Improving the Stability of Organic Semiconductors: Distortion Energy versus Aromaticity in Substituted Bistetracene

Keyphrases

• Organic Semiconductors 100%
• Aromaticity 100%
• Distortion Power 100%
• Bistetracene 100%
• Polycyclic Aromatic Hydrocarbons 50%
• Pentacene 50%
• Rubrene 50%
• Order of Magnitude 33%
• Photooxidation 33%
• Density Functional Theory 16%
• Cycloaddition 16%
• Activation Barrier 16%
• Reaction Mechanism 16%
• Electron Paramagnetic Resonance Spectroscopy 16%
• Enhanced Stability 16%
• Electron Transfer 16%
• Molecular Oxygen 16%
• Recombination Mechanism 16%
• Field-effect Transistors 16%
• Oxidation Reaction 16%
• Computational Results 16%
• Organic Electronic Devices 16%
• Solar Cell 16%
• Small Distortion 16%
• Endoperoxide 16%
• NMR Analysis 16%
• Diels-Alder 16%
• Molecular Semiconductors 16%
• Charge Recombination 16%
• Charged Species 16%
• Trimethylsilyl 16%
• Reactions in Solution 16%
• Ethynyl 16%
• Photooxidation Reaction 16%
• High Charge Carrier Mobility 16%

Chemistry

• Pentacene 100%
• Polycyclic Aromatic Hydrocarbons 100%
• Photooxidation 100%
• Density Functional Theory 33%
• NMR Spectroscopy 33%
• EPR Spectroscopy 33%
• Oxidation Reaction 33%
• Electron Transport 33%
• Charge Carrier 33%
• Dioxygen 33%
• Field Effect 33%
• Ethynyl 33%
• Solar Cell 33%
• Diels-Alder Cycloaddition 33%