| Literature DB >> 29851219 |
Hilmar Reiss1, Lei Ji2, Jie Han3, Silke Koser1, Olena Tverskoy1, Jan Freudenberg1,4, Felix Hinkel1,5, Michael Moos6, Alexandra Friedrich2, Ivo Krummenacher2, Christoph Lambert6, Holger Braunschweig2, Andreas Dreuw3, Todd B Marder2, Uwe H F Bunz1,5.
Abstract
A cyclocondensation of TIPS-ethynyl-substituted diaminoarenes with in situ obtained 4,5-dibromocyclohexa-3,5-diene-1,2-dione has led to the synthesis of tetrabromotetraazapentacene (BrTAP). BrTAP is easily reduced to its air-stable radical anion and electron mobilities >0.56 cm2 V-1 s-1 can be achieved in thin-film transistors.Entities:
Keywords: azaacenes; bromination; n-channel semiconductors; radical anions; thin-film transistors
Year: 2018 PMID: 29851219 DOI: 10.1002/anie.201805728
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336