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Diindeno[1,2-b:2′,1′-n]perylene: a closed shell related Chichibabin's hydrocarbon, the synthesis, molecular packing, electronic and charge transport properties

Diindeno[1,2-b:2′,1′-n]perylene, a new derivative of the indenoacene family was synthesized, and its electronic, electrochemical, and electrical properties were investigated. This material has a closed shell electronic configuration which corresponds to a quinoidal structure with a low band gap of 1...

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Detalles Bibliográficos
Autores principales: Sbargoud, Kamal, Mamada, Masashi, Marrot, Jérôme, Tokito, Shizuo, Yassar, Abderrahim, Frigoli, Michel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5659070/
https://www.ncbi.nlm.nih.gov/pubmed/29511505
http://dx.doi.org/10.1039/c5sc00652j
Descripción
Sumario:Diindeno[1,2-b:2′,1′-n]perylene, a new derivative of the indenoacene family was synthesized, and its electronic, electrochemical, and electrical properties were investigated. This material has a closed shell electronic configuration which corresponds to a quinoidal structure with a low band gap of 1.35 eV. Molecular packing in the single crystal was studied by single-crystal X-ray structural analysis, and this information was subsequently used in the determination of the charge transfer integrals via density functional theory methods. The charge-carrier transport properties of the diindeno[1,2-b:2′,1′-n]perylene-5,12-dione and diindeno[1,2-b:2′,1′-n]perylene derivatives were investigated through the fabrication and characterization of field-effect transistors via both vacuum-deposited and solution-processed films, respectively. Diindeno[1,2-b:2′,1′-n]perylene exhibited a field-effect behaviour with a hole mobility up to 1.7 × 10(–3) cm(2) V(–1) s(–1) when the active layer was solution-processed.