Beilstein Journal of Organic Chemistry (Mar 2020)

Six-fold C–H borylation of hexa-peri-hexabenzocoronene

  • Mai Nagase,
  • Kenta Kato,
  • Akiko Yagi,
  • Yasutomo Segawa,
  • Kenichiro Itami

DOI
https://doi.org/10.3762/bjoc.16.37
Journal volume & issue
Vol. 16, no. 1
pp. 391 – 397

Abstract

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Hexa-peri-hexabenzocoronene (HBC) is known to be a poorly soluble polycyclic aromatic hydrocarbon for which direct functionalization methods have been very limited. Herein, the synthesis of hexaborylated HBC from unsubstituted HBC is described. Iridium-catalyzed six-fold C–H borylation of HBC was successfully achieved by screening solvents. The crystal structure of hexaborylated HBC was confirmed via X-ray crystallography. Optoelectronic properties of the thus-obtained hexaborylated HBC were analyzed with the support of density functional theory calculations. The spectra revealed a bathochromic shift of absorption bands compared with unsubstituted HBC under the effect of the σ-donation of boryl groups.

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