Synthesis and spectroscopic properties of β,β′-dibenzo-3,5,8-triaryl-BODIPYs

Abstract

A series of β,β'-bicyclo-3,5-diaryl-BODIPYs were synthesized from the corresponding β,β'-bicyclo-3,5-diiodo-BODIPYs (<b>1a,b</b>) <i>via</i> Pd(0)-mediated Suzuki cross-coupling reactions in 82-92% yields. Subsequent aromatization with DDQ afforded the corresponding β,β'-dibenzo-aryl-BODIPYs, which showed red-shifted absorptions and emissions in the near-IR range. The dibenzo-appended BODIPYs showed characteristic ¹H-, ¹³C-, ¹¹B- and ¹⁹F-NMR shifts, and nearly planar conformations by X-ray crystallography.