Login / Signup

Catalytic aerobic photooxidation of triarylphosphines using dibenzo-fused 1,4-azaborines.

Masaru KondoTomohiro Agou
Published in: Chemical communications (Cambridge, England) (2022)
Although dibenzo-fused 1,4-heteroaromatics are utilized as strongly reducing photocatalysts in organic synthesis and polymerization, they have rarely been employed in catalytic photooxidation. Moreover, to date, their boron-analogs, dibenzo-fused 1,4-azaborines (DBABs), have not been applied in photocatalysis despite their promising potential as photocatalysts. Accordingly, herein, aerobic photooxidation of triarylphosphines (Ar 3 P) was performed using DBABs as photocatalysts. The reaction smoothly proceeded in an aprotic solvent, and phosphine oxides were obtained in appropriate yields. Density functional theory calculations suggested that DBAB captured and activated phosphadioxirane intermediates, which were generated by the interaction of Ar 3 P with 1 O 2 , at the Lewis acidic boron center.
Keyphrases
  • density functional theory
  • visible light
  • ionic liquid
  • molecular dynamics
  • high intensity
  • molecular docking
  • crystal structure
  • molecular dynamics simulations