Beilstein Journal of Organic Chemistry (Jun 2020)

Synthesis of new fluorescent molecules having an aggregation-induced emission property derived from 4-fluoroisoxazoles

  • Kazuyuki Sato,
  • Akira Kawasaki,
  • Yukiko Karuo,
  • Atsushi Tarui,
  • Kentaro Kawai,
  • Masaaki Omote

DOI
https://doi.org/10.3762/bjoc.16.117
Journal volume & issue
Vol. 16, no. 1
pp. 1411 – 1417

Abstract

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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.

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