Sato Kazuyuki, Kawasaki Akira, Karuo Yukiko, Tarui Atsushi, Kawai Kentaro, Omote Masaaki
Faculty of Pharmaceutical Sciences, Setsunan University, 45-1 Nagaotoge-cho, Hirakata, Osaka 573-0101, Japan.
Beilstein J Org Chem. 2020 Jun 22;16:1411-1417. doi: 10.3762/bjoc.16.117. eCollection 2020.
Fluorescent molecules based on a fluorinated isoxazole scaffold were synthesized and investigated for their photochemical properties. The introduction of a fluorine substituent into 3,5-diarylisoxazoles led to an increase of fluorescence intensity and exhibited a redshift in the emission intensity. α-Fluorinated boron ketoiminates (F-BKIs) were also synthesized via a ring-opening reaction of 4-fluoroisoxazoles and exhibited highly fluorescent luminescence and aggregation-induced emission (AIE), showing promise as a new fluorophore.
合成了基于氟化异恶唑支架的荧光分子,并对其光化学性质进行了研究。在3,5 - 二芳基异恶唑中引入氟取代基导致荧光强度增加,并在发射强度上呈现红移。α-氟化硼酮亚胺(F - BKIs)也通过4 - 氟异恶唑的开环反应合成,表现出高荧光发光和聚集诱导发光(AIE),有望成为一种新型荧光团。