| Literature DB >> 33475384 |
Philipp Rietsch1, Mohammad Zeyat2, Oskar Hübner3, Katrin Hoffmann3, Maximilian Kutter2, Alice Paskin2, Julian Uhlig2, Dieter Lentz2, Ute Resch-Genger3, Siegfried Eigler1.
Abstract
The absorption and emission properties of organic dyes are generally tuned by altering the substitution pattern. However, tuning the fluorescence lifetimes over a range of several 10 ns while barely affecting the spectral features and maintaining a moderate fluorescence quantum yield is challenging. Such properties are required for lifetime multiplexing and barcoding applications. Here, we show how this can be achieved for the class of fluoranthene dyes, which have substitution-dependent lifetimes between 6 and 33 ns for single wavelength excitation and emission. We explore the substitution-dependent emissive properties in the crystalline solid state that would prevent applications. Furthermore, by analyzing dye mixtures and embedding the dyes in carboxy-functionalized 8 μm-sized polystyrene particles, the unprecedented potential of these dyes as labels and encoding fluorophores for time-resolved fluorescence detection techniques is demonstrated.Entities:
Year: 2021 PMID: 33475384 DOI: 10.1021/acs.jpcb.0c08851
Source DB: PubMed Journal: J Phys Chem B ISSN: 1520-5207 Impact factor: 2.991