rančić, M. |
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| Ollier, Nadège |
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| Azevedo, Nuno Monteiro |
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| Landes, Michael |
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| Rignanese, Gian-Marco |
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Marszalek, Tomasz
in Cooperation with on an Cooperation-Score of 37%
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Publications (5/5 displayed)
- 2024Role of Meniscus Shape on Crystallization of Molecular Semiconductors and Fluid Dynamics During Meniscus‐Guided Coatingcitations
- 2023Modification of Two‐Dimensional Tin‐Based Perovskites by Pentanoic Acid for Improved Performance of Field‐Effect Transistorscitations
- 20195,7,12,14‐Tetrafunctionalized 6,13‐Diazapentacenescitations
- 2019Impact of polymorphism on the optoelectronic properties of a low-bandgap semiconducting polymercitations
- 2017Controlled molecular orientation of inkjet printed semiconducting polymer fibers by crystallization templatingcitations
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article
5,7,12,14‐Tetrafunctionalized 6,13‐Diazapentacenes
Abstract
<jats:title>Abstract</jats:title><jats:p>The synthesis, property evaluation, and single crystal X‐ray structures of four 5,7,12,14‐tetrafunctionalized diazapentacenes are presented. The synthesis of these compounds either starts from tetrabromo‐<jats:italic>N</jats:italic>,<jats:italic>N</jats:italic>‐dihydrodiazapentacene or from a diazapentacene tetraketone. Pd‐catalyzed coupling or addition of a lithium acetylide gave the precursors that furnish, after further redox reactions, the diazapentacenes as stable crystalline materials. The performance of the tetraphenyl‐substituted compound as n‐channel semiconductor was evaluated in organic field effect transistors.</jats:p>