0 Datasets
0 Files
Get instant academic access to this publication’s datasets.
Yes. After verification, you can browse and download datasets at no cost. Some premium assets may require author approval.
Files are stored on encrypted storage. Access is restricted to verified users and all downloads are logged.
Yes, message the author after sign-up to request supplementary files or replication code.
Join 50,000+ researchers worldwide. Get instant access to peer-reviewed datasets, advanced analytics, and global collaboration tools.
✓ Immediate verification • ✓ Free institutional access • ✓ Global collaborationJoin our academic network to download verified datasets and collaborate with researchers worldwide.
Get Free AccessA series of BODIPY derivatives with tetraphenylethene (TPE) moieties were designed and synthesized. The effect of positions and numbers of substitution groups on the fluorescence of the BODIPYs was investigated. Theoretical calculation and single crystal structures proved that the TPE substitution groups on the 8-position of BODIPY contributed little to the conjugation, but benefited the aggregated state emission. On the other hand, the substitutions on the 3- or 5-position of BODIPY through vinyl bridges increased the conjugation length, and generated big coplanar π-conjugated structures with poor aggregated state emission. The compound with bright aggregated state emission has been further fabricated into biocompatible fluorescent nanoparticles and used as effective fluorescent contrast agents for intracellular imaging.
César F. A. Gómez‐Durán, Rongrong Hu, Guangxue Feng, Tingzhong Li, Fan Bu, Mathieu Arseneault, Bin Liu, Eduardo Peña‐Cabrera, Ben Zhong Tang (2015). Effect of AIE Substituents on the Fluorescence of Tetraphenylethene-Containing BODIPY Derivatives. , 7(28), DOI: https://doi.org/10.1021/acsami.5b05033.
Datasets shared by verified academics with rich metadata and previews.
Authors choose access levels; downloads are logged for transparency.
Students and faculty get instant access after verification.
Type
Article
Year
2015
Authors
9
Datasets
0
Total Files
0
Language
en
DOI
https://doi.org/10.1021/acsami.5b05033
Access datasets from 50,000+ researchers worldwide with institutional verification.
Get Free Access
