| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 10588137 | Bioorganic & Medicinal Chemistry Letters | 2012 | 4 Pages |
Abstract
Variation at the 3' position of fluorescein via Suzuki-Miyaura cross-coupling with aryl and heteroaryl moieties gave a family of anthofluoresceins whose spectroscopic properties were studied. The 1-methylindole derivative gave the highest quantum yield and was observed to behave as a molecular rotor, displaying marked variations in fluorescent intensities with viscosity and offering possible application in cellular sensing and fluorescent polarisation assays.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Rahimi M. Yusop, Asier Unciti-Broceta, Mark Bradley,