| Literature DB >> 33830516 |
Victor Brosius1, Svenja Weigold1, Nikolai Hippchen1, Frank Rominger1, Jan Freudenberg1, Uwe H F Bunz1.
Abstract
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 .Entities:
Keywords: electron acceptors; organic field effect transistors; quinoidal heteroaromatics; semiconductor; synthetic methods
Year: 2021 PMID: 33830516 DOI: 10.1002/chem.202100372
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236