Brosius, Victor
[VerfasserIn];
Weigold, Svenja
[VerfasserIn];
Hippchen, Nikolai
[VerfasserIn];
Rominger, Frank
[VerfasserIn];
Freudenberg, Jan
[VerfasserIn];
Bunz, Uwe H. F.
[VerfasserIn]
Beschreibung:
The syntheses, properties and application of the air-stable electron acceptors, diindenopyrazines 4 a-g are reported demonstrating the introduction of functional aryl groups in the 6- and 12-positions. The targets are accessible on the hundred milligram to gram scale. The structure of the aryl groups in 4 a-g modulates their solubility, redox potentials and optical properties. The introduction of electron-poor aryl groups to the electron-poor diindenopyrazine backbone reduces the electron affinity to −4 eV, making the compounds attractive as n-semiconductors. A simple organic field-effect transistor of 4 e -without optimization- shows electron transport with a mobility of up to 0.037 cm2 V−1 s−1.