Angewandte Chemie International Edition · 2015 · 157 citations · 50 references
Natural SciencesChemistryMaterials ScienceOrganic ChemistrySemiconductor DevicesSemiconductor MaterialsHeterocycle SynthesisHeterocyclic ChemistryHeterocyclic CompoundsOrganic Electronic MaterialsOrganic SemiconductorsOrganic SynthesisAromatic HeterocyclesElectron MobilityHeterocycle FunctionalizationHeterocyclic AromaticityHeterocyclic MaterialsHigh-electron-mobility TransistorsOrganic Electronics
Increasing the length of N-heteroacenes or their analogues is highly desirable because such materials could have great potential applications in organic electronics. In this report, the large π-conjugated N-heteroquinone 6,10,17,21-tetra-((triisopropylsilyl)ethynyl)-5,7,9,11,16,18,20,22-octaazanonacene-8,19-dione (OANQ) has been synthesized and characterized. The as-prepared OANQ shows high stability under ambient conditions and has a particularly low LUMO level, which leads to it being a promising candidate for air-stable n-type field-effect transistors (FETs). In fact, FET devices based on OANQ single crystals have been fabricated and an electron mobility of up to 0.2 cm(2) V(-1) s(-1) under ambient conditions is reported. More importantly, no obvious degradation was observed even after one month. Theoretical calculations based on the single crystal are consistent with the measured mobility.
50
Electron transfer reactions in chemistry. Theory and experiment
R. A. Marcus · Reviews of Modern Physics · 1993 · 3.6K citations · Full text
n‐Type Organic Semiconductors in Organic Electronics
John E. Anthony, Antonio Facchetti, Martin Heeney et al. · Advanced Materials · 2010 · 1.2K citations