Single molecule aggregation-induced dual and white-light emissive etherified aroyl- S , N -ketene acetals via one-pot synthesis.
| Autor: | Biesen L; Institut für Organische Chemie und Makromolekulare Chemie, Heinrich-Heine-Universität Düsseldorf Universitätsstraße 1 D-40225 Düsseldorf Germany ThomasJJ.Mueller@hhu.de., Müller TJJ; Institut für Organische Chemie und Makromolekulare Chemie, Heinrich-Heine-Universität Düsseldorf Universitätsstraße 1 D-40225 Düsseldorf Germany ThomasJJ.Mueller@hhu.de. |
|---|---|
| Jazyk: | angličtina |
| Zdroj: | RSC advances [RSC Adv] 2023 Jun 05; Vol. 13 (25), pp. 16867-16871. Date of Electronic Publication: 2023 Jun 05 (Print Publication: 2023). |
| DOI: | 10.1039/d3ra02935b |
| Abstrakt: | Etherified aroyl- S , N -ketene acetals are readily synthesized by a novel one-pot addition-elimination-Williamson-etherification sequence. Although the underlying chromophore remains constant, derivatives show pronounced color-tuning of solid-state emission and AIE characteristics, whereas a hydroxy-methyl derivative represents an easily accessible mono molecular aggregation-induced white-light emitter. Competing Interests: There are no conflicts to declare. (This journal is © The Royal Society of Chemistry.) |
| Databáze: | MEDLINE |
| Externí odkaz: |
|