Authors
Jiexi Liang, Chongyang Zeng, Tao Jiang, Xiaohui Wang, Carl Redshaw, Xing Feng
Published in
The Journal of organic chemistry. Jul 16, 2025. Epub Jul 16, 2025.
Abstract
Controllably functionalizing pyrene at specific active sites along the Z-axis remains a significant synthetic challenge. In this work, we present a rationally designed synthetic strategy for the stepwise Z-axis functionalization of pyrene at the 1,3- and 6,8-positions, using a hydroxyl group at the 2-position as a directing group. This approach allows for the construction of novel Z-axis-oriented bipolar pyrene-based molecules. By modulating electron-withdrawing or -donating groups at the 6- and 8-positions, the products demonstrated tunable luminescence ranging from deep blue (426 nm) to orange red (627 nm) with a high fluorescence quantum efficiency.
PMID:
40668984
Bibliographic data and abstract were imported from PubMed on 17 Jul 2025.
Read full publication at:
Please sign in
to see all details.
Advertisement
Stats
- Recommendations n/a n/a positive of 0 vote(s)
- Views 49
- Comments 0