J-aggregation induced emission enhancement of BODIPY dyes via H-bonding directed supramolecular polymerization: the importance of substituents at boron
Abstract
For uracil-functionalized BODIPY dyes 1a–c , AIEE upon H-bonding directed J-aggregation was observed for the two dyes bearing alkyne groups at boron while the BF 2 -chelated dye displayed ACQ, indicating the crucial role of the substituents at boron.
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Substituent effects on the supramolecular polymerization of 5,15-dioxaporphyrin
Duan, R., Iwasaki, T., & Shimizu, S. (2026) · Chemistry Letters · doi:10.1093/chemle/upag155
- Authors
- Zhang, Y., Yuan, S., Liu, P., Jing, L., Pan, H., Ren, X.-K., & Chen, Z.
- Affiliations
- Tianjin University (CN)
- Corresponding author
- Ren, Xiang-Kui
- Chen, Zhijian
- Venue
- Organic Chemistry Frontiers
- Publisher
- Royal Society of Chemistry (RSC)
- Published
- 2021
- Volume
- 8
- Issue
- 15
- Pages
- 4078-4085
- ISSN
- 2052-4110 (ISSN-L)
- 2052-4129
- OpenAlex
- W3164434676
- Cited by
- 58
- References
- 49
- Citations by year
- 2026: 7 · 2025: 9 · 2024: 12 · 2023: 14 · 2022: 13 · 2021: 3
- FWCI
- 3.19
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Organic Chemistry Frontiers (publishedVersion)
- Funders
- National Natural Science Foundation of China (21875157, 92056115)
- Topics
- Physical Sciences › Materials Science › Materials Chemistry › Luminescence and Fluorescent Materials
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Photochemistry and Electron Transfer Studies
- Physical Sciences › Chemistry › Spectroscopy › Molecular Sensors and Ion Detection
- Keywords
- aggregation-induced emission enhancement, J-aggregation, BODIPY dyes, aggregation-caused quenching, supramolecular polymers
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