Flexible graphene paper for large-scale electroorganic synthesis: C–H amination of benzoxazole derivatives


Dağalan Z., Aksu Z., ÇELİKOĞLU M. H., ERÇARIKCI E., DAĞCI KIRANŞAN K., ALANYALIOĞLU M., ...Daha Fazla

Reaction Chemistry and Engineering, 2026 (SCI-Expanded, Scopus) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Basım Tarihi: 2026
  • Doi Numarası: 10.1039/d5re00512d
  • Dergi Adı: Reaction Chemistry and Engineering
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Chemical Abstracts Core, Compendex
  • Atatürk Üniversitesi Adresli: Evet

Özet

Large-scale synthesis of organic compounds using electrochemistry is an emerging, green, and sustainable approach, as it reduces the need for harsh chemicals, potentially lowers energy consumption, and minimizes waste. The C–H amination reactions are important because of the direct transformation of inert C–H bonds into more efficient and selective C–N bonds. This reaction also helps streamline synthetic routes by reducing the number of steps and the need for protecting groups. For large-scale electrochemical C–H amination reactions, the best way is to increase the electrode surface area. However, this approach is a big challenge with classical electrodes, e.g., glassy carbon electrode (GCE). New-type flexible, rollable, and durable electrodes are required to overcome this challenge. This work reports the production of a flexible graphene-based paper electrode (FGPE) using an economic mold-casting method for large-scale electrochemical C–H amination reactions of various benzoxazole derivatives. For the characterization of FGPEs and products of electroorganic synthesis, we have performed numerous advanced techniques. We have determined that C–H amination reactions occur with yields of at least 95% in 13 h by bending the FGPE. Large-scale electrochemical synthesis applications were applied using 5 times more electrode surface area of the FGPE, leveraging its flexibility and foldability. They exhibited a yield of 90% with a 16.7-fold increase in benzoxazole amount in the cell.