π-Conjugation Engineering of Isoindolinone-Based Aryl Amides Enables Highly Efficient Fluorescence via Control of Nonradiative Pathways
Clicks: 5
ID: 317127
2026
Article Quality & Performance Metrics
Overall Quality
Not rated
Combines reader engagement with the AI quality analysis. This
article has not been analysed, so there is no overall score —
reader engagement is measured and shown alongside.
Reader Engagement
Emerging Content
1.2
/100
5 views
4 readers
AI Quality Assessment
Not analyzed
Readership in this journal
EmergingRanked #782 of 793 articles by views in phytochemistry letters
Most read
Least read
Bar heights use a square-root scale. Only the 120 most-read articles are drawn; the journal has 793 in total.
Mint this article as an NFT
Not yet mintedCreate a permanent, verifiable on-chain record of this article on the Scimatic Network. The NFT is held in your Journament account, and you can withdraw it to your own wallet at any time.
5
SUSD
one-off · no wallet required
Abstract
Abstract π-Conjugation extension in N-aryl isoindolinones enables rational control of excited-state pathways and fluorescence efficiency. Stepwise π-extension enhances fluorescence quantum yield from 0.04 to 0.58 while maintaining large Stokes shifts. Photophysical measurements and theoretical calculations suggest that the enhanced fluorescence efficiency is associated with modulation of excited-state pathways, including reduced ISC probability and TICT-like structural relaxation. These findings indicate that the isoindolinone framework provides a versatile platform for designing highly emissive chromophores through precise control of excited-state dynamics.
| Reference Key |
openalex_W7164501379
Use this key to autocite in the manuscript while using
SciMatic Manuscript Manager or Thesis Manager
|
|---|---|
| Authors | Yuki Sawatari, Takuya Tanaka, Isao Azumaya, Toshifumi Mori, Gen‐ichi Konishi |
| Journal | phytochemistry letters |
| Year | 2026 |
| DOI |
10.1093/chemle/upag123
|
| URL | |
| Keywords | Keywords not found |
Citations
No citations found. To add a citation, contact the admin at info@scimatic.org
Comments
No comments yet. Be the first to comment on this article.