posted on 2016-02-04, 15:59authored bySho Yamazawa, Mika Nakashima, Yukie Suda, Ryuhei Nishiyabu, Yuji Kubo
2,3-Naphtho-fused
boron-dipyrromethenes (BODIPYs) 1a and 1b, which absorb near-infrared light at 740–770
nm with molar extinction coefficients above 105 M–1 cm–1 in THF, have been synthesized through a palladium(II)-catalyzed
direct acylation of N-BOC hydrazones and subsequent
Paal–Knorr pyrrole synthesis. Simple benzo-annulation of dibenzo-BODIPY
caused a significant red-shift in the absorption. Subsequent intramolecular B,O-cyclization of 1b gave 2, which exhibited an intense absorption band at 830 nm. The
structure–optical property relationship has been investigated
using theoretical calculations and cyclic voltammetry.