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Synthesis of indano[60]fullerene thioketone and its application in organic solar cells.

Yong-Chang ZhaiShimon OiwaShinobu AoyagiShohei OhnoTsubasa MikieJun-Zhuo WangHirofumi AmadaKoki YamanakaKazuhira MiwaNaoyuki ImaiTakeshi IgarashiItaru OsakaYutaka Matsuo
Published in: Beilstein journal of organic chemistry (2024)
Evaporable indano[60]fullerene ketone (FIDO) was converted to indano[60]fullerene thioketone (FIDS) in high yield by using Lawesson's reagent. Three compounds with different substituents in para position were successfully converted to the corresponding thioketones, showing that the reaction tolerates compounds with electron-donating and electron-withdrawing substituents. Computational studies with density functional theory revealed the unique vibrations of the thioketone group in FIDS. The molecular structure of FIDS was confirmed by single-crystal X-ray analysis. Bulk heterojunction organic solar cells using three evaporable fullerene derivatives (FIDO, FIDS, C 60 ) as electron-acceptors were compared, and the open-circuit voltage with FIDS was 0.16 V higher than that with C 60 .
Keyphrases
  • solar cells
  • density functional theory
  • molecular dynamics
  • high resolution
  • minimally invasive
  • water soluble
  • computed tomography
  • magnetic resonance
  • case control
  • mass spectrometry