An Electron-Accepting aza-BODIPY-Based Donor-Acceptor-Donor Architecture for Bright NIR Emission

A bright near-infrared (NIR) fluorescent molecule was developed based on the donor-acceptor-donor (D-A-D) approach using an aza-BODIPY analog called pyrrolopyrrole aza-BODIPY (PPAB) as an electron-accepting chromophore. Directly introducing electron-donating triphenylamine (TPA) to develop a D-A-D structure caused redshifts of absorption and emission of PPAB into the NIR region with an enhanced fluorescence brightness of up to 5.2x10(4) m(-1) cm(-1), whereas inserting a phenylene linker between the TPA donor and the PPAB acceptor induced solvatochromic behavior in emission. Transient absorption spectra and theoretical calculations revealed the presence of a highly emissive hybridized locally excited and charge-transfer state in the former case and the contribution of the dark charge-separated state to the excited state in the latter case. The bright D-A-D PPAB as a novel emitter resulted in a NIR electroluminescence with a high external quantum efficiency of 3.7 % and a low amplified spontaneous emission threshold of ca. 80 mu J cm(-2), indicating the high potential for NIR optoelectronic applications.

Automated summary

A bright NIR fluorescent molecule based on the D-A-D approach using TPA and PPAB showed enhanced performance, with increased brightness and solvatochromic behavior in emission. This novel emitter demonstrated high potential for efficient NIR optoelectronic applications.