4.7 Article

The rapid construction of bis-BN dipyrrolyl[a,j]anthracenes and a direct comparison with a carbonaceous analogue

Journal

ORGANIC CHEMISTRY FRONTIERS
Volume 9, Issue 12, Pages 3328-3334

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2qo00083k

Keywords

-

Funding

  1. National Natural Science Foundation of China [22071181]
  2. Natural Science Foundation of Tianjin [17JCZDJC37700, 18JCYBJC86100, 18JCQNJC06900]
  3. Tianjin University of Technology
  4. Training Project of Innovation Team of Colleges and Universities in Tianjin [TD13-5020]

Ask authors/readers for more resources

In this study, a series of bis-BN dipyrrolyl[a,j]anthracenes and a carbonaceous analogue were successfully synthesized. The bis-BN dipyrrolyl[a,j]anthracenes exhibited stronger fluorescence and blue-shifted absorption and emission spectra compared to the carbonaceous analogue. Furthermore, organic light-emitting diodes based on these compounds showed high efficiency and pure-blue emitting color.
A series of bis-BN dipyrrolyl[a,j]anthracenes and one of their representative carbonaceous analogues have been synthesized in a short number of steps. Bis-BN dipyrrolyl[a,j]anthracenes are strongly fluorescent in solution. Both the absorption and emission spectra of bis-BN dipyrrolyl[a,j]anthracenes are blue shifted compared to the carbonaceous analogue. Moreover, organic light-emitting diodes based on these compounds were fabricated via a solution method. In particular, device II with 4b as an emitter presents a pure-blue emitting color with a high current efficiency (3.84 cd A(-1)) and CIE coordinates of (0.18, 0.21), whereas device VII based on the carbonaceous analogue displays yellowish-green luminescence with lower efficiency.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available