4.8 Article

Bromination Improves the Electron Mobility of Tetraazapentacene

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 57, 期 30, 页码 9543-9547

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201805728

关键词

azaacenes; bromination; n-channel semiconductors; radical anions; thin-film transistors

资金

  1. Deutsche Forschungsgemeinschaft [SFB 1249, GRK 2112]
  2. Julius-Maximilians-Universitat Wurzburg
  3. Chinese Scholarship Council [201406170060]
  4. Bavarian State Ministry of Science, Research, and the Arts (Collaborative Research Network Solar Technologies Go Hybrid)

向作者/读者索取更多资源

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 cm(2) V-1 s(-1) can be achieved in thin-film transistors.

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