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Nitrile Substitution Effect on Triphenodioxazine‐Based Materials for Liquid‐Processed Air‐Stable n‐Type Organic Field Effect Transistors
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Citations
36
References
2015
Year
Air-stable MaterialEngineeringOrganic ElectronicsOrganic ChemistryChemistryFavorable Molecular PackingChemical EngineeringNanoelectronicsTriphenodioxazine‐based MaterialsOnline DeliveryOrganic SemiconductorPhysical ChemistryNitrile Substitution EffectOrganic MaterialsOrganic Charge-transfer CompoundOrganic Material ChemistryElectronic MaterialsApplied PhysicsMolecule-based MaterialFunctional Materials
Air-stable material for vacuum or liquid-processed n-type organic field-effect transistors is easily synthesized by cyano-substitutions on para and ortho positions versus nitrogen of soluble triphenodioxazines. This regioisomer promotes favorable molecular packing while increasing the electron affinity. Without encapsulation and after 30 days, the performances of devices remain high under air measurement conditions. As a service to our authors and readers, this journal provides supporting information supplied by the authors. Such materials are peer reviewed and may be re-organized for online delivery, but are not copy-edited or typeset. Technical support issues arising from supporting information (other than missing files) should be addressed to the authors. Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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